Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000067-N01

SRX5554505 P-0000067-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000067-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518399 P-0000067-N01-WES P-0000067-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554506 P-0000067-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000067-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518400 P-0000067-T01-WES P-0000067-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554507 P-0000117-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000117-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518401 P-0000117-N01-WES P-0000117-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554508 P-0000117-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000117-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518402 P-0000117-T01-WES P-0000117-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554509 P-0000122-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000122-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518403 P-0000122-N01-WES P-0000122-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554510 P-0000122-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000122-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518404 P-0000122-T01-WES P-0000122-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554511 P-0000152-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000152-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518405 P-0000152-N01-WES P-0000152-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554512 P-0000152-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000152-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518407 P-0000152-T03-WES P-0000152-T03-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554513 P-0000184-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000184-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518406 P-0000184-N01-WES P-0000184-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554514 P-0000184-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000184-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518408 P-0000184-T02-WES P-0000184-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554515 P-0000236-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000236-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518410 P-0000236-N01-WES P-0000236-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554516 P-0000236-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000236-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518409 P-0000236-T01-WES P-0000236-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554517 P-0000328-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000328-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518411 P-0000328-N01-WES P-0000328-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554518 P-0000328-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000328-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518412 P-0000328-T01-WES P-0000328-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554519 P-0000375-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000375-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518413 P-0000375-N01-WES P-0000375-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554520 P-0000375-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000375-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518414 P-0000375-T02-WES P-0000375-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554521 P-0000377-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000377-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518415 P-0000377-N01-WES P-0000377-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554522 P-0000377-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000377-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518417 P-0000377-T01-WES P-0000377-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554523 P-0000377-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000377-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518416 P-0000377-T02-WES P-0000377-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554524 P-0000377-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000377-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518418 P-0000377-T03-WES P-0000377-T03-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554525 P-0000377-T04-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000377-T04 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518419 P-0000377-T04-WES P-0000377-T04-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554526 P-0000382-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000382-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518420 P-0000382-N01-WES P-0000382-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554527 P-0000382-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000382-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518421 P-0000382-T01-WES P-0000382-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554528 P-0000423-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000423-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518422 P-0000423-N01-WES P-0000423-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554529 P-0020546-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020546-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518423 P-0020546-N01-WES P-0020546-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554530 P-0020546-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020546-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518427 P-0020546-T01-WES P-0020546-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554531 P-0020547-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020547-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518424 P-0020547-N01-WES P-0020547-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554532 P-0020547-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020547-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518426 P-0020547-T01-WES P-0020547-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554533 P-0020548-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020548-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518425 P-0020548-N01-WES P-0020548-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554534 P-0020548-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020548-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518429 P-0020548-T01-WES P-0020548-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554535 P-0020550-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020550-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518430 P-0020550-N01-WES P-0020550-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554536 P-0020550-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020550-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518428 P-0020550-T01-WES P-0020550-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554537 P-0020551-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020551-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518431 P-0020551-N01-WES P-0020551-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554538 P-0020551-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020551-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518433 P-0020551-T01-WES P-0020551-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554539 P-0020552-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020552-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518432 P-0020552-N01-WES P-0020552-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554540 P-0020552-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020552-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518434 P-0020552-T01-WES P-0020552-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554541 P-0020553-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020553-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518436 P-0020553-N01-WES P-0020553-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554542 P-0020553-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020553-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518435 P-0020553-T01-WES P-0020553-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554543 P-0020554-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020554-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518437 P-0020554-N01-WES P-0020554-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554544 P-0020554-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020554-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518438 P-0020554-T01-WES P-0020554-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554545 P-0020556-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020556-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518439 P-0020556-N01-WES P-0020556-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554546 P-0020556-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020556-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518440 P-0020556-T01-WES P-0020556-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554547 P-0020558-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020558-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518441 P-0020558-N01-WES P-0020558-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554548 P-0020558-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020558-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518443 P-0020558-T01-WES P-0020558-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554549 P-0020559-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020559-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518442 P-0020559-N01-WES P-0020559-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554550 P-0020559-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020559-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518445 P-0020559-T01-WES P-0020559-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554551 P-0020560-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020560-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518444 P-0020560-N01-WES P-0020560-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554552 P-0020560-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020560-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518446 P-0020560-T01-WES P-0020560-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554553 P-0021159-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021159-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518447 P-0021159-N01-WES P-0021159-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554554 P-0021159-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021159-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518449 P-0021159-T01-WES P-0021159-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554555 P-0021168-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021168-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518450 P-0021168-N01-WES P-0021168-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554556 P-0021168-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021168-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518448 P-0021168-T01-WES P-0021168-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554557 P-0021169-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021169-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518451 P-0021169-N01-WES P-0021169-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554558 P-0021169-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021169-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518452 P-0021169-T01-WES P-0021169-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554559 P-0021172-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021172-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518453 P-0021172-N01-WES P-0021172-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554560 P-0021172-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021172-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518454 P-0021172-T01-WES P-0021172-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554561 P-0021173-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021173-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518455 P-0021173-N01-WES P-0021173-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554562 P-0021173-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021173-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518456 P-0021173-T01-WES P-0021173-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554563 P-0021174-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021174-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518457 P-0021174-N01-WES P-0021174-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554564 P-0021174-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021174-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518458 P-0021174-T01-WES P-0021174-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554565 P-0021175-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021175-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518459 P-0021175-N01-WES P-0021175-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554566 P-0021175-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021175-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518460 P-0021175-T01-WES P-0021175-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554567 P-0021176-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021176-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518461 P-0021176-N01-WES P-0021176-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554568 P-0021176-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021176-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518462 P-0021176-T01-WES P-0021176-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554569 P-0021178-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021178-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518463 P-0021178-N01-WES P-0021178-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554570 P-0021178-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021178-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518464 P-0021178-T01-WES P-0021178-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554571 P-0021179-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021179-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518466 P-0021179-N01-WES P-0021179-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554572 P-0021179-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021179-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518467 P-0021179-T01-WES P-0021179-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554573 P-0021181-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021181-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518468 P-0021181-N01-WES P-0021181-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554574 P-0021181-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021181-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518465 P-0021181-T01-WES P-0021181-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554575 P-0021182-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021182-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518469 P-0021182-N01-WES P-0021182-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554576 P-0021182-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021182-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518472 P-0021182-T01-WES P-0021182-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554577 P-0020562-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020562-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518470 P-0020562-N01-WES P-0020562-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554578 P-0020562-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020562-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518471 P-0020562-T01-WES P-0020562-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554579 P-0020566-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020566-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518473 P-0020566-N01-WES P-0020566-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554580 P-0020566-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020566-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518474 P-0020566-T01-WES P-0020566-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554581 P-0020568-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020568-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518475 P-0020568-N01-WES P-0020568-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554582 P-0020568-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020568-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518476 P-0020568-T01-WES P-0020568-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554583 P-0020569-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020569-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518477 P-0020569-N01-WES P-0020569-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554584 P-0020569-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020569-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518478 P-0020569-T01-WES P-0020569-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554585 P-0020570-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020570-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518479 P-0020570-N01-WES P-0020570-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554586 P-0020570-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020570-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518481 P-0020570-T01-WES P-0020570-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554587 P-0020571-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020571-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518480 P-0020571-N01-WES P-0020571-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554588 P-0020571-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020571-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518482 P-0020571-T01-WES P-0020571-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554589 P-0020573-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020573-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518483 P-0020573-N01-WES P-0020573-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554590 P-0020573-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020573-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518484 P-0020573-T01-WES P-0020573-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554591 P-0020575-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020575-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518485 P-0020575-N01-WES P-0020575-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554592 P-0020575-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020575-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518486 P-0020575-T01-WES P-0020575-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554593 P-0020576-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020576-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518488 P-0020576-N01-WES P-0020576-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554594 P-0020576-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020576-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518487 P-0020576-T01-WES P-0020576-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554595 P-0020577-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020577-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518489 P-0020577-N01-WES P-0020577-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554596 P-0020577-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020577-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518490 P-0020577-T01-WES P-0020577-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554597 P-0020578-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020578-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518491 P-0020578-N01-WES P-0020578-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554598 P-0020578-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020578-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518492 P-0020578-T01-WES P-0020578-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554599 P-0020580-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020580-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518494 P-0020580-N01-WES P-0020580-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554600 P-0020580-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020580-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518495 P-0020580-T01-WES P-0020580-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554601 P-0021183-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021183-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518493 P-0021183-N01-WES P-0021183-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554602 P-0021183-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021183-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518496 P-0021183-T01-WES P-0021183-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554603 P-0021184-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021184-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518497 P-0021184-N01-WES P-0021184-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554604 P-0021184-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021184-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518498 P-0021184-T01-WES P-0021184-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554605 P-0021190-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021190-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518499 P-0021190-N01-WES P-0021190-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554606 P-0021190-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021190-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518501 P-0021190-T01-WES P-0021190-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554607 P-0021191-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021191-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518500 P-0021191-N01-WES P-0021191-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554608 P-0021191-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021191-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518502 P-0021191-T01-WES P-0021191-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554609 P-0021192-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021192-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518503 P-0021192-N01-WES P-0021192-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554610 P-0021192-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021192-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518504 P-0021192-T01-WES P-0021192-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554611 P-0021193-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021193-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518505 P-0021193-N01-WES P-0021193-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554612 P-0021193-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021193-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518507 P-0021193-T01-WES P-0021193-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554613 P-0021194-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021194-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518508 P-0021194-N01-WES P-0021194-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554614 P-0021194-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021194-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518506 P-0021194-T01-WES P-0021194-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554615 P-0021195-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021195-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518509 P-0021195-N01-WES P-0021195-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554616 P-0021195-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021195-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518510 P-0021195-T01-WES P-0021195-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554617 P-0021196-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021196-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518511 P-0021196-N01-WES P-0021196-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554618 P-0021196-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021196-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518512 P-0021196-T01-WES P-0021196-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554619 P-0021197-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021197-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518513 P-0021197-N01-WES P-0021197-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554620 P-0021197-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021197-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518514 P-0021197-T01-WES P-0021197-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554621 P-0021198-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021198-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518515 P-0021198-N01-WES P-0021198-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554622 P-0021198-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021198-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518516 P-0021198-T01-WES P-0021198-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554623 P-0021199-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021199-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518517 P-0021199-N01-WES P-0021199-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554624 P-0021199-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021199-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518518 P-0021199-T01-WES P-0021199-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554625 P-0020581-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020581-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518520 P-0020581-N01-WES P-0020581-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554626 P-0020581-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020581-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518521 P-0020581-T01-WES P-0020581-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554627 P-0020583-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020583-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518522 P-0020583-N01-WES P-0020583-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554628 P-0020583-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020583-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518519 P-0020583-T01-WES P-0020583-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554629 P-0020584-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020584-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518523 P-0020584-N01-WES P-0020584-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554630 P-0020584-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020584-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518525 P-0020584-T01-WES P-0020584-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554631 P-0020586-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020586-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518526 P-0020586-N01-WES P-0020586-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554632 P-0020586-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020586-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518524 P-0020586-T01-WES P-0020586-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554633 P-0020587-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020587-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518527 P-0020587-N01-WES P-0020587-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554634 P-0020587-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020587-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518528 P-0020587-T01-WES P-0020587-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554635 P-0020587-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020587-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518530 P-0020587-T02-WES P-0020587-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554636 P-0020589-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020589-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518529 P-0020589-N01-WES P-0020589-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554637 P-0020589-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020589-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518531 P-0020589-T01-WES P-0020589-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554638 P-0020590-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020590-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518533 P-0020590-N01-WES P-0020590-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554639 P-0020590-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020590-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518532 P-0020590-T01-WES P-0020590-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554640 P-0020591-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020591-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518535 P-0020591-N01-WES P-0020591-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554641 P-0020591-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020591-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518534 P-0020591-T01-WES P-0020591-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554642 P-0020592-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020592-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518536 P-0020592-N01-WES P-0020592-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554643 P-0020592-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020592-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518537 P-0020592-T01-WES P-0020592-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554644 P-0020593-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020593-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518538 P-0020593-N01-WES P-0020593-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554645 P-0020593-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020593-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518540 P-0020593-T01-WES P-0020593-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554646 P-0020603-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020603-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518539 P-0020603-N01-WES P-0020603-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554647 P-0020603-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020603-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518541 P-0020603-T01-WES P-0020603-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554648 P-0020605-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020605-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518542 P-0020605-N01-WES P-0020605-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554649 P-0021201-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021201-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518543 P-0021201-N01-WES P-0021201-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554650 P-0021201-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021201-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518545 P-0021201-T01-WES P-0021201-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554651 P-0021202-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021202-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518546 P-0021202-N01-WES P-0021202-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554653 P-0021202-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021202-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518548 P-0021202-T01-WES P-0021202-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554654 P-0021203-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021203-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518547 P-0021203-N01-WES P-0021203-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554655 P-0021203-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021203-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518549 P-0021203-T01-WES P-0021203-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554656 P-0021204-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021204-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518550 P-0021204-N01-WES P-0021204-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554657 P-0021204-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021204-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518551 P-0021204-T01-WES P-0021204-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554658 P-0021205-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021205-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518552 P-0021205-N01-WES P-0021205-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554659 P-0021205-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021205-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518553 P-0021205-T01-WES P-0021205-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554660 P-0021206-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021206-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518554 P-0021206-N01-WES P-0021206-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554661 P-0021206-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021206-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518555 P-0021206-T01-WES P-0021206-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554662 P-0021207-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021207-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518556 P-0021207-N01-WES P-0021207-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554663 P-0021207-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021207-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518557 P-0021207-T01-WES P-0021207-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554664 P-0021208-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021208-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518559 P-0021208-N01-WES P-0021208-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554665 P-0021208-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021208-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518558 P-0021208-T01-WES P-0021208-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554666 P-0021211-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021211-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518560 P-0021211-N01-WES P-0021211-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554667 P-0021211-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021211-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518561 P-0021211-T01-WES P-0021211-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554669 P-0021212-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021212-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518563 P-0021212-N01-WES P-0021212-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554670 P-0021212-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021212-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518564 P-0021212-T01-WES P-0021212-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554671 P-0021217-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021217-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518565 P-0021217-N01-WES P-0021217-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554672 P-0021217-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021217-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518566 P-0021217-T01-WES P-0021217-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554673 P-0021218-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021218-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518567 P-0021218-N01-WES P-0021218-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554674 P-0021218-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021218-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518570 P-0021218-T01-WES P-0021218-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554675 P-0020605-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020605-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518568 P-0020605-T01-WES P-0020605-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554676 P-0020606-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020606-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518569 P-0020606-N01-WES P-0020606-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554677 P-0020606-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020606-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518571 P-0020606-T01-WES P-0020606-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554678 P-0020608-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020608-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518572 P-0020608-N01-WES P-0020608-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554679 P-0020608-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020608-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518574 P-0020608-T01-WES P-0020608-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554680 P-0020609-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020609-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518573 P-0020609-N01-WES P-0020609-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554681 P-0020609-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020609-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518575 P-0020609-T01-WES P-0020609-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554682 P-0020610-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020610-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518576 P-0020610-N01-WES P-0020610-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554684 P-0020610-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020610-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518578 P-0020610-T01-WES P-0020610-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554685 P-0020611-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020611-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518581 P-0020611-N01-WES P-0020611-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554686 P-0020611-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020611-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518579 P-0020611-T01-WES P-0020611-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554687 P-0020612-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020612-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518580 P-0020612-N01-WES P-0020612-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554688 P-0020612-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020612-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518582 P-0020612-T01-WES P-0020612-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554689 P-0020615-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020615-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518583 P-0020615-N01-WES P-0020615-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554690 P-0020615-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020615-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518584 P-0020615-T01-WES P-0020615-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554691 P-0020616-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020616-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518587 P-0020616-N01-WES P-0020616-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554692 P-0020616-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020616-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518586 P-0020616-T01-WES P-0020616-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554693 P-0020617-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020617-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518585 P-0020617-N01-WES P-0020617-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554694 P-0020617-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020617-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518588 P-0020617-T01-WES P-0020617-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554695 P-0020618-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020618-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518589 P-0020618-N01-WES P-0020618-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554696 P-0020618-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020618-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518590 P-0020618-T01-WES P-0020618-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554697 P-0020620-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020620-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518591 P-0020620-N01-WES P-0020620-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554698 P-0020620-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020620-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518594 P-0020620-T01-WES P-0020620-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554699 P-0020620-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020620-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518592 P-0020620-T02-WES P-0020620-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554700 P-0021219-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021219-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518593 P-0021219-N01-WES P-0021219-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554701 P-0021219-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021219-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518596 P-0021219-T01-WES P-0021219-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554703 P-0021220-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021220-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518597 P-0021220-N01-WES P-0021220-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554704 P-0021220-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021220-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518600 P-0021220-T01-WES P-0021220-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554705 P-0021221-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021221-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518599 P-0021221-N01-WES P-0021221-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554706 P-0021221-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021221-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518598 P-0021221-T01-WES P-0021221-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554707 P-0021222-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021222-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518601 P-0021222-N01-WES P-0021222-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554708 P-0021222-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021222-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518602 P-0021222-T01-WES P-0021222-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554709 P-0021223-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021223-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518603 P-0021223-N01-WES P-0021223-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554710 