SRX19889436 CCSORC001793-1001-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243463 1001-V1 CCSORC001793-1001-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889437 CCSORC001793-1001-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243464 1001-V1_4-6 CCSORC001793-1001-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889438 CCSORC001793-1003-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243465 1003-V1 CCSORC001793-1003-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889439 CCSORC001793-1040-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243466 1040-V1_4-6 CCSORC001793-1040-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889440 CCSORC001793-1040-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243467 1040-V2 CCSORC001793-1040-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889441 CCSORC001793-1040-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243468 1040-V3 CCSORC001793-1040-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889442 CCSORC001793-1004-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243469 1004-V1_4-6 CCSORC001793-1004-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889443 CCSORC001793-1040-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243470 1040-V4 CCSORC001793-1040-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889444 CCSORC001793-1041-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243471 1041-V1 CCSORC001793-1041-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889445 CCSORC001793-1041-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243472 1041-V1_4-6 CCSORC001793-1041-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889446 CCSORC001793-1041-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243473 1041-V2 CCSORC001793-1041-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889447 CCSORC001793-1041-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243474 1041-V3 CCSORC001793-1041-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889448 CCSORC001793-1041-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243475 1041-V4 CCSORC001793-1041-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889449 CCSORC001793-1042-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243476 1042-V1 CCSORC001793-1042-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889450 CCSORC001793-1042-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243477 1042-V1_4-6 CCSORC001793-1042-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889451 CCSORC001793-1042-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243478 1042-V2 CCSORC001793-1042-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889452 CCSORC001793-1042-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243479 1042-V3 CCSORC001793-1042-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889453 CCSORC001793-1004-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243480 1004-V2 CCSORC001793-1004-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889454 CCSORC001793-1042-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243481 1042-V4 CCSORC001793-1042-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889455 CCSORC001793-1043-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243482 1043-V1 CCSORC001793-1043-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889456 CCSORC001793-1043-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243483 1043-V1_4-6 CCSORC001793-1043-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889457 CCSORC001793-1043-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243484 1043-V2 CCSORC001793-1043-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889458 CCSORC001793-1043-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243485 1043-V3 CCSORC001793-1043-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889459 CCSORC001793-1043-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243486 1043-V4 CCSORC001793-1043-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889460 CCSORC001793-1049-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243487 1049-V1_4-6 CCSORC001793-1049-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889461 CCSORC001793-1049-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243488 1049-V2 CCSORC001793-1049-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889462 CCSORC001793-1049-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243489 1049-V3 CCSORC001793-1049-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889463 CCSORC001793-1049-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243490 1049-V4 CCSORC001793-1049-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889464 CCSORC001793-1050-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243491 1050-V1 CCSORC001793-1050-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889465 CCSORC001793-1001-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243492 1001-V2 CCSORC001793-1001-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889466 CCSORC001793-1005-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243493 1005-V1 CCSORC001793-1005-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889467 CCSORC001793-1050-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243494 1050-V1_4-6 CCSORC001793-1050-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889468 CCSORC001793-1050-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243495 1050-V2 CCSORC001793-1050-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889469 CCSORC001793-1050-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243496 1050-V3 CCSORC001793-1050-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889470 CCSORC001793-1050-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243497 1050-V4 CCSORC001793-1050-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889471 CCSORC001793-1051-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243498 1051-V1 CCSORC001793-1051-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889472 CCSORC001793-1051-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243499 1051-V1_4-6 CCSORC001793-1051-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889473 CCSORC001793-1051-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243500 1051-V2 CCSORC001793-1051-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889474 CCSORC001793-1051-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243501 1051-V3 CCSORC001793-1051-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889475 CCSORC001793-1051-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243502 1051-V4 CCSORC001793-1051-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889476 CCSORC001793-1052-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243503 1052-V1 CCSORC001793-1052-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889477 CCSORC001793-1005-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243504 1005-V1_4-6 CCSORC001793-1005-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889478 CCSORC001793-1052-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243505 1052-V1_4-6 CCSORC001793-1052-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889479 CCSORC001793-1052-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243506 1052-V3 CCSORC001793-1052-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889480 CCSORC001793-1052-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243507 1052-V2 