P-0021223-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021223-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518605 P-0021223-T01-WES P-0021223-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554711 P-0021225-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021225-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518604 P-0021225-N01-WES P-0021225-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554712 P-0021225-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021225-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518606 P-0021225-T01-WES P-0021225-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554713 P-0021226-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021226-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518607 P-0021226-N01-WES P-0021226-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554714 P-0021226-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021226-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518608 P-0021226-T01-WES P-0021226-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554715 P-0021227-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021227-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518609 P-0021227-N01-WES P-0021227-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554716 P-0021227-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021227-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518610 P-0021227-T01-WES P-0021227-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554717 P-0021228-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021228-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518611 P-0021228-N01-WES P-0021228-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554719 P-0021228-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021228-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518614 P-0021228-T01-WES P-0021228-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554720 P-0021229-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021229-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518612 P-0021229-N01-WES P-0021229-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554721 P-0021229-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021229-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518615 P-0021229-T01-WES P-0021229-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554722 P-0021230-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021230-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518616 P-0021230-N01-WES P-0021230-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554723 P-0021230-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021230-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518617 P-0021230-T01-WES P-0021230-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554724 P-0021233-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021233-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518618 P-0021233-N01-WES P-0021233-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554725 P-0021233-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021233-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518619 P-0021233-T01-WES P-0021233-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554726 P-0020621-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020621-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518620 P-0020621-N01-WES P-0020621-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554727 P-0020621-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020621-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518622 P-0020621-T01-WES P-0020621-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554728 P-0020623-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020623-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518621 P-0020623-N01-WES P-0020623-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554729 P-0020623-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020623-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518624 P-0020623-T01-WES P-0020623-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554730 P-0020624-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020624-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518623 P-0020624-N01-WES P-0020624-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554732 P-0020624-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020624-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518626 P-0020624-T01-WES P-0020624-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554733 P-0020624-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020624-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518627 P-0020624-T02-WES P-0020624-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554734 P-0020625-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020625-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518628 P-0020625-N01-WES P-0020625-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554735 P-0020625-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020625-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518631 P-0020625-T01-WES P-0020625-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554736 P-0020626-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020626-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518630 P-0020626-N01-WES P-0020626-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554737 P-0020626-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020626-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518629 P-0020626-T01-WES P-0020626-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554738 P-0020628-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020628-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518632 P-0020628-N01-WES P-0020628-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554739 P-0020628-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020628-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518633 P-0020628-T01-WES P-0020628-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554740 P-0020629-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020629-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518634 P-0020629-N01-WES P-0020629-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554741 P-0020629-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020629-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518635 P-0020629-T01-WES P-0020629-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554742 P-0020630-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020630-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518636 P-0020630-N01-WES P-0020630-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554743 P-0020630-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020630-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518637 P-0020630-T01-WES P-0020630-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554744 P-0020631-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020631-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518638 P-0020631-N01-WES P-0020631-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554745 P-0020631-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020631-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518640 P-0020631-T01-WES P-0020631-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554746 P-0020632-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020632-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518641 P-0020632-N01-WES P-0020632-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554748 P-0020632-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020632-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518642 P-0020632-T01-WES P-0020632-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554749 P-0020633-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020633-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518643 P-0020633-N01-WES P-0020633-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554750 P-0020633-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020633-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518644 P-0020633-T01-WES P-0020633-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554751 P-0020634-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020634-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518646 P-0020634-N01-WES P-0020634-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554752 P-0021234-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021234-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518647 P-0021234-N01-WES P-0021234-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554753 P-0021234-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021234-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518645 P-0021234-T01-WES P-0021234-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554754 P-0021235-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021235-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518648 P-0021235-N01-WES P-0021235-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554755 P-0021235-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021235-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518649 P-0021235-T01-WES P-0021235-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554756 P-0021236-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021236-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518651 P-0021236-N01-WES P-0021236-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554757 P-0021236-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021236-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518650 P-0021236-T01-WES P-0021236-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554758 P-0021237-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021237-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518652 P-0021237-N01-WES P-0021237-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554759 P-0021237-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021237-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518654 P-0021237-T01-WES P-0021237-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554760 P-0021238-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021238-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518653 P-0021238-N01-WES P-0021238-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554761 P-0021238-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021238-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518655 P-0021238-T01-WES P-0021238-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554762 P-0021239-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021239-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518658 P-0021239-N01-WES P-0021239-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554764 P-0021239-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021239-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518656 P-0021239-T01-WES P-0021239-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554765 P-0021240-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021240-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518659 P-0021240-N01-WES P-0021240-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554766 P-0021240-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021240-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4518660 P-0021240-T01-WES P-0021240-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554767 P-0021241-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021241-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518661 P-0021241-N01-WES P-0021241-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554768 P-0021241-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021241-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518662 P-0021241-T01-WES P-0021241-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554769 P-0021242-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021242-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518663 P-0021242-N01-WES P-0021242-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554770 P-0021242-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021242-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518666 P-0021242-T01-WES P-0021242-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554771 P-0021243-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021243-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518665 P-0021243-N01-WES P-0021243-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554772 P-0021243-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021243-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518664 P-0021243-T01-WES P-0021243-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554773 P-0021249-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021249-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518668 P-0021249-N01-WES P-0021249-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554774 P-0021249-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021249-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518667 P-0021249-T01-WES P-0021249-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554775 P-0021250-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021250-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518669 P-0021250-N01-WES P-0021250-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554776 P-0021250-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021250-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518670 P-0021250-T01-WES P-0021250-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554777 P-0020634-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020634-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518671 P-0020634-T01-WES P-0020634-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554778 P-0020635-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020635-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518672 P-0020635-N01-WES P-0020635-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554779 P-0020635-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020635-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518673 P-0020635-T01-WES P-0020635-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554781 P-0020636-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020636-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518674 P-0020636-N01-WES P-0020636-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554782 P-0020636-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020636-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518677 P-0020636-T01-WES P-0020636-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554783 P-0020638-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020638-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518676 P-0020638-N01-WES P-0020638-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554784 P-0020638-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020638-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518678 P-0020638-T01-WES P-0020638-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554785 P-0020639-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020639-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518679 P-0020639-N01-WES P-0020639-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554786 P-0020639-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020639-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518680 P-0020639-T01-WES P-0020639-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554787 P-0020640-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020640-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518681 P-0020640-N01-WES P-0020640-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554788 P-0020640-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020640-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518684 P-0020640-T01-WES P-0020640-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554789 P-0020641-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020641-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518683 P-0020641-N01-WES P-0020641-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554790 P-0020641-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020641-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518682 P-0020641-T01-WES P-0020641-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554791 P-0020641-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020641-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518685 P-0020641-T02-WES P-0020641-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554792 P-0020643-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020643-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518686 P-0020643-N01-WES P-0020643-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554793 P-0020643-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020643-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518687 P-0020643-T01-WES P-0020643-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554795 P-0020644-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020644-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518689 P-0020644-N01-WES P-0020644-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554796 P-0020644-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020644-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518690 P-0020644-T01-WES P-0020644-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554797 P-0020645-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020645-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518694 P-0020645-N01-WES P-0020645-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554798 P-0020645-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020645-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518693 P-0020645-T01-WES P-0020645-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554799 P-0020646-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020646-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518692 P-0020646-N01-WES P-0020646-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554800 P-0020646-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020646-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518691 P-0020646-T01-WES P-0020646-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554801 P-0020647-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020647-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518695 P-0020647-N01-WES P-0020647-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554802 P-0020647-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020647-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518696 P-0020647-T01-WES P-0020647-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554803 P-0021253-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021253-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518698 P-0021253-N01-WES P-0021253-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554804 P-0021253-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021253-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518697 P-0021253-T01-WES P-0021253-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554805 P-0021254-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021254-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518699 P-0021254-N01-WES P-0021254-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554806 P-0021254-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021254-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518700 P-0021254-T01-WES P-0021254-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554807 P-0021255-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021255-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518702 P-0021255-N01-WES P-0021255-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554809 P-0021255-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021255-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518703 P-0021255-T01-WES P-0021255-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554810 P-0021256-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021256-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518704 P-0021256-N01-WES P-0021256-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554811 P-0021256-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021256-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518705 P-0021256-T01-WES P-0021256-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554812 P-0021257-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021257-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518706 P-0021257-N01-WES P-0021257-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554813 P-0021257-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021257-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518707 P-0021257-T01-WES P-0021257-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554814 P-0021258-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021258-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518708 P-0021258-N01-WES P-0021258-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554815 P-0021258-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021258-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518709 P-0021258-T01-WES P-0021258-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554816 P-0021260-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021260-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518710 P-0021260-N01-WES P-0021260-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554817 P-0021260-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021260-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518713 P-0021260-T01-WES P-0021260-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554818 P-0021261-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021261-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518712 P-0021261-N01-WES P-0021261-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554819 P-0021261-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021261-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518711 P-0021261-T01-WES P-0021261-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554820 P-0021263-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021263-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518714 P-0021263-N01-WES P-0021263-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554822 P-0021263-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021263-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518716 P-0021263-T01-WES P-0021263-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554823 P-0021264-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021264-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518717 P-0021264-N01-WES P-0021264-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554824 P-0021264-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021264-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518718 P-0021264-T01-WES P-0021264-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554825 P-0021268-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021268-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518719 P-0021268-N01-WES P-0021268-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554826 P-0021268-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021268-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518720 P-0021268-T01-WES P-0021268-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554827 P-0021270-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021270-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518722 P-0021270-N01-WES P-0021270-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554828 P-0021270-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021270-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518721 P-0021270-T01-WES P-0021270-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554829 P-0020648-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020648-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518723 P-0020648-N01-WES P-0020648-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554830 P-0020648-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020648-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518724 P-0020648-T01-WES P-0020648-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554831 P-0020649-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020649-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518725 P-0020649-N01-WES P-0020649-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554832 P-0020649-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020649-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518726 P-0020649-T01-WES P-0020649-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554833 P-0020650-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020650-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518727 P-0020650-N01-WES P-0020650-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554834 P-0020650-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020650-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518729 P-0020650-T01-WES P-0020650-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554835 P-0020651-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020651-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518728 P-0020651-N01-WES P-0020651-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554836 P-0020651-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020651-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518730 P-0020651-T01-WES P-0020651-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554837 P-0020652-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020652-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518732 P-0020652-N01-WES P-0020652-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554838 P-0020652-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020652-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518731 P-0020652-T01-WES P-0020652-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554839 P-0020662-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020662-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518733 P-0020662-N01-WES P-0020662-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554840 P-0020662-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020662-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518736 P-0020662-T01-WES P-0020662-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554841 P-0020663-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020663-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518734 P-0020663-N01-WES P-0020663-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554842 P-0020663-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020663-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518737 P-0020663-T01-WES P-0020663-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554843 P-0020666-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020666-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518735 P-0020666-N01-WES P-0020666-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554844 P-0020666-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020666-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518738 P-0020666-T01-WES P-0020666-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554845 P-0020667-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020667-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518739 P-0020667-N01-WES P-0020667-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554846 P-0020667-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020667-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518742 P-0020667-T01-WES P-0020667-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554847 P-0020668-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020668-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518741 P-0020668-N01-WES P-0020668-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554848 P-0020668-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020668-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518740 P-0020668-T01-WES P-0020668-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554849 P-0020669-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020669-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518744 P-0020669-N01-WES P-0020669-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554850 P-0020669-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020669-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518743 P-0020669-T01-WES P-0020669-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554851 P-0020670-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020670-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518745 P-0020670-N01-WES P-0020670-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554852 P-0020670-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020670-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518746 P-0020670-T01-WES P-0020670-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554853 P-0021271-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021271-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518747 P-0021271-N01-WES P-0021271-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554854 P-0021271-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021271-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518748 P-0021271-T01-WES P-0021271-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554855 P-0021272-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021272-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518751 P-0021272-N01-WES P-0021272-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554856 P-0021272-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021272-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518749 P-0021272-T01-WES P-0021272-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554857 P-0021273-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021273-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518750 P-0021273-N01-WES P-0021273-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554858 P-0021273-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021273-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518752 P-0021273-T01-WES P-0021273-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554859 P-0021274-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021274-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518754 P-0021274-N01-WES P-0021274-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554860 P-0021274-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021274-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518753 P-0021274-T01-WES P-0021274-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554861 P-0021282-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021282-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518755 P-0021282-N01-WES P-0021282-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554862 P-0021282-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021282-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518756 P-0021282-T01-WES P-0021282-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554863 P-0021283-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021283-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518757 P-0021283-N01-WES P-0021283-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554864 P-0021283-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021283-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518758 P-0021283-T01-WES P-0021283-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554865 P-0021285-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021285-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518759 P-0021285-N01-WES P-0021285-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554866 P-0021285-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021285-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518760 P-0021285-T01-WES P-0021285-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554867 P-0021287-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021287-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518761 P-0021287-N01-WES P-0021287-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554868 P-0021287-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021287-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518763 P-0021287-T01-WES P-0021287-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554869 P-0021288-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021288-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518762 P-0021288-N01-WES P-0021288-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554870 P-0021288-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021288-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518764 P-0021288-T01-WES P-0021288-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554871 P-0021289-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021289-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518765 P-0021289-N01-WES P-0021289-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554872 P-0021289-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021289-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518766 P-0021289-T01-WES P-0021289-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554873 P-0021292-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021292-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518769 P-0021292-N01-WES P-0021292-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554874 P-0021292-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021292-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518768 P-0021292-T01-WES P-0021292-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554875 P-0021293-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021293-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518767 P-0021293-N01-WES P-0021293-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554876 P-0021293-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021293-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518770 P-0021293-T01-WES P-0021293-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554877 P-0000423-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000423-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518771 P-0000423-T02-WES P-0000423-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554878 P-0000441-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000441-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518772 P-0000441-N01-WES P-0000441-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554879 P-0000441-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000441-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518773 P-0000441-T01-WES P-0000441-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554880 P-0000441-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000441-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518774 P-0000441-T02-WES P-0000441-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554881 P-0000508-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000508-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518775 P-0000508-N01-WES P-0000508-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554882 P-0000508-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000508-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518776 P-0000508-T01-WES P-0000508-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554883 P-0000519-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000519-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518777 P-0000519-N01-WES P-0000519-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554884 P-0000519-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000519-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518778 P-0000519-T01-WES P-0000519-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554885 P-0000541-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000541-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518779 P-0000541-N01-WES P-0000541-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554886 P-0000541-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000541-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518781 P-0000541-T01-WES P-0000541-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554887 P-0000541-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000541-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518780 P-0000541-T03-WES P-0000541-T03-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554888 P-0000584-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000584-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518783 P-0000584-N01-WES P-0000584-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554889 P-0000584-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000584-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518784 P-0000584-T01-WES P-0000584-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554890 P-0000584-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000584-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518785 P-0000584-T03-WES P-0000584-T03-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554891 P-0000615-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000615-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518782 P-0000615-N01-WES P-0000615-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554892 P-0000615-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000615-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518788 P-0000615-T01-WES P-0000615-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554893 P-0000624-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000624-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518787 P-0000624-N01-WES P-0000624-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554894 P-0000624-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000624-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518786 P-0000624-T01-WES P-0000624-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554895 P-0000964-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0000964-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518789 P-0000964-N01-WES P-0000964-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554896 P-0000964-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0000964-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518790 P-0000964-T03-WES P-0000964-T03-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554897 P-0001092-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001092-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518791 P-0001092-N01-WES P-0001092-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554898 P-0001092-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001092-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518792 P-0001092-T01-WES P-0001092-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554899 P-0001136-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001136-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518793 P-0001136-N01-WES P-0001136-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554900 P-0001136-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001136-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518794 P-0001136-T01-WES P-0001136-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554901 P-0020673-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020673-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518795 P-0020673-N01-WES P-0020673-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554902 P-0020673-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020673-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518796 P-0020673-T01-WES P-0020673-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554903 P-0020675-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020675-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518798 P-0020675-N01-WES P-0020675-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554904 P-0020675-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020675-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518797 P-0020675-T01-WES P-0020675-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554905 P-0020676-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020676-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518799 P-0020676-N01-WES P-0020676-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554906 P-0020676-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020676-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518800 P-0020676-T01-WES P-0020676-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554907 P-0020677-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020677-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518801 P-0020677-N01-WES P-0020677-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554908 P-0020677-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020677-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518802 P-0020677-T01-WES P-0020677-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554909 P-0020679-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020679-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518803 P-0020679-N01-WES P-0020679-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554910 P-0020679-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020679-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518804 P-0020679-T01-WES P-0020679-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554911 P-0020681-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020681-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518805 P-0020681-N01-WES P-0020681-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554912 P-0020681-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020681-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518806 P-0020681-T01-WES P-0020681-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554913 P-0020682-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020682-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518807 P-0020682-N01-WES P-0020682-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554914 P-0020682-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020682-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518809 P-0020682-T01-WES P-0020682-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554915 P-0020684-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020684-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518808 P-0020684-N01-WES P-0020684-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554916 P-0020684-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020684-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518810 P-0020684-T01-WES P-0020684-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554917 P-0020685-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020685-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518811 P-0020685-N01-WES P-0020685-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554918 P-0020685-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020685-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518813 P-0020685-T01-WES P-0020685-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554919 P-0020686-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020686-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518812 P-0020686-N01-WES P-0020686-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554920 P-0020686-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020686-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518814 P-0020686-T01-WES P-0020686-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554921 P-0020687-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020687-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518817 P-0020687-N01-WES P-0020687-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554922 P-0020687-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020687-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518816 P-0020687-T01-WES P-0020687-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554923 P-0020688-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020688-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518815 P-0020688-N01-WES P-0020688-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554924 P-0020688-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020688-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518818 P-0020688-T01-WES P-0020688-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554925 P-0021294-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021294-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518819 P-0021294-N01-WES P-0021294-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554926 P-0021294-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021294-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518821 P-0021294-T01-WES P-0021294-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554927 P-0021295-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021295-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518820 P-0021295-N01-WES P-0021295-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554928 P-0021295-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021295-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518822 P-0021295-T01-WES P-0021295-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554929 P-0021296-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021296-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518823 P-0021296-N01-WES P-0021296-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554930 P-0021296-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021296-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518824 P-0021296-T01-WES P-0021296-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554931 P-0021297-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021297-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518825 P-0021297-N01-WES P-0021297-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554932 P-0021297-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021297-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518826 P-0021297-T01-WES P-0021297-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554933 P-0021298-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021298-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518827 P-0021298-N01-WES P-0021298-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554934 P-0021298-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021298-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518828 P-0021298-T01-WES P-0021298-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554935 P-0021301-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021301-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518830 P-0021301-N01-WES P-0021301-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554936 P-0021301-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021301-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518829 P-0021301-T01-WES P-0021301-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554937 P-0021302-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021302-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518831 P-0021302-N01-WES P-0021302-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554938 P-0021302-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021302-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518833 P-0021302-T01-WES P-0021302-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554939 P-0021303-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021303-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518832 P-0021303-N01-WES P-0021303-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554940 P-0021303-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021303-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518834 P-0021303-T01-WES P-0021303-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554941 P-0021350-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021350-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518836 P-0021350-N01-WES P-0021350-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554942 P-0021350-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021350-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518835 P-0021350-T01-WES P-0021350-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554943 P-0021409-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021409-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518837 P-0021409-N01-WES P-0021409-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554944 P-0021409-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021409-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518839 P-0021409-T01-WES P-0021409-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554945 P-0021471-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021471-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518838 P-0021471-N01-WES P-0021471-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554946 P-0021471-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021471-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518840 P-0021471-T01-WES P-0021471-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554947 P-0021532-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021532-N02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518841 P-0021532-N02-WES P-0021532-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554948 P-0021532-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021532-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518842 P-0021532-T02-WES P-0021532-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554949 P-0001183-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001183-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518843 P-0001183-N01-WES P-0001183-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554950 P-0001183-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001183-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518845 P-0001183-T01-WES P-0001183-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554951 P-0001325-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001325-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518844 P-0001325-N01-WES P-0001325-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554952 P-0001325-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001325-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518846 P-0001325-T02-WES P-0001325-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554953 P-0001417-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001417-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518850 P-0001417-N01-WES P-0001417-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554954 P-0001417-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001417-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518849 P-0001417-T01-WES P-0001417-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554955 P-0001440-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001440-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518848 P-0001440-N01-WES P-0001440-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554956 P-0001440-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001440-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518847 P-0001440-T01-WES P-0001440-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554957 P-0001449-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001449-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518851 P-0001449-N01-WES P-0001449-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554958 P-0001449-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001449-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518852 P-0001449-T02-WES P-0001449-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554959 P-0001556-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001556-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518853 P-0001556-N01-WES P-0001556-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554960 P-0001556-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001556-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518854 P-0001556-T01-WES P-0001556-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554961 P-0001635-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001635-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518855 P-0001635-N01-WES P-0001635-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554962 P-0001635-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001635-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518856 P-0001635-T01-WES P-0001635-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554963 P-0001687-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001687-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518857 P-0001687-N01-WES P-0001687-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554964 P-0001687-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001687-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518858 P-0001687-T01-WES P-0001687-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554965 P-0001721-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001721-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518859 P-0001721-N01-WES P-0001721-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554966 P-0001721-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001721-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518860 P-0001721-T01-WES P-0001721-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5554967 P-0001752-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001752-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518861 P-0001752-N01-WES P-0001752-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554968 P-0001752-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001752-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518862 P-0001752-T02-WES P-0001752-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554969 P-0001756-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001756-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518863 P-0001756-N01-WES P-0001756-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554970 P-0001756-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001756-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518864 P-0001756-T01-WES P-0001756-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554971 P-0001767-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001767-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518865 P-0001767-N01-WES P-0001767-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554972 P-0001767-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001767-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518866 P-0001767-T02-WES P-0001767-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554973 P-0020689-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020689-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518867 P-0020689-N01-WES P-0020689-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554974 P-0020689-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020689-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518868 P-0020689-T01-WES P-0020689-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554975 P-0020690-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020690-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518869 P-0020690-N01-WES P-0020690-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554976 P-0020690-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020690-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518870 P-0020690-T01-WES P-0020690-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554977 P-0020691-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020691-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518871 P-0020691-N01-WES P-0020691-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554978 P-0020691-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020691-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518872 P-0020691-T01-WES P-0020691-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554979 P-0020694-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020694-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518873 P-0020694-N01-WES P-0020694-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554980 P-0020694-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020694-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518874 P-0020694-T01-WES P-0020694-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554981 P-0020695-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020695-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518876 P-0020695-N01-WES P-0020695-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554982 P-0020695-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020695-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518875 P-0020695-T01-WES P-0020695-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554983 P-0020696-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020696-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518878 P-0020696-N01-WES P-0020696-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554984 P-0020696-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020696-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518879 P-0020696-T01-WES P-0020696-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554985 P-0020697-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020697-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518877 P-0020697-N01-WES P-0020697-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554986 P-0020697-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020697-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518880 P-0020697-T01-WES P-0020697-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554987 P-0020698-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020698-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518881 P-0020698-N01-WES P-0020698-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554988 P-0020698-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020698-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518883 P-0020698-T01-WES P-0020698-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554989 P-0020699-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020699-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518882 P-0020699-N01-WES P-0020699-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554990 P-0020699-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020699-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518884 P-0020699-T01-WES P-0020699-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554991 P-0020700-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020700-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518885 P-0020700-N01-WES P-0020700-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554992 P-0020700-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020700-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518886 P-0020700-T01-WES P-0020700-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554993 P-0020701-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020701-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518887 P-0020701-N01-WES P-0020701-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554994 P-0020701-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020701-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518888 P-0020701-T01-WES P-0020701-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554995 P-0020702-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020702-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518889 P-0020702-N01-WES P-0020702-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554996 P-0020702-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020702-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4518890 P-0020702-T01-WES P-0020702-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5554997 P-0021534-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021534-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518891 P-0021534-N01-WES P-0021534-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554998 P-0021534-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021534-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518892 P-0021534-T01-WES P-0021534-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5554999 P-0021715-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021715-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518893 P-0021715-N01-WES P-0021715-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555000 P-0021715-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021715-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518894 P-0021715-T01-WES P-0021715-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555001 P-0021742-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021742-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518895 P-0021742-N01-WES P-0021742-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555002 P-0021742-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021742-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518896 P-0021742-T01-WES P-0021742-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555003 P-0021840-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021840-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518897 P-0021840-N01-WES P-0021840-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555004 P-0021840-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021840-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518898 P-0021840-T01-WES P-0021840-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555005 P-0021939-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021939-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518899 P-0021939-N01-WES P-0021939-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555006 P-0021939-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021939-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518900 P-0021939-T01-WES P-0021939-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555007 P-0021982-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021982-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518901 P-0021982-N01-WES P-0021982-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555008 P-0021982-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021982-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518902 P-0021982-T01-WES P-0021982-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555009 P-0022244-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0022244-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518903 P-0022244-N01-WES P-0022244-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555010 P-0022244-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0022244-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518904 P-0022244-T01-WES P-0022244-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555011 P-0022249-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0022249-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518905 P-0022249-N01-WES P-0022249-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555012 P-0022249-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0022249-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518906 P-0022249-T01-WES P-0022249-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555013 P-0022408-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0022408-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518907 P-0022408-N01-WES P-0022408-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555014 P-0022408-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0022408-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518908 P-0022408-T01-WES P-0022408-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555015 P-0022995-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0022995-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518909 P-0022995-N01-WES P-0022995-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555016 P-0022995-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0022995-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4518910 P-0022995-T01-WES P-0022995-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555017 P-0023419-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0023419-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518911 P-0023419-N01-WES P-0023419-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555018 P-0023419-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0023419-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518912 P-0023419-T01-WES P-0023419-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555019 P-0023453-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0023453-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518913 P-0023453-N01-WES P-0023453-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555020 P-0023453-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0023453-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518914 P-0023453-T01-WES P-0023453-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555021 P-0001829-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001829-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518915 P-0001829-N01-WES P-0001829-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555022 P-0001829-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001829-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518916 P-0001829-T02-WES P-0001829-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555023 P-0001992-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0001992-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518917 P-0001992-N01-WES P-0001992-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555024 P-0001992-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0001992-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518918 P-0001992-T01-WES P-0001992-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555025 P-0002226-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002226-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4518919 P-0002226-N01-WES P-0002226-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555779 P-0002226-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002226-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519673 P-0002226-T01-WES P-0002226-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555780 P-0002226-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002226-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519674 P-0002226-T02-WES P-0002226-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555781 P-0002237-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002237-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519675 P-0002237-N01-WES P-0002237-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555782 P-0002237-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002237-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519676 P-0002237-T01-WES P-0002237-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555783 P-0002296-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002296-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519678 P-0002296-N01-WES P-0002296-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555784 P-0002296-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002296-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519677 P-0002296-T01-WES P-0002296-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555785 P-0002316-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002316-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519679 P-0002316-N01-WES P-0002316-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555786 P-0002316-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002316-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519681 P-0002316-T01-WES P-0002316-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555787 P-0002508-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002508-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519680 P-0002508-N01-WES P-0002508-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555788 P-0002508-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002508-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519682 P-0002508-T02-WES P-0002508-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555789 P-0002516-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002516-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519683 P-0002516-N01-WES P-0002516-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555790 P-0002516-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002516-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519684 P-0002516-T01-WES P-0002516-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555791 P-0002593-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002593-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519685 P-0002593-N01-WES P-0002593-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555792 P-0002593-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002593-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519686 P-0002593-T01-WES P-0002593-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555793 P-0002617-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002617-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519687 P-0002617-N01-WES P-0002617-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555795 P-0002617-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002617-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519689 P-0002617-T02-WES P-0002617-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555796 P-0002682-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002682-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519690 P-0002682-N01-WES P-0002682-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555797 P-0002682-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002682-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519691 P-0002682-T01-WES P-0002682-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555798 P-0002895-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002895-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519692 P-0002895-N01-WES P-0002895-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555799 P-0020703-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020703-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519693 P-0020703-N01-WES P-0020703-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555800 P-0020703-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020703-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519694 P-0020703-T01-WES P-0020703-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555801 P-0020705-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020705-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519695 P-0020705-N01-WES P-0020705-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555802 P-0020705-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020705-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519696 P-0020705-T01-WES P-0020705-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555803 P-0020717-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020717-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519697 P-0020717-N01-WES P-0020717-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555804 P-0020717-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020717-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519698 P-0020717-T01-WES P-0020717-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555805 P-0020719-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020719-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519699 P-0020719-N01-WES P-0020719-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555806 P-0020719-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020719-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519700 P-0020719-T01-WES P-0020719-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555808 P-0020720-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020720-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519701 P-0020720-N01-WES P-0020720-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555809 P-0020720-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020720-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519702 P-0020720-T01-WES P-0020720-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555810 P-0020723-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020723-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519703 P-0020723-N01-WES P-0020723-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555811 P-0020723-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020723-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519705 P-0020723-T01-WES P-0020723-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555812 P-0020725-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020725-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519704 P-0020725-N01-WES P-0020725-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555813 P-0020725-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020725-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519706 P-0020725-T01-WES P-0020725-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555814 P-0020726-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020726-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519707 P-0020726-N01-WES P-0020726-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555815 P-0020726-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020726-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519708 P-0020726-T01-WES P-0020726-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555816 P-0020727-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020727-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519711 P-0020727-N01-WES P-0020727-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555817 P-0020727-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020727-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519709 P-0020727-T01-WES P-0020727-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555818 P-0020730-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020730-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519710 P-0020730-N01-WES P-0020730-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555819 P-0020730-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020730-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519712 P-0020730-T01-WES P-0020730-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555820 P-0020731-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020731-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519713 P-0020731-N01-WES P-0020731-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555821 P-0020731-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020731-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519714 P-0020731-T01-WES P-0020731-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555822 P-0020731-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020731-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519716 P-0020731-T02-WES P-0020731-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555823 P-0020732-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020732-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519715 P-0020732-N01-WES P-0020732-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555824 P-0023682-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0023682-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519718 P-0023682-N01-WES P-0023682-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555825 P-0023682-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0023682-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519717 P-0023682-T01-WES P-0023682-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555826 P-0002895-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002895-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519719 P-0002895-T01-WES P-0002895-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555827 P-0002915-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0002915-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519720 P-0002915-N01-WES P-0002915-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555828 P-0002915-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0002915-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519722 P-0002915-T01-WES P-0002915-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555829 P-0003025-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003025-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519721 P-0003025-N01-WES P-0003025-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555830 P-0003025-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003025-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519723 P-0003025-T01-WES P-0003025-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555831 P-0003045-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003045-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519724 P-0003045-N01-WES P-0003045-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555832 P-0003045-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003045-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519725 P-0003045-T01-WES P-0003045-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555833 P-0003108-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003108-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519726 P-0003108-N01-WES P-0003108-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555834 P-0003108-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003108-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519727 P-0003108-T01-WES P-0003108-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555835 P-0003119-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003119-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519728 P-0003119-N01-WES P-0003119-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555836 P-0003119-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003119-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519729 P-0003119-T02-WES P-0003119-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555837 P-0003180-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003180-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519730 P-0003180-N01-WES P-0003180-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555838 P-0003180-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003180-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519731 P-0003180-T01-WES P-0003180-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555839 P-0003187-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003187-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519732 P-0003187-N01-WES P-0003187-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555840 P-0003187-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003187-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519733 P-0003187-T02-WES P-0003187-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555841 P-0003195-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003195-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519734 P-0003195-N01-WES P-0003195-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555842 P-0003195-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003195-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519735 P-0003195-T02-WES P-0003195-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555843 P-0003289-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003289-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519737 P-0003289-N01-WES P-0003289-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555844 P-0003289-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003289-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519736 P-0003289-T02-WES P-0003289-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555845 P-0003289-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003289-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519738 P-0003289-T03-WES P-0003289-T03-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555846 P-0003325-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003325-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519739 P-0003325-N01-WES P-0003325-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555847 P-0003325-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003325-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519740 P-0003325-T01-WES P-0003325-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555848 P-0003360-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003360-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519741 P-0003360-N01-WES P-0003360-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555849 P-0003360-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003360-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519742 P-0003360-T01-WES P-0003360-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555850 P-0020732-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020732-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519744 P-0020732-T01-WES P-0020732-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555851 P-0020733-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020733-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519743 P-0020733-N01-WES P-0020733-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555852 P-0020733-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020733-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519746 P-0020733-T01-WES P-0020733-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555853 P-0020734-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020734-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519745 P-0020734-N01-WES P-0020734-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555854 P-0020734-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020734-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519747 P-0020734-T01-WES P-0020734-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555855 P-0020735-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020735-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519748 P-0020735-N01-WES P-0020735-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555856 P-0020735-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020735-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519750 P-0020735-T01-WES P-0020735-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555857 P-0020738-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020738-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519749 P-0020738-N01-WES P-0020738-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555858 P-0020738-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020738-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519751 P-0020738-T01-WES P-0020738-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555859 P-0020739-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020739-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519752 P-0020739-N01-WES P-0020739-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555860 P-0020739-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020739-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519753 P-0020739-T01-WES P-0020739-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555861 P-0020740-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020740-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519754 P-0020740-N01-WES P-0020740-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555862 P-0020740-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020740-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519755 P-0020740-T01-WES P-0020740-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555863 P-0020746-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020746-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519756 P-0020746-N01-WES P-0020746-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555864 P-0020746-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020746-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519757 P-0020746-T01-WES P-0020746-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555865 P-0020749-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020749-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519759 P-0020749-N01-WES P-0020749-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555866 P-0020749-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020749-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519758 P-0020749-T01-WES P-0020749-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555867 P-0020750-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020750-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519760 P-0020750-N01-WES P-0020750-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555868 P-0020750-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020750-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519761 P-0020750-T01-WES P-0020750-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555869 P-0020751-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020751-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519762 P-0020751-N01-WES P-0020751-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555870 P-0020751-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020751-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519764 P-0020751-T01-WES P-0020751-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555871 P-0020752-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020752-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519765 P-0020752-N01-WES P-0020752-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555872 P-0020752-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020752-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519763 P-0020752-T01-WES P-0020752-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555873 P-0020753-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020753-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519766 P-0020753-N01-WES P-0020753-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555874 P-0003468-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003468-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519767 P-0003468-N01-WES P-0003468-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555875 P-0003468-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003468-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519768 P-0003468-T01-WES P-0003468-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555876 P-0003468-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003468-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519770 