CCSORC001793-1052-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889481 CCSORC001793-1086-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243509 1086-V4 CCSORC001793-1086-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889482 CCSORC001793-1087-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243508 1087-V1 CCSORC001793-1087-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889483 CCSORC001793-1008-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243510 1008-V2 CCSORC001793-1008-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889484 CCSORC001793-1087-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243511 1087-V1_4-6 CCSORC001793-1087-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889485 CCSORC001793-1087-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243512 1087-V2 CCSORC001793-1087-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889486 CCSORC001793-1087-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243513 1087-V3 CCSORC001793-1087-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889487 CCSORC001793-1087-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243514 1087-V4 CCSORC001793-1087-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889488 CCSORC001793-1088-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243515 1088-V1 CCSORC001793-1088-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889489 CCSORC001793-1088-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243516 1088-V1_4-6 CCSORC001793-1088-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889490 CCSORC001793-1088-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243517 1088-V2 CCSORC001793-1088-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889491 CCSORC001793-1088-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243518 1088-V3 CCSORC001793-1088-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889492 CCSORC001793-1088-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243519 1088-V4 CCSORC001793-1088-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889493 CCSORC001793-1089-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243520 1089-V1 CCSORC001793-1089-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889494 CCSORC001793-1009-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243521 1009-V1 CCSORC001793-1009-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889495 CCSORC001793-1089-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243522 1089-V1_4-6 CCSORC001793-1089-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889496 CCSORC001793-1089-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243523 1089-V2 CCSORC001793-1089-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889497 CCSORC001793-1089-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243524 1089-V3 CCSORC001793-1089-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889498 CCSORC001793-1089-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243525 1089-V4 CCSORC001793-1089-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889499 CCSORC001793-1090-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243526 1090-V1 CCSORC001793-1090-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889500 CCSORC001793-1090-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243528 1090-V1_4-6 CCSORC001793-1090-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889501 CCSORC001793-1090-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243527 1090-V2 CCSORC001793-1090-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889502 CCSORC001793-1099-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243529 1099-V1_4-6 CCSORC001793-1099-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889503 CCSORC001793-1099-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243530 1099-V2 CCSORC001793-1099-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889504 CCSORC001793-1099-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243531 1099-V3 CCSORC001793-1099-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889505 CCSORC001793-1099-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243532 1099-V4 CCSORC001793-1099-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889506 CCSORC001793-1100-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243534 1100-V1 CCSORC001793-1100-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889507 CCSORC001793-1010-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243533 1010-V1 CCSORC001793-1010-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889508 CCSORC001793-1100-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243535 1100-V1_4-6 CCSORC001793-1100-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889509 CCSORC001793-1100-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243536 1100-V2 CCSORC001793-1100-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889510 CCSORC001793-1100-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243537 1100-V3 CCSORC001793-1100-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889511 CCSORC001793-1100-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243538 1100-V4 CCSORC001793-1100-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889512 CCSORC001793-1101-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243539 1101-V1 CCSORC001793-1101-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889513 CCSORC001793-1101-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243540 1101-V1_4-6 CCSORC001793-1101-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889514 CCSORC001793-1101-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243541 1101-V2 CCSORC001793-1101-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889515 CCSORC001793-1101-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243542 1101-V3 CCSORC001793-1101-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889516 CCSORC001793-1101-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243543 1101-V4 CCSORC001793-1101-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889517 CCSORC001793-1102-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243544 1102-V1 CCSORC001793-1102-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889518 CCSORC001793-1010-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243545 1010-V1_4-6 CCSORC001793-1010-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889519 CCSORC001793-1102-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243546 1102-V1_4-6 CCSORC001793-1102-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889520 CCSORC001793-1102-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243547 1102-V2 CCSORC001793-1102-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889521 CCSORC001793-1102-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243548 1102-V3 CCSORC001793-1102-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889522 CCSORC001793-1102-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243549 1102-V4 CCSORC001793-1102-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889523 CCSORC001793-1103-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243550 1103-V1 CCSORC001793-1103-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889524 CCSORC001793-1103-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243551 1103-V1_4-6 CCSORC001793-1103-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889525 CCSORC001793-1103-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243552 