P-0003468-T02-WES P-0003468-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555877 P-0003476-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003476-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519769 P-0003476-N01-WES P-0003476-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555878 P-0003476-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003476-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519771 P-0003476-T01-WES P-0003476-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555879 P-0003647-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003647-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519773 P-0003647-N01-WES P-0003647-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555880 P-0003647-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003647-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519772 P-0003647-T01-WES P-0003647-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555881 P-0003777-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003777-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519774 P-0003777-N01-WES P-0003777-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555882 P-0003777-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003777-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4519775 P-0003777-T02-WES P-0003777-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555883 P-0003813-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003813-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519776 P-0003813-N01-WES P-0003813-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555884 P-0003813-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003813-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519777 P-0003813-T01-WES P-0003813-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555885 P-0003816-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003816-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519778 P-0003816-N01-WES P-0003816-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555886 P-0003816-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003816-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519780 P-0003816-T01-WES P-0003816-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555887 P-0003873-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003873-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519779 P-0003873-N01-WES P-0003873-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555888 P-0003873-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003873-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519781 P-0003873-T01-WES P-0003873-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555889 P-0003936-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0003936-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519782 P-0003936-N01-WES P-0003936-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555890 P-0003936-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0003936-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519783 P-0003936-T01-WES P-0003936-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555891 P-0004056-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004056-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519784 P-0004056-N01-WES P-0004056-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555892 P-0004056-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004056-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519785 P-0004056-T01-WES P-0004056-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555893 P-0004063-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004063-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519786 P-0004063-N01-WES P-0004063-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555894 P-0004063-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004063-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519787 P-0004063-T01-WES P-0004063-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555895 P-0004136-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004136-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519788 P-0004136-N01-WES P-0004136-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555896 P-0004136-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004136-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519789 P-0004136-T01-WES P-0004136-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555897 P-0004158-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004158-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519791 P-0004158-N01-WES P-0004158-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555898 P-0020753-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020753-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519790 P-0020753-T01-WES P-0020753-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555899 P-0020754-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020754-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519792 P-0020754-N01-WES P-0020754-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555900 P-0020754-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020754-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519793 P-0020754-T01-WES P-0020754-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555901 P-0020756-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020756-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519795 P-0020756-N01-WES P-0020756-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555902 P-0020756-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020756-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519794 P-0020756-T01-WES P-0020756-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555903 P-0020757-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020757-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519796 P-0020757-N01-WES P-0020757-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555904 P-0020757-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020757-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519797 P-0020757-T01-WES P-0020757-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555905 P-0020760-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020760-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519799 P-0020760-N01-WES P-0020760-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555906 P-0020760-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020760-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519798 P-0020760-T01-WES P-0020760-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555907 P-0020761-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020761-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519800 P-0020761-N01-WES P-0020761-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555908 P-0020761-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020761-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519801 P-0020761-T01-WES P-0020761-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555909 P-0020762-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020762-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519802 P-0020762-N01-WES P-0020762-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555910 P-0020762-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020762-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519803 P-0020762-T01-WES P-0020762-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555911 P-0020763-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020763-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519804 P-0020763-N01-WES P-0020763-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555912 P-0020763-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020763-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519805 P-0020763-T01-WES P-0020763-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555913 P-0020764-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020764-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519806 P-0020764-N01-WES P-0020764-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555914 P-0020764-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020764-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519808 P-0020764-T01-WES P-0020764-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555915 P-0020767-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020767-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519807 P-0020767-N01-WES P-0020767-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555916 P-0020767-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020767-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519809 P-0020767-T01-WES P-0020767-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555917 P-0020768-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020768-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519810 P-0020768-N01-WES P-0020768-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555918 P-0020768-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020768-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519811 P-0020768-T01-WES P-0020768-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555919 P-0020769-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020769-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519812 P-0020769-N01-WES P-0020769-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555920 P-0020769-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020769-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519813 P-0020769-T01-WES P-0020769-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555921 P-0020772-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020772-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519814 P-0020772-N01-WES P-0020772-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555922 P-0004158-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004158-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519815 P-0004158-T01-WES P-0004158-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555923 P-0004242-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004242-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519816 P-0004242-N01-WES P-0004242-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555924 P-0004242-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004242-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519818 P-0004242-T02-WES P-0004242-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555925 P-0004269-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004269-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519817 P-0004269-N01-WES P-0004269-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555926 P-0004269-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004269-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519819 P-0004269-T01-WES P-0004269-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555927 P-0004524-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004524-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519820 P-0004524-N01-WES P-0004524-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555928 P-0004524-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004524-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519821 P-0004524-T01-WES P-0004524-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555929 P-0004753-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004753-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519822 P-0004753-N01-WES P-0004753-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555930 P-0004753-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004753-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519823 P-0004753-T01-WES P-0004753-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555931 P-0004787-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004787-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519824 P-0004787-N01-WES P-0004787-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555932 P-0004787-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004787-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519825 P-0004787-T01-WES P-0004787-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555933 P-0004821-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004821-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519828 P-0004821-N01-WES P-0004821-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555934 P-0004821-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004821-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519826 P-0004821-T01-WES P-0004821-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555935 P-0004892-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004892-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519829 P-0004892-N01-WES P-0004892-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555936 P-0004892-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004892-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519827 P-0004892-T01-WES P-0004892-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555937 P-0004910-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004910-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519831 P-0004910-N01-WES P-0004910-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555938 P-0004910-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004910-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519830 P-0004910-T03-WES P-0004910-T03-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555939 P-0004954-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0004954-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519832 P-0004954-N01-WES P-0004954-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555940 P-0004954-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0004954-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519833 P-0004954-T02-WES P-0004954-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555941 P-0005035-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005035-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519834 P-0005035-N01-WES P-0005035-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555942 P-0005035-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005035-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519835 P-0005035-T01-WES P-0005035-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555943 P-0005084-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005084-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519836 P-0005084-N01-WES P-0005084-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555944 P-0005084-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005084-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519837 P-0005084-T02-WES P-0005084-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555945 P-0005312-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005312-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519838 P-0005312-N01-WES P-0005312-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555946 P-0020772-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020772-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519839 P-0020772-T01-WES P-0020772-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555947 P-0020773-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020773-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519840 P-0020773-N01-WES P-0020773-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555948 P-0020773-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020773-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519841 P-0020773-T01-WES P-0020773-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555949 P-0020774-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020774-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519842 P-0020774-N01-WES P-0020774-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555950 P-0020774-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020774-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519843 P-0020774-T01-WES P-0020774-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555951 P-0020775-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020775-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519844 P-0020775-N01-WES P-0020775-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555952 P-0020775-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020775-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519845 P-0020775-T01-WES P-0020775-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555953 P-0020776-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020776-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519848 P-0020776-N01-WES P-0020776-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555954 P-0020776-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020776-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519846 P-0020776-T01-WES P-0020776-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555955 P-0020777-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020777-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519847 P-0020777-N01-WES P-0020777-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555956 P-0020777-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020777-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519849 P-0020777-T01-WES P-0020777-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555957 P-0020778-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020778-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519850 P-0020778-N01-WES P-0020778-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555958 P-0020778-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020778-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519851 P-0020778-T01-WES P-0020778-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555959 P-0020781-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020781-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519852 P-0020781-N01-WES P-0020781-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555960 P-0020781-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020781-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519854 P-0020781-T01-WES P-0020781-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555961 P-0020782-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020782-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519853 P-0020782-N01-WES P-0020782-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555962 P-0020782-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020782-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519855 P-0020782-T01-WES P-0020782-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555963 P-0020783-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020783-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519856 P-0020783-N01-WES P-0020783-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555964 P-0020783-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020783-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519857 P-0020783-T01-WES P-0020783-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555965 P-0020784-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020784-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519859 P-0020784-N01-WES P-0020784-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555966 P-0020784-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020784-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519858 P-0020784-T01-WES P-0020784-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555967 P-0020791-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020791-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519860 P-0020791-N01-WES P-0020791-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555968 P-0020791-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020791-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519861 P-0020791-T01-WES P-0020791-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555969 P-0020792-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020792-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519862 P-0020792-N01-WES P-0020792-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555970 P-0005312-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005312-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519863 P-0005312-T01-WES P-0005312-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555971 P-0005313-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005313-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519864 P-0005313-N01-WES P-0005313-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555972 P-0005313-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005313-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519865 P-0005313-T02-WES P-0005313-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555973 P-0005391-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005391-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519866 P-0005391-N01-WES P-0005391-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555974 P-0005391-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005391-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519867 P-0005391-T01-WES P-0005391-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555975 P-0005584-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005584-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519869 P-0005584-N01-WES P-0005584-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555976 P-0005584-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005584-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519868 P-0005584-T01-WES P-0005584-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555977 P-0005683-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005683-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519870 P-0005683-N01-WES P-0005683-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555978 P-0005683-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005683-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519872 P-0005683-T01-WES P-0005683-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555979 P-0005688-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005688-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519871 P-0005688-N01-WES P-0005688-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5555980 P-0005688-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005688-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519873 P-0005688-T01-WES P-0005688-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555981 P-0005774-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005774-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519874 P-0005774-N01-WES P-0005774-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555982 P-0005774-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005774-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519875 P-0005774-T01-WES P-0005774-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555983 P-0005900-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005900-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519877 P-0005900-N01-WES P-0005900-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555984 P-0005900-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005900-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519878 P-0005900-T02-WES P-0005900-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555985 P-0005927-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0005927-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519876 P-0005927-N01-WES P-0005927-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555986 P-0005927-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0005927-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519879 P-0005927-T02-WES P-0005927-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555987 P-0006008-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006008-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519880 P-0006008-N01-WES P-0006008-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555988 P-0006008-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006008-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519882 P-0006008-T02-WES P-0006008-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555989 P-0006212-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006212-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519881 P-0006212-N01-WES P-0006212-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555990 P-0006212-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006212-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519884 P-0006212-T02-WES P-0006212-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555991 P-0006297-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006297-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519883 P-0006297-N01-WES P-0006297-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555992 P-0006297-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006297-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519885 P-0006297-T01-WES P-0006297-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555993 P-0006380-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006380-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519886 P-0006380-N01-WES P-0006380-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5555994 P-0020792-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020792-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519887 P-0020792-T01-WES P-0020792-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555995 P-0020793-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020793-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519888 P-0020793-N01-WES P-0020793-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555996 P-0020793-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020793-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519889 P-0020793-T01-WES P-0020793-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555997 P-0020794-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020794-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519890 P-0020794-N01-WES P-0020794-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555998 P-0020794-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020794-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519891 P-0020794-T01-WES P-0020794-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5555999 P-0020795-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020795-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519893 P-0020795-N01-WES P-0020795-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556000 P-0020795-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020795-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519892 P-0020795-T01-WES P-0020795-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556001 P-0020797-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020797-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519895 P-0020797-N01-WES P-0020797-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556002 P-0020797-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020797-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519894 P-0020797-T01-WES P-0020797-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556003 P-0020799-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020799-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519896 P-0020799-N01-WES P-0020799-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556004 P-0020799-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020799-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519897 P-0020799-T01-WES P-0020799-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556005 P-0020802-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020802-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519898 P-0020802-N01-WES P-0020802-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556006 P-0020802-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020802-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519899 P-0020802-T01-WES P-0020802-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556007 P-0020803-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020803-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519900 P-0020803-N01-WES P-0020803-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556008 P-0020803-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020803-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519901 P-0020803-T01-WES P-0020803-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556009 P-0020809-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020809-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519902 P-0020809-N01-WES P-0020809-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556010 P-0020809-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020809-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519903 P-0020809-T01-WES P-0020809-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556011 P-0020810-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020810-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519905 P-0020810-N01-WES P-0020810-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556012 P-0020810-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020810-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519904 P-0020810-T01-WES P-0020810-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556013 P-0020811-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020811-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519906 P-0020811-N01-WES P-0020811-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556014 P-0020811-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020811-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519907 P-0020811-T01-WES P-0020811-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556015 P-0020812-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020812-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519908 P-0020812-N01-WES P-0020812-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556016 P-0020812-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020812-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519909 P-0020812-T01-WES P-0020812-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556017 P-0020813-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020813-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519911 P-0020813-N01-WES P-0020813-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556018 P-0006380-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006380-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519910 P-0006380-T01-WES P-0006380-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556019 P-0006411-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006411-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519912 P-0006411-N01-WES P-0006411-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556020 P-0006411-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006411-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519915 P-0006411-T01-WES P-0006411-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556021 P-0006468-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006468-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519913 P-0006468-N01-WES P-0006468-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556022 P-0006468-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006468-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519916 P-0006468-T02-WES P-0006468-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556023 P-0006504-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006504-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519914 P-0006504-N01-WES P-0006504-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556024 P-0006504-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006504-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519917 P-0006504-T02-WES P-0006504-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556025 P-0006508-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006508-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519918 P-0006508-N01-WES P-0006508-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556026 P-0006508-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006508-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519920 P-0006508-T01-WES P-0006508-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556027 P-0006568-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006568-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519919 P-0006568-N01-WES P-0006568-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556028 P-0006568-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006568-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519921 P-0006568-T01-WES P-0006568-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556029 P-0006749-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006749-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519922 P-0006749-N01-WES P-0006749-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556030 P-0006749-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006749-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519923 P-0006749-T01-WES P-0006749-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556031 P-0006760-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006760-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519925 P-0006760-N01-WES P-0006760-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556032 P-0006760-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006760-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519924 P-0006760-T01-WES P-0006760-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556033 P-0006782-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006782-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519926 P-0006782-N01-WES P-0006782-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556034 P-0006782-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006782-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519927 P-0006782-T01-WES P-0006782-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556035 P-0006782-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006782-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519928 P-0006782-T02-WES P-0006782-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556036 P-0006838-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006838-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519929 P-0006838-N01-WES P-0006838-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556037 P-0006838-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006838-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519930 P-0006838-T01-WES P-0006838-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556038 P-0006840-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006840-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519932 P-0006840-N01-WES P-0006840-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556039 P-0006840-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006840-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519931 P-0006840-T01-WES P-0006840-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556040 P-0006953-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0006953-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519934 P-0006953-N01-WES P-0006953-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556041 P-0006953-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0006953-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519933 P-0006953-T01-WES P-0006953-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556042 P-0020813-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020813-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519935 P-0020813-T01-WES P-0020813-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556043 P-0020815-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020815-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519936 P-0020815-N01-WES P-0020815-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556044 P-0020815-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020815-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519937 P-0020815-T01-WES P-0020815-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556045 P-0020816-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020816-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519938 P-0020816-N01-WES P-0020816-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556046 P-0020816-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020816-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519940 P-0020816-T01-WES P-0020816-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556047 P-0020817-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020817-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519939 P-0020817-N01-WES P-0020817-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556048 P-0020817-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020817-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519941 P-0020817-T01-WES P-0020817-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556049 P-0020818-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020818-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519942 P-0020818-N01-WES P-0020818-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556050 P-0020818-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020818-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519943 P-0020818-T01-WES P-0020818-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556051 P-0020819-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020819-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519944 P-0020819-N01-WES P-0020819-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556052 P-0020819-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020819-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519945 P-0020819-T01-WES P-0020819-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556053 P-0020821-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020821-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519946 P-0020821-N01-WES P-0020821-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556054 P-0020821-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020821-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519947 P-0020821-T01-WES P-0020821-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556055 P-0020822-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020822-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519949 P-0020822-N01-WES P-0020822-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556056 P-0020822-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020822-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519948 P-0020822-T01-WES P-0020822-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556057 P-0020823-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020823-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519950 P-0020823-N01-WES P-0020823-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556058 P-0020823-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020823-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519951 P-0020823-T01-WES P-0020823-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556059 P-0020823-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020823-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519952 P-0020823-T02-WES P-0020823-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556060 P-0020824-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020824-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519953 P-0020824-N01-WES P-0020824-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556061 P-0020824-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020824-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519954 P-0020824-T01-WES P-0020824-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556062 P-0020825-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020825-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519955 P-0020825-N01-WES P-0020825-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556063 P-0020825-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020825-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519956 P-0020825-T01-WES P-0020825-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556064 P-0020826-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020826-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519957 P-0020826-N01-WES P-0020826-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556065 P-0020826-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020826-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519958 P-0020826-T01-WES P-0020826-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556066 P-0007037-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007037-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519959 P-0007037-N01-WES P-0007037-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556067 P-0007037-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007037-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519960 P-0007037-T01-WES P-0007037-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556068 P-0007104-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007104-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519961 P-0007104-N01-WES P-0007104-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556069 P-0007104-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007104-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519962 P-0007104-T02-WES P-0007104-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556070 P-0007231-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007231-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519963 P-0007231-N01-WES P-0007231-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556071 P-0007231-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007231-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519964 P-0007231-T02-WES P-0007231-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556072 P-0007298-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007298-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519967 P-0007298-N01-WES P-0007298-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556073 P-0007298-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007298-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519965 P-0007298-T02-WES P-0007298-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556074 P-0007343-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007343-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519966 P-0007343-N01-WES P-0007343-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556075 P-0007343-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007343-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519968 P-0007343-T01-WES P-0007343-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556076 P-0007354-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007354-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519969 P-0007354-N01-WES P-0007354-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556077 P-0007354-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007354-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519970 P-0007354-T01-WES P-0007354-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556078 P-0007366-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007366-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519972 P-0007366-N01-WES P-0007366-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556079 P-0007366-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007366-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519971 P-0007366-T01-WES P-0007366-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556080 P-0007515-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007515-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519973 P-0007515-N01-WES P-0007515-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556081 P-0007515-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007515-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519975 P-0007515-T01-WES P-0007515-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556082 P-0007529-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007529-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519974 P-0007529-N01-WES P-0007529-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556083 P-0007529-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007529-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519976 P-0007529-T01-WES P-0007529-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556084 P-0007531-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007531-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519977 P-0007531-N01-WES P-0007531-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556085 P-0007531-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007531-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4519978 P-0007531-T01-WES P-0007531-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556086 P-0007604-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007604-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519979 P-0007604-N01-WES P-0007604-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556087 P-0007604-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007604-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519980 P-0007604-T01-WES P-0007604-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556088 P-0007679-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007679-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519981 P-0007679-N01-WES P-0007679-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556089 P-0007679-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007679-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4519982 P-0007679-T01-WES P-0007679-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556090 P-0020827-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020827-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519983 P-0020827-N01-WES P-0020827-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556091 P-0020827-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020827-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519985 P-0020827-T01-WES P-0020827-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556092 P-0020828-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020828-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519984 P-0020828-N01-WES P-0020828-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556093 P-0020828-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020828-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519986 P-0020828-T01-WES P-0020828-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556094 P-0020829-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020829-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519987 P-0020829-N01-WES P-0020829-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556095 P-0020829-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020829-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519989 P-0020829-T01-WES P-0020829-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556096 P-0020830-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020830-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519988 P-0020830-N01-WES P-0020830-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556097 P-0020830-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020830-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519990 P-0020830-T01-WES P-0020830-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556098 P-0020831-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020831-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519991 P-0020831-N01-WES P-0020831-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556099 P-0020831-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020831-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519992 P-0020831-T01-WES P-0020831-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556100 P-0020832-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020832-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519993 P-0020832-N01-WES P-0020832-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556101 P-0020832-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020832-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519994 P-0020832-T01-WES P-0020832-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556102 P-0020833-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020833-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519997 P-0020833-N01-WES P-0020833-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556103 P-0020833-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020833-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519995 P-0020833-T01-WES P-0020833-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556104 P-0020834-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020834-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519998 P-0020834-N01-WES P-0020834-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556105 P-0020834-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020834-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519996 P-0020834-T01-WES P-0020834-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556106 P-0020835-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020835-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4519999 P-0020835-N01-WES P-0020835-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556107 P-0020835-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020835-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520000 P-0020835-T01-WES P-0020835-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556108 P-0020835-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020835-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520001 P-0020835-T02-WES P-0020835-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556109 P-0020836-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020836-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520002 P-0020836-N01-WES P-0020836-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556110 P-0020836-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020836-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520003 P-0020836-T01-WES P-0020836-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556111 P-0020837-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020837-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520004 P-0020837-N01-WES P-0020837-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556112 P-0020837-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020837-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520005 P-0020837-T01-WES P-0020837-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556113 P-0020839-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020839-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520007 P-0020839-N01-WES P-0020839-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556114 P-0007887-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007887-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520006 P-0007887-N01-WES P-0007887-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556115 P-0007887-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007887-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520008 P-0007887-T02-WES P-0007887-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556116 P-0007916-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0007916-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520009 P-0007916-N01-WES P-0007916-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556117 P-0007916-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0007916-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520010 P-0007916-T01-WES P-0007916-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556118 P-0008055-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008055-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520011 P-0008055-N01-WES P-0008055-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556119 P-0008055-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008055-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520013 P-0008055-T02-WES P-0008055-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556120 P-0008355-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008355-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520014 P-0008355-N01-WES P-0008355-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556121 P-0008355-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008355-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520012 P-0008355-T01-WES P-0008355-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556122 P-0008371-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008371-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520015 P-0008371-N01-WES P-0008371-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556123 P-0008371-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008371-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520017 P-0008371-T01-WES P-0008371-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556124 P-0008417-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008417-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520016 P-0008417-N01-WES P-0008417-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556125 P-0008417-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008417-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520018 P-0008417-T02-WES P-0008417-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556126 P-0008419-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008419-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520019 P-0008419-N01-WES P-0008419-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556127 P-0008419-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008419-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520020 P-0008419-T01-WES P-0008419-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556128 P-0008423-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008423-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520021 P-0008423-N01-WES P-0008423-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556129 P-0008423-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008423-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520022 P-0008423-T02-WES P-0008423-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556130 P-0008466-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008466-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520024 P-0008466-N01-WES P-0008466-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556131 P-0008466-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008466-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520023 P-0008466-T01-WES P-0008466-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556132 P-0008655-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008655-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520026 P-0008655-N01-WES P-0008655-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556133 P-0008655-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008655-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520025 P-0008655-T01-WES P-0008655-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556134 P-0008928-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008928-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520027 P-0008928-N01-WES P-0008928-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556135 P-0008928-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008928-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520028 P-0008928-T01-WES P-0008928-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556136 P-0008941-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008941-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520030 P-0008941-N01-WES P-0008941-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556137 P-0008941-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008941-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520031 P-0008941-T01-WES P-0008941-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556138 P-0020839-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020839-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520029 P-0020839-T01-WES P-0020839-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556139 P-0020841-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020841-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520032 P-0020841-N01-WES P-0020841-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556140 P-0020841-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020841-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520033 P-0020841-T01-WES P-0020841-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556141 P-0020842-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020842-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520034 P-0020842-N01-WES P-0020842-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556142 P-0020842-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020842-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520035 P-0020842-T01-WES P-0020842-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556143 P-0020843-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020843-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520036 P-0020843-N01-WES P-0020843-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556144 P-0020843-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020843-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520037 P-0020843-T01-WES P-0020843-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556145 P-0020846-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020846-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520039 P-0020846-N01-WES P-0020846-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556146 P-0020846-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020846-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520038 P-0020846-T01-WES P-0020846-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556147 P-0020849-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020849-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520040 P-0020849-N01-WES P-0020849-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556148 P-0020849-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020849-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520041 P-0020849-T01-WES P-0020849-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556149 P-0020850-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020850-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520043 P-0020850-N01-WES P-0020850-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556150 P-0020850-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020850-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520042 P-0020850-T01-WES P-0020850-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556151 P-0020851-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020851-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520044 P-0020851-N01-WES P-0020851-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556152 P-0020851-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020851-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520045 P-0020851-T01-WES P-0020851-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556153 P-0020860-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020860-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520048 P-0020860-N01-WES P-0020860-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556154 P-0020860-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020860-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520046 P-0020860-T01-WES P-0020860-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556155 P-0020861-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020861-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520047 P-0020861-N01-WES P-0020861-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556156 P-0020861-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020861-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520049 P-0020861-T01-WES P-0020861-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556157 P-0020862-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020862-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520051 P-0020862-N01-WES P-0020862-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556158 P-0020862-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020862-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520050 P-0020862-T01-WES P-0020862-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556159 P-0020863-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020863-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520052 P-0020863-N01-WES P-0020863-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556160 P-0020863-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020863-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520053 P-0020863-T01-WES P-0020863-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556161 P-0020864-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020864-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520055 P-0020864-N01-WES P-0020864-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556162 P-0008954-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0008954-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520054 P-0008954-N01-WES P-0008954-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556163 P-0008954-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0008954-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520056 P-0008954-T01-WES P-0008954-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556164 P-0009061-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009061-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520059 P-0009061-N01-WES P-0009061-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556165 P-0009061-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009061-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520057 P-0009061-T01-WES P-0009061-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556166 P-0009061-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009061-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520060 P-0009061-T02-WES P-0009061-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556167 P-0009090-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009090-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520058 P-0009090-N01-WES P-0009090-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556168 P-0009090-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009090-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520061 P-0009090-T01-WES P-0009090-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556169 P-0009106-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009106-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520063 P-0009106-N01-WES P-0009106-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556170 P-0009106-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009106-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520062 P-0009106-T01-WES P-0009106-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556171 P-0009270-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009270-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520064 P-0009270-N01-WES P-0009270-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556172 P-0009270-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009270-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520065 P-0009270-T01-WES P-0009270-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556173 P-0009396-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009396-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520067 P-0009396-N01-WES P-0009396-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556174 P-0009396-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009396-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520066 P-0009396-T01-WES P-0009396-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556175 P-0009423-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009423-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520068 P-0009423-N01-WES P-0009423-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556176 P-0009423-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009423-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520069 P-0009423-T02-WES P-0009423-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556177 P-0009538-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009538-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520072 P-0009538-N01-WES P-0009538-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556178 P-0009538-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009538-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520070 P-0009538-T01-WES P-0009538-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556179 P-0009601-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009601-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520073 P-0009601-N01-WES P-0009601-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556180 P-0009601-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009601-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520071 P-0009601-T01-WES P-0009601-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556181 P-0009647-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009647-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520075 P-0009647-N01-WES P-0009647-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556182 P-0009647-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009647-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520074 P-0009647-T01-WES P-0009647-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556183 P-0009654-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009654-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520076 P-0009654-N01-WES P-0009654-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556184 P-0009654-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009654-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520077 P-0009654-T01-WES P-0009654-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556185 P-0009660-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009660-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520078 P-0009660-N01-WES P-0009660-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556186 P-0020864-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020864-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520079 P-0020864-T01-WES P-0020864-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556187 P-0020865-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020865-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520080 P-0020865-N01-WES P-0020865-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556188 P-0020865-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020865-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520081 P-0020865-T01-WES P-0020865-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556189 P-0020866-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020866-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520082 P-0020866-N01-WES P-0020866-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556190 P-0020866-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020866-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520083 P-0020866-T01-WES P-0020866-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556191 P-0020867-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020867-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520084 P-0020867-N01-WES P-0020867-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556192 P-0020867-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020867-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520085 P-0020867-T01-WES P-0020867-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556193 P-0020868-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020868-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520086 P-0020868-N01-WES P-0020868-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556194 P-0020868-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020868-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520087 P-0020868-T01-WES P-0020868-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556195 P-0020869-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020869-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520088 P-0020869-N01-WES P-0020869-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556196 P-0020869-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020869-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520089 P-0020869-T01-WES P-0020869-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556197 P-0020870-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020870-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520090 P-0020870-N01-WES P-0020870-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556198 P-0020870-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020870-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520091 P-0020870-T01-WES P-0020870-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556199 P-0020871-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020871-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520092 P-0020871-N01-WES P-0020871-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556200 P-0020871-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020871-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520093 P-0020871-T01-WES P-0020871-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556201 P-0020872-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020872-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520094 P-0020872-N01-WES P-0020872-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556202 P-0020872-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020872-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520095 P-0020872-T01-WES P-0020872-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556203 P-0020874-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020874-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520096 P-0020874-N01-WES P-0020874-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556204 P-0020874-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020874-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520097 P-0020874-T01-WES P-0020874-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556205 P-0020880-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020880-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520098 P-0020880-N01-WES P-0020880-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556206 P-0020880-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020880-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520099 P-0020880-T01-WES P-0020880-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556207 P-0020881-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020881-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520100 P-0020881-N01-WES P-0020881-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556208 P-0020881-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020881-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520101 P-0020881-T01-WES P-0020881-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556209 P-0020882-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020882-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520102 P-0020882-N01-WES P-0020882-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556210 P-0009660-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009660-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520103 P-0009660-T01-WES P-0009660-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556211 P-0009700-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009700-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520104 P-0009700-N01-WES P-0009700-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556212 P-0009700-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009700-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520105 P-0009700-T02-WES P-0009700-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556213 P-0009826-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009826-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520106 P-0009826-N01-WES P-0009826-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556214 P-0009826-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009826-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520107 P-0009826-T02-WES P-0009826-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556215 P-0009875-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009875-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520108 P-0009875-N01-WES P-0009875-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556216 P-0009875-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009875-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520109 P-0009875-T01-WES P-0009875-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556217 P-0009877-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009877-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520110 P-0009877-N01-WES P-0009877-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556218 P-0009877-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009877-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520111 P-0009877-T02-WES P-0009877-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556219 P-0009923-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009923-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520112 P-0009923-N01-WES P-0009923-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556220 P-0009923-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009923-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 2500 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520113 P-0009923-T01-WES P-0009923-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556221 P-0009943-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009943-N02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520114 P-0009943-N02-WES P-0009943-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556222 P-0009943-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009943-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520115 P-0009943-T02-WES P-0009943-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556223 P-0009962-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0009962-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520116 P-0009962-N01-WES P-0009962-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556224 P-0009962-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0009962-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520117 P-0009962-T01-WES P-0009962-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556225 P-0010011-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010011-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520118 P-0010011-N01-WES P-0010011-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556226 P-0010011-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010011-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520119 P-0010011-T01-WES P-0010011-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556227 P-0010016-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010016-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520120 P-0010016-N01-WES P-0010016-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556228 P-0010016-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010016-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520121 P-0010016-T01-WES P-0010016-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556229 P-0010035-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010035-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520122 P-0010035-N01-WES P-0010035-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556230 P-0010035-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010035-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520123 P-0010035-T01-WES P-0010035-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556231 P-0010176-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010176-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520124 P-0010176-N01-WES P-0010176-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556232 P-0010176-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010176-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520125 P-0010176-T01-WES P-0010176-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556233 P-0010228-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010228-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520126 P-0010228-N01-WES P-0010228-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556234 P-0020882-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020882-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520127 P-0020882-T01-WES P-0020882-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556235 P-0020883-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020883-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520128 P-0020883-N01-WES P-0020883-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556236 P-0020883-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020883-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520129 P-0020883-T01-WES P-0020883-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556237 P-0020886-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020886-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520130 P-0020886-N01-WES P-0020886-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556238 P-0020886-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020886-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520131 P-0020886-T01-WES P-0020886-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556239 P-0020900-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020900-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520132 P-0020900-N01-WES P-0020900-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556240 P-0020900-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020900-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520133 P-0020900-T02-WES P-0020900-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556241 P-0020901-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020901-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520134 P-0020901-N01-WES P-0020901-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556242 P-0020901-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020901-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520135 P-0020901-T01-WES P-0020901-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556243 P-0020902-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020902-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520136 P-0020902-N01-WES P-0020902-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556244 P-0020902-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020902-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520137 P-0020902-T01-WES P-0020902-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556245 P-0020903-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020903-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520138 P-0020903-N01-WES P-0020903-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556246 P-0020903-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020903-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520139 P-0020903-T01-WES P-0020903-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556247 P-0020904-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020904-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520140 P-0020904-N01-WES P-0020904-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556248 P-0020904-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020904-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520141 P-0020904-T01-WES P-0020904-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556249 P-0020905-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020905-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520142 P-0020905-N01-WES P-0020905-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556250 P-0020905-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020905-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520143 P-0020905-T01-WES P-0020905-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556251 P-0020906-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020906-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520144 P-0020906-N01-WES P-0020906-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556252 P-0020906-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020906-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520145 P-0020906-T01-WES P-0020906-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556253 P-0020907-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020907-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520146 P-0020907-N01-WES P-0020907-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556254 P-0020907-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020907-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520147 P-0020907-T01-WES P-0020907-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556255 P-0020908-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020908-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520148 P-0020908-N01-WES P-0020908-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556256 P-0020908-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020908-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520149 P-0020908-T01-WES P-0020908-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556257 P-0020909-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020909-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520150 P-0020909-N01-WES P-0020909-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556258 P-0010228-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010228-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520151 P-0010228-T01-WES P-0010228-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556259 P-0010237-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010237-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520152 P-0010237-N01-WES P-0010237-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556260 P-0010237-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010237-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520153 P-0010237-T01-WES P-0010237-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556261 P-0010249-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010249-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520154 P-0010249-N01-WES P-0010249-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556262 P-0010249-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010249-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520155 P-0010249-T01-WES P-0010249-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556263 P-0010457-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010457-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520156 P-0010457-N01-WES P-0010457-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556264 P-0010457-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010457-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520157 P-0010457-T01-WES P-0010457-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556265 P-0010529-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010529-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520158 P-0010529-N01-WES P-0010529-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556266 P-0010529-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010529-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520159 P-0010529-T01-WES P-0010529-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556267 P-0010690-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010690-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520160 P-0010690-N01-WES P-0010690-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556268 P-0010690-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010690-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520161 P-0010690-T01-WES P-0010690-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556269 P-0010758-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010758-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520162 P-0010758-N01-WES P-0010758-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556270 P-0010758-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010758-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520163 P-0010758-T01-WES P-0010758-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556271 P-0010865-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010865-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520164 P-0010865-N01-WES P-0010865-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556272 P-0010865-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010865-N02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520165 P-0010865-N02-WES P-0010865-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556273 P-0010865-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010865-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520166 P-0010865-T01-WES P-0010865-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556274 P-0010865-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010865-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520167 P-0010865-T02-WES P-0010865-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556275 P-0010866-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0010866-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520168 P-0010866-N01-WES P-0010866-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556276 P-0010866-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0010866-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520169 P-0010866-T01-WES P-0010866-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556277 P-0011048-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011048-N02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520170 P-0011048-N02-WES P-0011048-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556278 P-0011048-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011048-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520171 P-0011048-T02-WES P-0011048-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556279 P-0011156-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011156-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520172 