1103-V2 CCSORC001793-1103-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889526 CCSORC001793-1103-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243553 1103-V3 CCSORC001793-1103-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889527 CCSORC001793-1103-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243554 1103-V4 CCSORC001793-1103-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889528 CCSORC001793-1104-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243555 1104-V1 CCSORC001793-1104-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889529 CCSORC001793-1010-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243556 1010-V2 CCSORC001793-1010-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889530 CCSORC001793-1104-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243557 1104-V1_4-6 CCSORC001793-1104-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889531 CCSORC001793-1104-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243558 1104-V3 CCSORC001793-1104-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889532 CCSORC001793-1105-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243560 1105-V1 CCSORC001793-1105-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889533 CCSORC001793-1105-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243559 1105-V1_4-6 CCSORC001793-1105-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889534 CCSORC001793-1105-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243561 1105-V2 CCSORC001793-1105-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889535 CCSORC001793-1105-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243562 1105-V3 CCSORC001793-1105-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889536 CCSORC001793-1105-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243563 1105-V4 CCSORC001793-1105-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889537 CCSORC001793-1106-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243564 1106-V1 CCSORC001793-1106-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889538 CCSORC001793-1106-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243565 1106-V1_4-6 CCSORC001793-1106-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889539 CCSORC001793-1106-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243566 1106-V2 CCSORC001793-1106-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889540 CCSORC001793-1010-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243567 1010-V3 CCSORC001793-1010-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889541 CCSORC001793-1106-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243568 1106-V3 CCSORC001793-1106-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889542 CCSORC001793-1106-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243569 1106-V4 CCSORC001793-1106-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889543 CCSORC001793-1107-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243570 1107-V1 CCSORC001793-1107-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889544 CCSORC001793-1125-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243571 1125-V1 CCSORC001793-1125-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889545 CCSORC001793-1125-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243572 1125-V1_4-6 CCSORC001793-1125-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889546 CCSORC001793-1125-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243574 1125-V2 CCSORC001793-1125-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889547 CCSORC001793-1125-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243573 1125-V3 CCSORC001793-1125-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889548 CCSORC001793-1125-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243575 1125-V4 CCSORC001793-1125-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889549 CCSORC001793-1126-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243576 1126-V1_4-6 CCSORC001793-1126-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889550 CCSORC001793-1126-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243577 1126-V2 CCSORC001793-1126-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889551 CCSORC001793-1126-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243578 1126-V3 CCSORC001793-1126-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889552 CCSORC001793-1126-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243579 1126-V4 CCSORC001793-1126-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889553 CCSORC001793-1128-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243580 1128-V1 CCSORC001793-1128-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889554 CCSORC001793-1012-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243581 1012-V2 CCSORC001793-1012-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889555 CCSORC001793-1128-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243582 1128-V1_4-6 CCSORC001793-1128-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889556 CCSORC001793-1128-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243583 1128-V2 CCSORC001793-1128-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889557 CCSORC001793-1128-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243584 1128-V3 CCSORC001793-1128-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889558 CCSORC001793-1128-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243585 1128-V4 CCSORC001793-1128-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889559 CCSORC001793-1129-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243587 1129-V1 CCSORC001793-1129-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889560 CCSORC001793-1129-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243586 1129-V1_4-6 CCSORC001793-1129-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889561 CCSORC001793-1129-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243588 1129-V2 CCSORC001793-1129-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889562 CCSORC001793-1129-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243589 1129-V3 CCSORC001793-1129-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889563 CCSORC001793-1129-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243590 1129-V4 CCSORC001793-1129-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889564 CCSORC001793-1130-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243591 1130-V1 CCSORC001793-1130-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889565 CCSORC001793-1134-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243592 1134-V1_4-6 CCSORC001793-1134-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889566 CCSORC001793-1013-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243593 1013-V1 CCSORC001793-1013-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889567 CCSORC001793-1134-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243594 1134-V2 CCSORC001793-1134-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889568 CCSORC001793-1134-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243595 1134-V3 CCSORC001793-1134-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889569 CCSORC001793-1134-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243597 1134-V4 CCSORC001793-1134-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889570 CCSORC001793-1135-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243596 1135-V1 CCSORC001793-1135-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889571 CCSORC001793-1135-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243598 1135-V1_4-6 CCSORC001793-1135-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889572 CCSORC001793-1135-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243599 1135-V2 CCSORC001793-1135-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889573 CCSORC001793-1135-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243600 1135-V3 CCSORC001793-1135-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889574 CCSORC001793-1135-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243601 1135-V4 CCSORC001793-1135-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889575 CCSORC001793-1136-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243602 1136-V1 CCSORC001793-1136-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889576 CCSORC001793-1136-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243603 1136-V1_4-6 CCSORC001793-1136-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889577 CCSORC001793-1013-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243604 1013-V1_4-6 CCSORC001793-1013-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889578 CCSORC001793-1136-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243605 1136-V2 CCSORC001793-1136-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889579 CCSORC001793-1136-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243606 1136-V3 CCSORC001793-1136-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889580 CCSORC001793-1136-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243607 1136-V4 CCSORC001793-1136-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889581 CCSORC001793-1137-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243608 1137-V1 CCSORC001793-1137-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889582 CCSORC001793-1137-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243609 1137-V1_4-6 CCSORC001793-1137-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889583 CCSORC001793-1137-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243610 1137-V2 CCSORC001793-1137-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889584 CCSORC001793-1137-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243611 1137-V3 CCSORC001793-1137-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889585 CCSORC001793-1137-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243612 1137-V4 CCSORC001793-1137-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889586 CCSORC001793-1138-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243614 1138-V1 CCSORC001793-1138-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889587 CCSORC001793-1024-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243613 1024-V2 CCSORC001793-1024-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889588 CCSORC001793-1024-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243615 1024-V3 CCSORC001793-1024-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889589 CCSORC001793-1024-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243616 1024-V4 CCSORC001793-1024-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889590 CCSORC001793-1025-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243617 1025-V1 CCSORC001793-1025-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889591 CCSORC001793-1025-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243618 1025-V1_4-6 CCSORC001793-1025-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889592 CCSORC001793-1025-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243619 1025-V2 CCSORC001793-1025-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889593 CCSORC001793-1025-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243620 1025-V3 CCSORC001793-1025-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889594 CCSORC001793-1025-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243621 1025-V4 CCSORC001793-1025-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889595 CCSORC001793-1027-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243623 1027-V1 CCSORC001793-1027-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889596 CCSORC001793-1027-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243622 1027-V1_4-6 CCSORC001793-1027-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889597 CCSORC001793-1027-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243624 1027-V2 CCSORC001793-1027-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889598 CCSORC001793-1027-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243625 1027-V3 CCSORC001793-1027-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889599 CCSORC001793-1003-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243626 1003-V1_4-6 CCSORC001793-1003-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889600 CCSORC001793-1027-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243627 1027-V4 CCSORC001793-1027-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889601 CCSORC001793-1028-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243628 1028-V1 CCSORC001793-1028-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889602 CCSORC001793-1028-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243629 1028-V1_4-6 CCSORC001793-1028-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889603 CCSORC001793-1028-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243630 1028-V2 CCSORC001793-1028-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889604 CCSORC001793-1028-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243631 1028-V3 CCSORC001793-1028-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889605 CCSORC001793-1028-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243632 1028-V4 CCSORC001793-1028-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889606 CCSORC001793-1030-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243633 1030-V1 CCSORC001793-1030-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889607 CCSORC001793-1030-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243634 1030-V1_4-6 CCSORC001793-1030-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889608 CCSORC001793-1030-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243636 1030-V2 CCSORC001793-1030-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889609 CCSORC001793-1030-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243635 1030-V3 CCSORC001793-1030-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889610 CCSORC001793-1062-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243638 1062-V1_4-6 CCSORC001793-1062-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889611 CCSORC001793-1062-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243637 1062-V2 CCSORC001793-1062-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889612 CCSORC001793-1062-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243639 1062-V3 CCSORC001793-1062-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889613 CCSORC001793-1062-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243640 1062-V4 CCSORC001793-1062-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889614 CCSORC001793-1063-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243641 1063-V1 CCSORC001793-1063-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889615 