P-0011156-N01-WES P-0011156-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556280 P-0011156-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011156-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520173 P-0011156-T01-WES P-0011156-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556281 P-0011185-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011185-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520174 P-0011185-N01-WES P-0011185-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556282 P-0020909-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020909-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520175 P-0020909-T01-WES P-0020909-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556283 P-0020911-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020911-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520176 P-0020911-N01-WES P-0020911-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556284 P-0020911-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020911-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520177 P-0020911-T01-WES P-0020911-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556285 P-0020912-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020912-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520178 P-0020912-N01-WES P-0020912-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556286 P-0020912-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020912-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520179 P-0020912-T01-WES P-0020912-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556287 P-0020914-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020914-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520180 P-0020914-N01-WES P-0020914-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556288 P-0020914-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020914-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520181 P-0020914-T01-WES P-0020914-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556289 P-0020919-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020919-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520182 P-0020919-N01-WES P-0020919-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556290 P-0020919-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020919-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520183 P-0020919-T01-WES P-0020919-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556291 P-0020920-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020920-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520184 P-0020920-N01-WES P-0020920-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556292 P-0020920-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020920-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520185 P-0020920-T01-WES P-0020920-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556293 P-0020921-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020921-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520186 P-0020921-N01-WES P-0020921-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556294 P-0020921-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020921-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520187 P-0020921-T01-WES P-0020921-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556295 P-0020924-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020924-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520188 P-0020924-N01-WES P-0020924-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556296 P-0020924-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020924-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520189 P-0020924-T01-WES P-0020924-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556297 P-0020925-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020925-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520190 P-0020925-N01-WES P-0020925-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556298 P-0020925-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020925-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520191 P-0020925-T01-WES P-0020925-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556299 P-0020926-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020926-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520192 P-0020926-N01-WES P-0020926-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556300 P-0020926-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020926-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520193 P-0020926-T01-WES P-0020926-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556301 P-0020927-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020927-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520194 P-0020927-N01-WES P-0020927-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556302 P-0020927-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020927-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520195 P-0020927-T01-WES P-0020927-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556303 P-0020928-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020928-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520196 P-0020928-N01-WES P-0020928-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556304 P-0020928-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020928-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520197 P-0020928-T01-WES P-0020928-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556305 P-0020929-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020929-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520198 P-0020929-N01-WES P-0020929-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556306 P-0011185-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011185-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520199 P-0011185-T01-WES P-0011185-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556307 P-0011208-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011208-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520200 P-0011208-N01-WES P-0011208-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556308 P-0011208-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011208-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520201 P-0011208-T01-WES P-0011208-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556309 P-0011369-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011369-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520202 P-0011369-N01-WES P-0011369-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556310 P-0011369-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011369-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520203 P-0011369-T01-WES P-0011369-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556311 P-0011414-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011414-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520204 P-0011414-N01-WES P-0011414-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556312 P-0011414-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011414-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520205 P-0011414-T01-WES P-0011414-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556313 P-0011529-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011529-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520206 P-0011529-N01-WES P-0011529-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556314 P-0011529-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011529-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520207 P-0011529-T01-WES P-0011529-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556315 P-0011554-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011554-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520208 P-0011554-N01-WES P-0011554-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556316 P-0011554-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011554-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520209 P-0011554-T01-WES P-0011554-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556317 P-0011567-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0011567-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520210 P-0011567-N01-WES P-0011567-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556318 P-0011567-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0011567-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520211 P-0011567-T02-WES P-0011567-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556319 P-0012046-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012046-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520212 P-0012046-N01-WES P-0012046-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556320 P-0012046-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012046-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520213 P-0012046-T01-WES P-0012046-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556321 P-0012081-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012081-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520214 P-0012081-N01-WES P-0012081-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556322 P-0012081-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012081-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520215 P-0012081-T02-WES P-0012081-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556323 P-0012104-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012104-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4520216 P-0012104-N01-WES P-0012104-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556324 P-0012104-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012104-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4520217 P-0012104-T02-WES P-0012104-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556325 P-0012105-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012105-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520218 P-0012105-N01-WES P-0012105-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556326 P-0012105-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012105-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520219 P-0012105-T01-WES P-0012105-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556327 P-0012132-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012132-N02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520220 P-0012132-N02-WES P-0012132-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556328 P-0012132-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012132-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520221 P-0012132-T02-WES P-0012132-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556329 P-0012143-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012143-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520222 P-0012143-N01-WES P-0012143-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556330 P-0020929-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020929-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520223 P-0020929-T01-WES P-0020929-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556331 P-0020930-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020930-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520224 P-0020930-N01-WES P-0020930-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556332 P-0020930-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020930-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520225 P-0020930-T01-WES P-0020930-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556333 P-0020935-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020935-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520226 P-0020935-N01-WES P-0020935-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556334 P-0020935-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020935-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520227 P-0020935-T01-WES P-0020935-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556335 P-0020936-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020936-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520228 P-0020936-N01-WES P-0020936-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556336 P-0020936-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020936-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520229 P-0020936-T01-WES P-0020936-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556337 P-0020937-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020937-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520230 P-0020937-N01-WES P-0020937-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556338 P-0020937-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020937-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520231 P-0020937-T01-WES P-0020937-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556339 P-0020939-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020939-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520232 P-0020939-N01-WES P-0020939-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556340 P-0020939-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020939-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520233 P-0020939-T01-WES P-0020939-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556341 P-0020941-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020941-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520234 P-0020941-N01-WES P-0020941-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556342 P-0020941-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020941-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520235 P-0020941-T01-WES P-0020941-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556343 P-0020944-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020944-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520236 P-0020944-N01-WES P-0020944-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556344 P-0020944-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020944-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520237 P-0020944-T01-WES P-0020944-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556345 P-0020945-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020945-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520238 P-0020945-N01-WES P-0020945-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556346 P-0020945-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020945-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520239 P-0020945-T01-WES P-0020945-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556347 P-0020946-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020946-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520240 P-0020946-N01-WES P-0020946-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556348 P-0020946-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020946-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520241 P-0020946-T01-WES P-0020946-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556349 P-0020947-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020947-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520242 P-0020947-N01-WES P-0020947-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556350 P-0020947-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020947-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520243 P-0020947-T01-WES P-0020947-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556351 P-0020948-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020948-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520244 P-0020948-N01-WES P-0020948-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556352 P-0020948-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020948-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520245 P-0020948-T01-WES P-0020948-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556353 P-0020949-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020949-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520246 P-0020949-N01-WES P-0020949-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556354 P-0012143-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012143-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520247 P-0012143-T01-WES P-0012143-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556355 P-0012241-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012241-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520248 P-0012241-N01-WES P-0012241-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556356 P-0012241-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012241-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520249 P-0012241-T02-WES P-0012241-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556357 P-0012271-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012271-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520250 P-0012271-N01-WES P-0012271-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556358 P-0012271-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012271-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520251 P-0012271-T01-WES P-0012271-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556359 P-0012325-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012325-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520252 P-0012325-N01-WES P-0012325-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556360 P-0012325-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012325-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520253 P-0012325-T02-WES P-0012325-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556361 P-0012334-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012334-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520254 P-0012334-N01-WES P-0012334-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556362 P-0012334-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012334-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520255 P-0012334-T01-WES P-0012334-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556363 P-0012358-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012358-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520256 P-0012358-N01-WES P-0012358-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556364 P-0012358-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012358-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520257 P-0012358-T01-WES P-0012358-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556365 P-0012379-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012379-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520258 P-0012379-N01-WES P-0012379-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556366 P-0012379-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012379-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520259 P-0012379-T01-WES P-0012379-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556367 P-0012415-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012415-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520260 P-0012415-N01-WES P-0012415-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556368 P-0012415-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012415-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520261 P-0012415-T01-WES P-0012415-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556369 P-0012505-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012505-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520263 P-0012505-N01-WES P-0012505-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556370 P-0012505-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012505-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520262 P-0012505-T01-WES P-0012505-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556371 P-0012556-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012556-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520264 P-0012556-N01-WES P-0012556-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556372 P-0012556-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012556-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520265 P-0012556-T01-WES P-0012556-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556373 P-0012572-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012572-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520266 P-0012572-N01-WES P-0012572-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556374 P-0012572-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012572-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520267 P-0012572-T01-WES P-0012572-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556375 P-0012605-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012605-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520268 P-0012605-N01-WES P-0012605-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556376 P-0012605-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012605-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520269 P-0012605-T01-WES P-0012605-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556377 P-0012777-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0012777-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520270 P-0012777-N01-WES P-0012777-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556378 P-0020949-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020949-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520271 P-0020949-T01-WES P-0020949-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556379 P-0020951-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020951-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520272 P-0020951-N01-WES P-0020951-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556380 P-0020951-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020951-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520273 P-0020951-T01-WES P-0020951-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556381 P-0020952-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020952-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520274 P-0020952-N01-WES P-0020952-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556382 P-0020952-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020952-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520276 P-0020952-T01-WES P-0020952-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556383 P-0020953-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020953-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520275 P-0020953-N01-WES P-0020953-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556384 P-0020953-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020953-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520278 P-0020953-T01-WES P-0020953-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556385 P-0020953-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020953-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520277 P-0020953-T02-WES P-0020953-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556386 P-0020954-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020954-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520279 P-0020954-N01-WES P-0020954-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556387 P-0020954-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020954-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520280 P-0020954-T01-WES P-0020954-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556388 P-0020956-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020956-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520282 P-0020956-N01-WES P-0020956-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556389 P-0020956-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020956-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520281 P-0020956-T01-WES P-0020956-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556390 P-0020957-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020957-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520284 P-0020957-N01-WES P-0020957-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556391 P-0020957-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020957-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520283 P-0020957-T01-WES P-0020957-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556392 P-0020958-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020958-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520286 P-0020958-N01-WES P-0020958-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556393 P-0020958-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020958-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520285 P-0020958-T01-WES P-0020958-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556394 P-0020960-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020960-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520287 P-0020960-N01-WES P-0020960-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556395 P-0020960-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020960-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520288 P-0020960-T01-WES P-0020960-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556396 P-0020961-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020961-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520289 P-0020961-N01-WES P-0020961-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556397 P-0020961-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020961-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520290 P-0020961-T01-WES P-0020961-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556398 P-0020963-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020963-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520291 P-0020963-N01-WES P-0020963-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556399 P-0020963-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020963-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520292 P-0020963-T01-WES P-0020963-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556400 P-0020964-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020964-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520293 P-0020964-N01-WES P-0020964-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556401 P-0020964-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020964-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520294 P-0020964-T01-WES P-0020964-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556402 P-0012777-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0012777-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520295 P-0012777-T01-WES P-0012777-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556403 P-0013196-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013196-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520296 P-0013196-N01-WES P-0013196-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556404 P-0013196-T04-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013196-T04 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520297 P-0013196-T04-WES P-0013196-T04-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556405 P-0013293-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013293-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520298 P-0013293-N01-WES P-0013293-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556406 P-0013293-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013293-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520299 P-0013293-T02-WES P-0013293-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556407 P-0013303-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013303-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520300 P-0013303-N01-WES P-0013303-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556408 P-0013303-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013303-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520301 P-0013303-T01-WES P-0013303-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556409 P-0013371-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013371-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520303 P-0013371-N01-WES P-0013371-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556410 P-0013371-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013371-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520302 P-0013371-T01-WES P-0013371-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556411 P-0013503-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013503-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520304 P-0013503-N01-WES P-0013503-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556412 P-0013503-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013503-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520305 P-0013503-T02-WES P-0013503-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556413 P-0013565-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013565-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520306 P-0013565-N01-WES P-0013565-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556414 P-0013565-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013565-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520307 P-0013565-T01-WES P-0013565-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556415 P-0013837-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013837-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520308 P-0013837-N01-WES P-0013837-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556416 P-0013837-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013837-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520309 P-0013837-T01-WES P-0013837-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556417 P-0013849-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0013849-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520310 P-0013849-N01-WES P-0013849-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556418 P-0013849-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0013849-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520311 P-0013849-T02-WES P-0013849-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556419 P-0014040-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014040-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520312 P-0014040-N01-WES P-0014040-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556420 P-0014040-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014040-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520313 P-0014040-T01-WES P-0014040-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556421 P-0014144-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014144-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520314 P-0014144-N01-WES P-0014144-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556422 P-0014144-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014144-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520315 P-0014144-T01-WES P-0014144-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556423 P-0014232-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014232-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520316 P-0014232-N01-WES P-0014232-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556424 P-0014232-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014232-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520317 P-0014232-T02-WES P-0014232-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556425 P-0014408-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014408-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520318 P-0014408-N01-WES P-0014408-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556426 P-0020965-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020965-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520320 P-0020965-N01-WES P-0020965-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556427 P-0020965-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020965-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520319 P-0020965-T01-WES P-0020965-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556428 P-0020966-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020966-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520321 P-0020966-N01-WES P-0020966-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556429 P-0020966-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020966-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520322 P-0020966-T01-WES P-0020966-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556430 P-0020969-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020969-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520323 P-0020969-N01-WES P-0020969-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556431 P-0020969-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020969-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520324 P-0020969-T01-WES P-0020969-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556432 P-0020972-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020972-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520325 P-0020972-N01-WES P-0020972-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556433 P-0020972-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020972-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520326 P-0020972-T01-WES P-0020972-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556434 P-0020973-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020973-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520327 P-0020973-N01-WES P-0020973-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556435 P-0020973-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020973-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520328 P-0020973-T01-WES P-0020973-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556436 P-0020974-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020974-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520329 P-0020974-N01-WES P-0020974-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556437 P-0020974-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020974-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520330 P-0020974-T01-WES P-0020974-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556438 P-0020976-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020976-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520331 P-0020976-N01-WES P-0020976-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556439 P-0020976-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020976-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520332 P-0020976-T01-WES P-0020976-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556440 P-0020977-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020977-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520333 P-0020977-N01-WES P-0020977-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556441 P-0020977-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020977-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520334 P-0020977-T01-WES P-0020977-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556442 P-0020985-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020985-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520335 P-0020985-N01-WES P-0020985-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556443 P-0020985-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020985-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520336 P-0020985-T01-WES P-0020985-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556444 P-0020986-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020986-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520337 P-0020986-N01-WES P-0020986-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556445 P-0020986-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020986-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520338 P-0020986-T01-WES P-0020986-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556446 P-0020987-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020987-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520339 P-0020987-N01-WES P-0020987-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556447 P-0020987-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020987-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520340 P-0020987-T01-WES P-0020987-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556448 P-0020989-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020989-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520341 P-0020989-N01-WES P-0020989-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556449 P-0020989-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020989-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520342 P-0020989-T01-WES P-0020989-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556450 P-0014408-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014408-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520343 P-0014408-T01-WES P-0014408-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556451 P-0014421-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014421-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520344 P-0014421-N01-WES P-0014421-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556452 P-0014421-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014421-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520345 P-0014421-T01-WES P-0014421-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556453 P-0014435-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014435-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520346 P-0014435-N01-WES P-0014435-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556454 P-0014435-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014435-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520347 P-0014435-T01-WES P-0014435-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556455 P-0014435-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014435-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520348 P-0014435-T02-WES P-0014435-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556456 P-0014501-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014501-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4520349 P-0014501-N01-WES P-0014501-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556457 P-0014501-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014501-T02 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 4000,Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit." SRS4520350 P-0014501-T02-WES P-0014501-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556458 P-0014574-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014574-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520351 P-0014574-N01-WES P-0014574-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556459 P-0014574-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014574-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520352 P-0014574-T01-WES P-0014574-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556461 P-0014594-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014594-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520354 P-0014594-T01-WES P-0014594-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556462 P-0014821-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014821-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520355 P-0014821-N01-WES P-0014821-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556463 P-0014821-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014821-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520356 P-0014821-T02-WES P-0014821-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556464 P-0014885-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0014885-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520357 P-0014885-N01-WES P-0014885-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556465 P-0014885-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0014885-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520358 P-0014885-T02-WES P-0014885-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556466 P-0015095-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015095-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520360 P-0015095-N01-WES P-0015095-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556467 P-0015095-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015095-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520359 P-0015095-T01-WES P-0015095-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556468 P-0015131-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015131-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520361 P-0015131-N01-WES P-0015131-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556469 P-0015131-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015131-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520362 P-0015131-T01-WES P-0015131-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556470 P-0015138-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015138-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520363 P-0015138-N01-WES P-0015138-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556471 P-0015138-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015138-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520364 P-0015138-T01-WES P-0015138-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556472 P-0015255-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015255-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520365 P-0015255-N01-WES P-0015255-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556473 P-0015255-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015255-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520366 P-0015255-T01-WES P-0015255-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556474 P-0020991-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020991-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520367 P-0020991-N01-WES P-0020991-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556475 P-0020991-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020991-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520368 P-0020991-T01-WES P-0020991-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556476 P-0020992-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020992-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520369 P-0020992-N01-WES P-0020992-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556477 P-0020992-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020992-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520370 P-0020992-T01-WES P-0020992-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556478 P-0020994-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020994-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520371 P-0020994-N01-WES P-0020994-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556479 P-0020994-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020994-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520372 P-0020994-T01-WES P-0020994-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556480 P-0020995-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020995-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520373 P-0020995-N01-WES P-0020995-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556481 P-0020995-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020995-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520374 P-0020995-T01-WES P-0020995-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556482 P-0020997-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020997-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520375 P-0020997-N01-WES P-0020997-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556483 P-0020997-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020997-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520376 P-0020997-T01-WES P-0020997-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556484 P-0020998-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020998-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520377 P-0020998-N01-WES P-0020998-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556485 P-0020998-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020998-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520378 P-0020998-T01-WES P-0020998-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556486 P-0021000-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021000-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520379 P-0021000-N01-WES P-0021000-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556487 P-0021000-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021000-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520380 P-0021000-T01-WES P-0021000-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556488 P-0021001-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021001-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520381 P-0021001-N01-WES P-0021001-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556489 P-0021001-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021001-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520382 P-0021001-T01-WES P-0021001-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556490 P-0021004-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021004-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520383 P-0021004-N01-WES P-0021004-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556491 P-0021004-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021004-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520384 P-0021004-T01-WES P-0021004-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556492 P-0021005-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021005-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520385 P-0021005-N01-WES P-0021005-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556493 P-0021005-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021005-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520386 P-0021005-T01-WES P-0021005-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556494 P-0021006-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021006-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520387 P-0021006-N01-WES P-0021006-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556495 P-0021006-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021006-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520388 P-0021006-T01-WES P-0021006-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556496 P-0021009-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021009-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520389 P-0021009-N01-WES P-0021009-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556497 P-0021009-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021009-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520390 P-0021009-T01-WES P-0021009-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556498 P-0015280-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015280-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520391 P-0015280-N01-WES P-0015280-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556499 P-0015280-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015280-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520392 P-0015280-T01-WES P-0015280-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556500 P-0015415-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015415-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520393 P-0015415-N01-WES P-0015415-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556501 P-0015415-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015415-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520394 P-0015415-T01-WES P-0015415-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556502 P-0015432-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015432-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520395 P-0015432-N01-WES P-0015432-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556503 P-0015432-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015432-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520396 P-0015432-T01-WES P-0015432-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556504 P-0015476-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015476-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520397 P-0015476-N01-WES P-0015476-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556505 P-0015476-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015476-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520398 P-0015476-T01-WES P-0015476-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556506 P-0015493-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015493-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520399 P-0015493-N01-WES P-0015493-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556507 P-0015493-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015493-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520400 P-0015493-T03-WES P-0015493-T03-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556508 P-0015537-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015537-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520401 P-0015537-N01-WES P-0015537-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556509 P-0015537-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015537-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520402 P-0015537-T01-WES P-0015537-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556510 P-0015564-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015564-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520403 P-0015564-N01-WES P-0015564-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556511 P-0015564-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015564-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520404 P-0015564-T01-WES P-0015564-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556512 P-0015628-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015628-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520405 P-0015628-N01-WES P-0015628-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556513 P-0015628-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015628-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520406 P-0015628-T01-WES P-0015628-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556514 P-0015672-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015672-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520407 P-0015672-N01-WES P-0015672-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556515 P-0015672-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015672-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520408 P-0015672-T01-WES P-0015672-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556516 P-0015674-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015674-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520409 P-0015674-N01-WES P-0015674-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556517 P-0015674-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015674-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520410 P-0015674-T01-WES P-0015674-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556518 P-0015828-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015828-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520411 P-0015828-N01-WES P-0015828-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556519 P-0015828-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015828-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520412 P-0015828-T01-WES P-0015828-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556520 P-0015866-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0015866-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520413 P-0015866-N01-WES P-0015866-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556521 P-0015866-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0015866-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520414 P-0015866-T01-WES P-0015866-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556522 P-0021012-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021012-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520415 P-0021012-N01-WES P-0021012-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556523 P-0021012-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021012-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520416 P-0021012-T01-WES P-0021012-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556524 P-0021013-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021013-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520417 P-0021013-N01-WES P-0021013-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556525 P-0021013-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021013-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520418 P-0021013-T01-WES P-0021013-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556526 P-0021014-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021014-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520419 P-0021014-N01-WES P-0021014-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556527 P-0021014-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021014-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520420 P-0021014-T01-WES P-0021014-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556528 P-0021022-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021022-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520421 P-0021022-N01-WES P-0021022-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556529 P-0021022-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021022-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520422 P-0021022-T01-WES P-0021022-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556530 P-0021023-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021023-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520423 P-0021023-N01-WES P-0021023-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556531 P-0021023-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021023-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520425 P-0021023-T01-WES P-0021023-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556532 P-0021024-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021024-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520424 P-0021024-N01-WES P-0021024-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556533 P-0021024-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021024-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520426 P-0021024-T01-WES P-0021024-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556534 P-0021025-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021025-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520427 P-0021025-N01-WES P-0021025-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556535 P-0021025-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021025-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520428 P-0021025-T01-WES P-0021025-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556536 P-0021026-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021026-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520429 P-0021026-N01-WES P-0021026-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556537 P-0021026-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021026-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520430 P-0021026-T01-WES P-0021026-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556538 P-0021027-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021027-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520431 P-0021027-N01-WES P-0021027-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556539 P-0021027-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021027-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520432 P-0021027-T01-WES P-0021027-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556540 P-0021028-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021028-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520433 P-0021028-N01-WES P-0021028-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556541 P-0021028-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021028-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520434 P-0021028-T01-WES P-0021028-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556542 P-0021029-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021029-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520435 P-0021029-N01-WES P-0021029-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556543 P-0021029-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021029-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520436 P-0021029-T01-WES P-0021029-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556544 P-0021030-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021030-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520437 P-0021030-N01-WES P-0021030-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556545 P-0021030-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021030-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520438 P-0021030-T01-WES P-0021030-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556546 P-0016053-N02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016053-N02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520439 P-0016053-N02-WES P-0016053-N02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556547 P-0016053-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016053-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520440 P-0016053-T01-WES P-0016053-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556548 P-0016099-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016099-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520442 P-0016099-N01-WES P-0016099-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556549 P-0016099-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016099-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520441 P-0016099-T01-WES P-0016099-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556550 P-0016148-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016148-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520443 P-0016148-N01-WES P-0016148-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556551 P-0016148-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016148-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520444 P-0016148-T01-WES P-0016148-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556552 P-0016201-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016201-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520445 P-0016201-N01-WES P-0016201-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556553 P-0016201-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016201-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520446 P-0016201-T01-WES P-0016201-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556554 P-0016225-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016225-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520447 P-0016225-N01-WES P-0016225-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556555 P-0016225-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016225-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520449 P-0016225-T01-WES P-0016225-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556556 P-0016243-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016243-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520448 P-0016243-N01-WES P-0016243-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556557 P-0016243-T04-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016243-T04 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520450 P-0016243-T04-WES P-0016243-T04-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556558 P-0016359-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016359-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520451 P-0016359-N01-WES P-0016359-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556559 P-0016359-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016359-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520452 P-0016359-T01-WES P-0016359-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556560 P-0016423-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016423-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520453 P-0016423-N01-WES P-0016423-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556561 P-0016423-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016423-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520454 P-0016423-T03-WES P-0016423-T03-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556562 P-0016484-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016484-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520455 P-0016484-N01-WES P-0016484-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556563 P-0016484-T03-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016484-T03 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520456 P-0016484-T03-WES P-0016484-T03-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556564 P-0016518-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016518-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520457 P-0016518-N01-WES P-0016518-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556565 P-0016518-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016518-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520458 P-0016518-T02-WES P-0016518-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556566 P-0016564-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016564-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520459 P-0016564-N01-WES P-0016564-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556567 P-0016564-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016564-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520460 P-0016564-T01-WES P-0016564-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556568 P-0016638-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016638-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520462 P-0016638-N01-WES P-0016638-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556569 P-0016638-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016638-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520461 P-0016638-T02-WES P-0016638-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556570 P-0021031-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021031-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520463 P-0021031-N01-WES P-0021031-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556571 P-0021031-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021031-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520464 P-0021031-T01-WES P-0021031-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556572 P-0021032-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021032-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520465 P-0021032-N01-WES P-0021032-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556573 P-0021032-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021032-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520466 P-0021032-T01-WES P-0021032-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556574 P-0021035-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021035-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520467 P-0021035-N01-WES P-0021035-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556575 P-0021035-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021035-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520468 P-0021035-T01-WES P-0021035-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556576 P-0021036-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021036-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520469 P-0021036-N01-WES P-0021036-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556577 P-0021036-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021036-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520470 P-0021036-T01-WES P-0021036-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556578 P-0021037-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021037-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520471 P-0021037-N01-WES P-0021037-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556579 P-0021037-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021037-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520472 P-0021037-T01-WES P-0021037-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556580 P-0021038-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021038-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520473 P-0021038-N01-WES P-0021038-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556581 P-0021038-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021038-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520474 P-0021038-T01-WES P-0021038-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556582 P-0021039-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021039-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520475 P-0021039-N01-WES P-0021039-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556583 P-0021039-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021039-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520476 P-0021039-T01-WES P-0021039-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556584 P-0021040-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021040-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520477 P-0021040-N01-WES P-0021040-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556585 P-0021040-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021040-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520478 P-0021040-T01-WES P-0021040-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556586 P-0021041-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021041-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520479 P-0021041-N01-WES P-0021041-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556587 P-0021041-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021041-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520480 P-0021041-T01-WES P-0021041-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556588 P-0021042-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021042-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520481 P-0021042-N01-WES P-0021042-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556589 P-0021042-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021042-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520482 P-0021042-T01-WES P-0021042-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556590 P-0021045-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021045-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520483 P-0021045-N01-WES P-0021045-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556591 P-0021045-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021045-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520484 P-0021045-T01-WES P-0021045-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556592 P-0021046-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021046-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520485 P-0021046-N01-WES P-0021046-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556593 P-0021046-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021046-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520486 P-0021046-T01-WES P-0021046-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556594 P-0016697-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016697-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520487 P-0016697-N01-WES P-0016697-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556595 P-0016697-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016697-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520488 P-0016697-T01-WES P-0016697-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556596 P-0016768-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016768-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520489 P-0016768-N01-WES P-0016768-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556597 P-0016768-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016768-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520491 P-0016768-T01-WES P-0016768-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556598 P-0016812-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0016812-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520490 P-0016812-N01-WES P-0016812-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556599 P-0016812-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0016812-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520492 P-0016812-T01-WES P-0016812-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556600 P-0017006-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017006-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520493 P-0017006-N01-WES P-0017006-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556601 P-0017006-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017006-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520494 P-0017006-T01-WES P-0017006-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556602 P-0017068-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017068-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520495 P-0017068-N01-WES P-0017068-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556603 P-0017068-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017068-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520496 P-0017068-T01-WES P-0017068-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556604 P-0017116-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017116-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520497 P-0017116-N01-WES P-0017116-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556605 P-0017116-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017116-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520498 P-0017116-T01-WES P-0017116-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556606 P-0017154-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017154-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520499 P-0017154-N01-WES P-0017154-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556607 P-0017154-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017154-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520500 P-0017154-T02-WES P-0017154-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556608 P-0017168-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017168-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520501 P-0017168-N01-WES P-0017168-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556609 P-0017168-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017168-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520502 P-0017168-T01-WES P-0017168-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556610 P-0017169-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017169-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520503 P-0017169-N01-WES P-0017169-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556611 P-0017169-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017169-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520504 P-0017169-T01-WES P-0017169-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556612 P-0017217-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017217-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520505 P-0017217-N01-WES P-0017217-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556613 P-0017217-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017217-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520506 P-0017217-T01-WES P-0017217-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556614 P-0017309-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017309-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520507 P-0017309-N01-WES P-0017309-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556615 P-0017309-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017309-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520508 P-0017309-T01-WES P-0017309-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556616 P-0017311-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017311-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520509 P-0017311-N01-WES P-0017311-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556617 P-0017311-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017311-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520510 P-0017311-T01-WES P-0017311-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556618 P-0021047-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021047-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520511 P-0021047-N01-WES P-0021047-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556619 P-0021047-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021047-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520512 P-0021047-T01-WES P-0021047-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556620 P-0021048-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021048-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520513 P-0021048-N01-WES P-0021048-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556621 P-0021048-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021048-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520514 P-0021048-T01-WES P-0021048-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556622 P-0021049-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021049-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520515 P-0021049-N01-WES P-0021049-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556623 P-0021049-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021049-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520516 P-0021049-T01-WES P-0021049-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556624 P-0021050-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021050-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520517 P-0021050-N01-WES P-0021050-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556625 P-0021050-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021050-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520518 P-0021050-T01-WES P-0021050-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556626 P-0021051-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021051-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520519 P-0021051-N01-WES P-0021051-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556627 P-0021051-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021051-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520521 P-0021051-T01-WES P-0021051-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556628 P-0021052-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021052-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520520 P-0021052-N01-WES P-0021052-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556629 P-0021052-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021052-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520522 P-0021052-T01-WES P-0021052-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556630 P-0021053-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021053-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520523 P-0021053-N01-WES P-0021053-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556631 P-0021053-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021053-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520524 P-0021053-T01-WES P-0021053-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556632 P-0021054-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021054-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520525 P-0021054-N01-WES P-0021054-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556633 P-0021054-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021054-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520526 P-0021054-T01-WES P-0021054-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556634 P-0021056-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021056-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520527 P-0021056-N01-WES P-0021056-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556635 P-0021056-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021056-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520528 P-0021056-T01-WES P-0021056-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556636 P-0021057-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021057-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520529 P-0021057-N01-WES P-0021057-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556637 P-0021057-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021057-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520530 P-0021057-T01-WES P-0021057-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556638 P-0021058-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021058-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520531 P-0021058-N01-WES P-0021058-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556639 P-0021058-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021058-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520532 P-0021058-T01-WES P-0021058-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556640 P-0021059-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021059-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520533 P-0021059-N01-WES P-0021059-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556641 P-0021059-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021059-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520534 P-0021059-T01-WES P-0021059-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556642 P-0017365-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017365-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520536 P-0017365-N01-WES P-0017365-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556643 P-0017365-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017365-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520535 P-0017365-T02-WES P-0017365-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556644 P-0017478-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017478-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520537 P-0017478-N01-WES P-0017478-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556645 P-0017478-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017478-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520538 P-0017478-T02-WES P-0017478-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556646 P-0017524-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017524-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520539 P-0017524-N01-WES P-0017524-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556647 P-0017524-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017524-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520540 P-0017524-T01-WES P-0017524-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556648 P-0017542-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017542-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520541 P-0017542-N01-WES P-0017542-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556649 P-0017542-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017542-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520542 P-0017542-T01-WES P-0017542-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556650 P-0017760-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017760-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520543 P-0017760-N01-WES P-0017760-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556651 P-0017760-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017760-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520544 P-0017760-T01-WES P-0017760-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556652 P-0017825-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017825-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520545 P-0017825-N01-WES P-0017825-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556653 P-0017825-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017825-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520546 P-0017825-T01-WES P-0017825-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556654 P-0017842-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017842-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520547 P-0017842-N01-WES P-0017842-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556655 P-0017842-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017842-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520548 P-0017842-T02-WES P-0017842-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556656 P-0017882-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017882-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520549 P-0017882-N01-WES P-0017882-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556657 P-0017882-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017882-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520550 P-0017882-T02-WES P-0017882-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556658 P-0017920-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0017920-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520551 P-0017920-N01-WES P-0017920-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556659 P-0017920-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0017920-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520552 P-0017920-T02-WES P-0017920-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556660 P-0018086-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018086-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520553 P-0018086-N01-WES P-0018086-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556661 P-0018086-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018086-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520554 P-0018086-T01-WES P-0018086-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556662 P-0018166-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018166-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520555 P-0018166-N01-WES P-0018166-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556663 P-0018166-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018166-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520556 P-0018166-T02-WES P-0018166-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556664 P-0018413-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018413-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520557 P-0018413-N01-WES P-0018413-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556665 P-0018413-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018413-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520558 P-0018413-T01-WES P-0018413-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556666 P-0021060-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021060-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520559 P-0021060-N01-WES P-0021060-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556667 P-0021060-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021060-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520560 P-0021060-T01-WES P-0021060-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556669 P-0021061-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021061-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520562 P-0021061-N01-WES P-0021061-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556670 P-0021061-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021061-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520563 P-0021061-T01-WES P-0021061-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556671 P-0021062-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021062-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520564 P-0021062-N01-WES P-0021062-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556672 P-0021062-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021062-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520565 P-0021062-T01-WES P-0021062-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556673 P-0021063-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021063-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520566 P-0021063-N01-WES P-0021063-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556674 P-0021063-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021063-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520567 P-0021063-T01-WES P-0021063-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556675 P-0021064-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021064-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520568 P-0021064-N01-WES P-0021064-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556676 P-0021064-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021064-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520569 P-0021064-T01-WES P-0021064-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556677 P-0021065-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021065-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520570 P-0021065-N01-WES P-0021065-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556678 P-0021065-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021065-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520571 P-0021065-T01-WES P-0021065-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556679 P-0021066-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021066-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520572 P-0021066-N01-WES P-0021066-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556680 P-0021066-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021066-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520573 P-0021066-T01-WES P-0021066-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556682 P-0021067-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021067-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520575 P-0021067-N01-WES P-0021067-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556683 P-0021067-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021067-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520576 P-0021067-T01-WES P-0021067-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556684 P-0021068-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021068-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520577 P-0021068-N01-WES P-0021068-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556685 P-0021068-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021068-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520578 P-0021068-T01-WES P-0021068-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556686 P-0021069-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021069-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520579 P-0021069-N01-WES P-0021069-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556687 P-0021069-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021069-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520580 P-0021069-T01-WES P-0021069-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556688 P-0021070-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021070-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520581 P-0021070-N01-WES P-0021070-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556689 P-0021070-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021070-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520582 P-0021070-T01-WES P-0021070-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556690 P-0021071-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021071-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520583 P-0021071-N01-WES P-0021071-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556691 P-0021071-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021071-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520584 P-0021071-T01-WES P-0021071-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556692 P-0018466-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018466-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520585 P-0018466-N01-WES P-0018466-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556694 P-0018466-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018466-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520587 P-0018466-T01-WES P-0018466-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556695 P-0018514-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018514-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520589 P-0018514-N01-WES P-0018514-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556696 P-0018514-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018514-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520588 P-0018514-T01-WES P-0018514-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556697 P-0018550-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018550-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520590 P-0018550-N01-WES P-0018550-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556698 P-0018550-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018550-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520592 P-0018550-T01-WES P-0018550-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556699 P-0018605-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018605-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520591 P-0018605-N01-WES P-0018605-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556700 P-0018605-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018605-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520593 P-0018605-T01-WES P-0018605-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556701 P-0018647-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018647-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520594 P-0018647-N01-WES P-0018647-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556702 P-0018647-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018647-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520595 P-0018647-T01-WES P-0018647-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556703 P-0018696-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018696-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520597 P-0018696-N01-WES P-0018696-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556704 P-0018696-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018696-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520596 P-0018696-T02-WES P-0018696-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556705 P-0018860-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018860-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520598 P-0018860-N01-WES P-0018860-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556706 P-0018860-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018860-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520599 P-0018860-T02-WES P-0018860-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556707 P-0018913-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018913-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520600 P-0018913-N01-WES P-0018913-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556709 P-0018913-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018913-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520603 P-0018913-T02-WES P-0018913-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556710 P-0018944-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018944-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520602 P-0018944-N01-WES P-0018944-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556711 P-0018944-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018944-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520606 P-0018944-T01-WES P-0018944-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556712 P-0018996-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0018996-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520604 P-0018996-N01-WES P-0018996-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556713 P-0018996-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0018996-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520605 P-0018996-T01-WES P-0018996-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556714 P-0019007-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019007-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520607 P-0019007-N01-WES P-0019007-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556715 P-0019007-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019007-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520609 P-0019007-T01-WES P-0019007-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556716 P-0019133-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019133-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520608 P-0019133-N01-WES P-0019133-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556717 P-0019133-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019133-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520611 P-0019133-T01-WES P-0019133-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556718 P-0021072-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021072-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520610 P-0021072-N01-WES P-0021072-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556719 P-0021072-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021072-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520612 P-0021072-T01-WES P-0021072-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556720 P-0021073-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021073-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520613 P-0021073-N01-WES P-0021073-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556722 P-0021073-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021073-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520616 P-0021073-T01-WES P-0021073-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556723 P-0021075-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021075-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520615 P-0021075-N01-WES P-0021075-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556724 P-0021075-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021075-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520618 P-0021075-T01-WES P-0021075-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556725 P-0021076-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021076-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520617 P-0021076-N01-WES P-0021076-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556726 P-0021076-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021076-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520619 P-0021076-T01-WES P-0021076-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556727 P-0021077-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021077-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520620 P-0021077-N01-WES P-0021077-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556728 P-0021077-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021077-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520621 P-0021077-T01-WES P-0021077-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556729 P-0021079-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021079-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520622 P-0021079-N01-WES P-0021079-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556730 P-0021079-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021079-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520623 P-0021079-T01-WES P-0021079-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556731 P-0021080-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021080-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520624 P-0021080-N01-WES P-0021080-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556732 P-0021080-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021080-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520626 P-0021080-T01-WES P-0021080-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556733 P-0021081-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021081-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520625 P-0021081-N01-WES P-0021081-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556734 P-0021081-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021081-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520628 P-0021081-T01-WES P-0021081-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556735 P-0021082-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021082-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520627 P-0021082-N01-WES P-0021082-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556736 P-0021082-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021082-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520629 P-0021082-T01-WES P-0021082-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556737 P-0021083-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021083-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520630 P-0021083-N01-WES P-0021083-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556739 P-0021083-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021083-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520632 P-0021083-T01-WES P-0021083-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556740 P-0021089-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021089-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520633 P-0021089-N01-WES P-0021089-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556741 P-0021089-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021089-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520634 P-0021089-T01-WES P-0021089-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556742 P-0021090-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021090-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520635 P-0021090-N01-WES P-0021090-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556743 P-0021090-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021090-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520636 P-0021090-T01-WES P-0021090-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556744 P-0019325-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019325-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520637 P-0019325-N01-WES P-0019325-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556745 P-0019325-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019325-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520638 P-0019325-T01-WES P-0019325-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556746 P-0019391-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019391-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520639 P-0019391-N01-WES P-0019391-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556747 P-0019391-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019391-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520640 P-0019391-T01-WES P-0019391-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556748 P-0019667-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019667-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520641 P-0019667-N01-WES P-0019667-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556749 P-0019667-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019667-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520643 P-0019667-T01-WES P-0019667-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556750 P-0019724-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019724-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520642 P-0019724-N01-WES P-0019724-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556752 P-0019724-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019724-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520645 P-0019724-T01-WES P-0019724-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556753 P-0019731-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019731-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520646 P-0019731-N01-WES P-0019731-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556754 P-0019731-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019731-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520647 P-0019731-T01-WES P-0019731-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556755 P-0019782-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019782-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520648 P-0019782-N01-WES P-0019782-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556756 P-0019782-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019782-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520649 P-0019782-T01-WES P-0019782-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556757 P-0019793-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019793-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520650 P-0019793-N01-WES P-0019793-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556758 P-0019793-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019793-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520651 P-0019793-T02-WES P-0019793-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556759 P-0019797-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019797-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520652 P-0019797-N01-WES P-0019797-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556760 P-0019797-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019797-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520653 P-0019797-T01-WES P-0019797-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556761 P-0019804-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019804-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520654 P-0019804-N01-WES P-0019804-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556763 P-0019804-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019804-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520656 P-0019804-T02-WES P-0019804-T02-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556764 P-0019831-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019831-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520657 P-0019831-N01-WES P-0019831-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556765 P-0019831-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019831-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520658 P-0019831-T02-WES P-0019831-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556766 P-0019840-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019840-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520660 P-0019840-N01-WES P-0019840-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556767 P-0019840-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019840-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520659 P-0019840-T01-WES P-0019840-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556768 P-0019850-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019850-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520663 P-0019850-N01-WES P-0019850-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556769 P-0019850-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019850-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520661 P-0019850-T01-WES P-0019850-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556770 P-0021091-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021091-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520662 P-0021091-N01-WES P-0021091-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556771 P-0021091-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021091-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520665 P-0021091-T01-WES P-0021091-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556772 P-0021093-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021093-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520664 P-0021093-N01-WES P-0021093-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556773 P-0021093-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021093-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520666 P-0021093-T01-WES P-0021093-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556774 P-0021094-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021094-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520669 P-0021094-N01-WES P-0021094-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556775 P-0021094-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021094-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520667 P-0021094-T01-WES P-0021094-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556776 P-0021095-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021095-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520668 P-0021095-N01-WES P-0021095-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556777 P-0021095-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021095-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520670 P-0021095-T01-WES P-0021095-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556778 P-0021098-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021098-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520672 P-0021098-N01-WES P-0021098-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556780 P-0021098-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021098-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520673 P-0021098-T01-WES P-0021098-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556781 P-0021099-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021099-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520674 P-0021099-N01-WES P-0021099-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556782 P-0021099-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021099-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520675 P-0021099-T01-WES P-0021099-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556783 P-0021100-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021100-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520677 P-0021100-N01-WES P-0021100-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556784 P-0021100-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021100-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520676 P-0021100-T01-WES P-0021100-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556785 P-0021103-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021103-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520678 P-0021103-N01-WES P-0021103-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556786 P-0021103-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021103-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520679 P-0021103-T01-WES P-0021103-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556787 P-0021104-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021104-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520680 P-0021104-N01-WES P-0021104-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556788 P-0021104-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021104-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520681 P-0021104-T01-WES P-0021104-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556789 P-0021105-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021105-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520682 P-0021105-N01-WES P-0021105-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556790 P-0021105-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021105-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520683 P-0021105-T01-WES P-0021105-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556791 P-0021106-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021106-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520685 P-0021106-N01-WES P-0021106-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556792 P-0021106-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021106-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520684 P-0021106-T01-WES P-0021106-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556793 P-0021107-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021107-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520686 P-0021107-N01-WES P-0021107-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556794 P-0021107-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021107-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520688 P-0021107-T01-WES P-0021107-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556795 P-0019905-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019905-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520687 P-0019905-N01-WES P-0019905-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556796 P-0019905-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019905-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520690 P-0019905-T02-WES P-0019905-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556797 P-0019909-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019909-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520689 P-0019909-N01-WES P-0019909-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556798 P-0019909-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019909-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520691 P-0019909-T02-WES P-0019909-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556800 P-0019930-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019930-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520692 P-0019930-N01-WES P-0019930-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556801 P-0019930-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019930-T01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520694 P-0019930-T01-WES P-0019930-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556802 P-0019933-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019933-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520697 P-0019933-N01-WES P-0019933-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556803 P-0019933-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019933-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520695 P-0019933-T01-WES P-0019933-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556804 P-0019975-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019975-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520696 P-0019975-N01-WES P-0019975-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556805 P-0019975-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019975-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520698 P-0019975-T01-WES P-0019975-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556806 P-0019988-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0019988-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520699 P-0019988-N01-WES P-0019988-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556807 P-0019988-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0019988-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520700 P-0019988-T02-WES P-0019988-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556808 P-0020063-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020063-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520701 P-0020063-N01-WES P-0020063-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556809 P-0020063-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020063-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520702 P-0020063-T01-WES P-0020063-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556810 P-0020076-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020076-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520703 P-0020076-N01-WES P-0020076-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556811 P-0020076-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020076-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520704 P-0020076-T02-WES P-0020076-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556812 P-0020086-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020086-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520705 P-0020086-N01-WES P-0020086-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556814 P-0020086-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020086-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520707 P-0020086-T01-WES P-0020086-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556815 P-0020161-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020161-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520709 P-0020161-N01-WES P-0020161-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556816 P-0020161-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020161-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520708 P-0020161-T01-WES P-0020161-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556817 P-0020197-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020197-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520710 P-0020197-N01-WES P-0020197-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556818 P-0020197-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020197-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520711 P-0020197-T02-WES P-0020197-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556819 P-0020283-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020283-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520713 P-0020283-N01-WES P-0020283-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556820 P-0020283-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020283-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520712 P-0020283-T02-WES P-0020283-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556821 P-0021109-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021109-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520714 P-0021109-N01-WES P-0021109-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556822 P-0021109-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021109-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520715 P-0021109-T01-WES P-0021109-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556823 P-0021110-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021110-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520716 P-0021110-N01-WES P-0021110-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556824 P-0021110-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021110-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520718 P-0021110-T01-WES P-0021110-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556825 P-0021111-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021111-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520717 P-0021111-N01-WES P-0021111-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556826 P-0021111-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021111-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520719 P-0021111-T01-WES P-0021111-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556827 P-0021112-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021112-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520720 P-0021112-N01-WES P-0021112-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556828 P-0021112-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021112-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520721 P-0021112-T01-WES P-0021112-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556829 P-0021114-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021114-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520722 P-0021114-N01-WES P-0021114-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556830 P-0021114-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021114-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520723 P-0021114-T01-WES P-0021114-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556831 P-0021115-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021115-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520724 P-0021115-N01-WES P-0021115-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556832 P-0021115-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021115-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520725 P-0021115-T01-WES P-0021115-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556834 P-0021116-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021116-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520726 P-0021116-N01-WES P-0021116-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556835 P-0021116-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021116-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520728 P-0021116-T01-WES P-0021116-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556836 P-0021117-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021117-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520729 P-0021117-N01-WES P-0021117-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556837 P-0021117-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021117-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520730 P-0021117-T01-WES P-0021117-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556838 P-0021119-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021119-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520731 P-0021119-N01-WES P-0021119-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556839 P-0021119-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021119-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520732 P-0021119-T01-WES P-0021119-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556840 P-0021122-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021122-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520734 P-0021122-N01-WES P-0021122-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556841 P-0021122-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021122-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520733 P-0021122-T01-WES P-0021122-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556842 P-0021123-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021123-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520735 P-0021123-N01-WES P-0021123-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556843 P-0021123-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021123-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520737 P-0021123-T01-WES P-0021123-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556844 P-0021125-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021125-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520736 P-0021125-N01-WES P-0021125-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556845 P-0021125-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021125-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520738 P-0021125-T01-WES P-0021125-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556846 P-0020295-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020295-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520739 P-0020295-N01-WES P-0020295-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556847 P-0020295-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020295-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520740 P-0020295-T01-WES P-0020295-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556848 P-0020309-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020309-N01 SRP189097 phs001783 "Paired-end sequencing was carried out on Illumina HiSeq 2500,Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit." SRS4520741 P-0020309-N01-WES P-0020309-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 2500 alignment_software BWA MEM SRX5556849 P-0020309-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020309-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520742 P-0020309-T01-WES P-0020309-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556850 P-0020313-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020313-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520743 P-0020313-N01-WES P-0020313-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556851 P-0020313-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020313-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with SureSelectXT Human All Exon V4 kit. SRS4520744 P-0020313-T01-WES P-0020313-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556852 P-0020367-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020367-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520745 P-0020367-N01-WES P-0020367-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556853 P-0020367-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020367-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520746 P-0020367-T02-WES P-0020367-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556854 P-0020399-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020399-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520747 P-0020399-N01-WES P-0020399-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556855 P-0020399-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020399-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520748 P-0020399-T01-WES P-0020399-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556856 P-0020437-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020437-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520749 P-0020437-N01-WES P-0020437-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556857 P-0020437-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020437-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520750 P-0020437-T02-WES P-0020437-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556858 P-0020482-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020482-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520751 P-0020482-N01-WES P-0020482-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556859 P-0020482-T02-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020482-T02 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520754 P-0020482-T02-WES P-0020482-T02-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556860 P-0020540-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020540-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520752 P-0020540-N01-WES P-0020540-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556861 P-0020540-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020540-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520753 P-0020540-T01-WES P-0020540-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556862 P-0020541-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020541-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520755 P-0020541-N01-WES P-0020541-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556863 P-0020541-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020541-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520756 P-0020541-T01-WES P-0020541-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556864 P-0020542-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020542-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520757 P-0020542-N01-WES P-0020542-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556865 P-0020542-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020542-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520758 P-0020542-T01-WES P-0020542-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556866 P-0020544-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020544-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520759 P-0020544-N01-WES P-0020544-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556867 P-0020544-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020544-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520760 P-0020544-T01-WES P-0020544-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556868 P-0020545-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0020545-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520761 P-0020545-N01-WES P-0020545-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556869 P-0020545-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0020545-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520762 P-0020545-T01-WES P-0020545-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556870 P-0021126-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021126-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520763 P-0021126-N01-WES P-0021126-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556871 P-0021126-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021126-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520764 P-0021126-T01-WES P-0021126-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556872 P-0021128-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021128-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520765 P-0021128-N01-WES P-0021128-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556873 P-0021128-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021128-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520767 P-0021128-T01-WES P-0021128-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556874 P-0021148-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021148-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520766 P-0021148-N01-WES P-0021148-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556875 P-0021148-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021148-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520768 P-0021148-T01-WES P-0021148-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556876 P-0021149-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021149-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520769 P-0021149-N01-WES P-0021149-N01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556877 P-0021149-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021149-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina HiSeq 4000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520770 P-0021149-T01-WES P-0021149-T01-WES WXS GENOMIC Hybrid Selection 250 0 Application Read Forward 1 1 Application Read Reverse 126 Illumina HiSeq 4000 alignment_software BWA MEM SRX5556878 P-0021150-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021150-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520771 P-0021150-N01-WES P-0021150-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556879 P-0021150-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021150-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520772 P-0021150-T01-WES P-0021150-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556880 P-0021151-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021151-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520773 P-0021151-N01-WES P-0021151-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556881 P-0021151-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021151-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520774 P-0021151-T01-WES P-0021151-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556882 P-0021152-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021152-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520775 P-0021152-N01-WES P-0021152-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556883 P-0021152-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021152-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520776 P-0021152-T01-WES P-0021152-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556884 P-0021153-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021153-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520777 P-0021153-N01-WES P-0021153-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556885 P-0021153-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021153-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520778 P-0021153-T01-WES P-0021153-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556886 P-0021154-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021154-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520779 P-0021154-N01-WES P-0021154-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556887 P-0021154-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021154-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520780 P-0021154-T01-WES P-0021154-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556888 P-0021155-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021155-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520781 P-0021155-N01-WES P-0021155-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556889 P-0021155-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021155-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520782 P-0021155-T01-WES P-0021155-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556890 P-0021156-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021156-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520783 P-0021156-N01-WES P-0021156-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556891 P-0021156-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021156-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520784 P-0021156-T01-WES P-0021156-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556892 P-0021158-N01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from normal blood sample P-0021158-N01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520785 P-0021158-N01-WES P-0021158-N01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM SRX5556893 P-0021158-T01-WES Exome sequencing of recaptured genomic library from MSK-IMPACT from clinical tumor specimen P-0021158-T01 SRP189097 phs001783 Paired-end sequencing was carried out on Illumina NovaSeq 6000 after target capture with xGen Exome Research Panel v1.0 kit. SRS4520786 P-0021158-T01-WES P-0021158-T01-WES WXS GENOMIC Hybrid Selection 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina NovaSeq 6000 alignment_software BWA MEM