CCSORC001793-1063-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243642 1063-V1_4-6 CCSORC001793-1063-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889616 CCSORC001793-1063-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243643 1063-V2 CCSORC001793-1063-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889617 CCSORC001793-1063-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243644 1063-V3 CCSORC001793-1063-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889618 CCSORC001793-1006-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243645 1006-V1_4-6 CCSORC001793-1006-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889619 CCSORC001793-1063-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243646 1063-V4 CCSORC001793-1063-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889620 CCSORC001793-1064-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243647 1064-V1 CCSORC001793-1064-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889621 CCSORC001793-1064-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243648 1064-V1_4-6 CCSORC001793-1064-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889622 CCSORC001793-1064-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243649 1064-V2 CCSORC001793-1064-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889623 CCSORC001793-1064-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243650 1064-V3 CCSORC001793-1064-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889624 CCSORC001793-1064-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243651 1064-V4 CCSORC001793-1064-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889625 CCSORC001793-1065-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243653 1065-V1 CCSORC001793-1065-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889626 CCSORC001793-1065-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243652 1065-V1_4-6 CCSORC001793-1065-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889627 CCSORC001793-1065-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243654 1065-V2 CCSORC001793-1065-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889628 CCSORC001793-1065-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243655 1065-V3 CCSORC001793-1065-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889629 CCSORC001793-1006-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243656 1006-V2 CCSORC001793-1006-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889630 CCSORC001793-1065-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243658 1065-V4 CCSORC001793-1065-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889631 CCSORC001793-1079-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243657 1079-V1 CCSORC001793-1079-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889632 CCSORC001793-1007-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243659 1007-V3 CCSORC001793-1007-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889633 CCSORC001793-1079-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243661 1079-V1_4-6 CCSORC001793-1079-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889634 CCSORC001793-1079-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243660 1079-V2 CCSORC001793-1079-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889635 CCSORC001793-1079-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243664 1079-V3 CCSORC001793-1079-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889636 CCSORC001793-1079-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243662 1079-V4 CCSORC001793-1079-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889637 CCSORC001793-1080-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243665 1080-V1 CCSORC001793-1080-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889638 CCSORC001793-1080-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243663 1080-V1_4-6 CCSORC001793-1080-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889639 CCSORC001793-1080-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243666 1080-V2 CCSORC001793-1080-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889640 CCSORC001793-1080-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243668 1080-V3 CCSORC001793-1080-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889641 CCSORC001793-1080-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243667 1080-V4 CCSORC001793-1080-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889642 CCSORC001793-1081-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243669 1081-V1 CCSORC001793-1081-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889643 CCSORC001793-1007-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243671 1007-V4 CCSORC001793-1007-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889644 CCSORC001793-1081-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243672 1081-V1_4-6 CCSORC001793-1081-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889645 CCSORC001793-1081-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243670 1081-V2 CCSORC001793-1081-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889646 CCSORC001793-1081-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243673 1081-V3 CCSORC001793-1081-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889647 CCSORC001793-1081-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243674 1081-V4 CCSORC001793-1081-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889648 CCSORC001793-1082-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243675 1082-V1 CCSORC001793-1082-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889649 CCSORC001793-1082-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243676 1082-V1_4-6 CCSORC001793-1082-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889650 CCSORC001793-1082-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243678 1082-V2 CCSORC001793-1082-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889651 CCSORC001793-1082-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243677 1082-V3 CCSORC001793-1082-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889652 CCSORC001793-1095-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243679 1095-V1_4-6 CCSORC001793-1095-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889653 CCSORC001793-1095-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243680 1095-V2 CCSORC001793-1095-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889654 CCSORC001793-1095-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243681 1095-V3 CCSORC001793-1095-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889655 CCSORC001793-1095-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243684 1095-V4 CCSORC001793-1095-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889656 CCSORC001793-1096-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243682 1096-V1 CCSORC001793-1096-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889657 CCSORC001793-1009-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243683 1009-V3 CCSORC001793-1009-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889658 CCSORC001793-1096-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243685 1096-V1_4-6 CCSORC001793-1096-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889659 CCSORC001793-1096-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243686 1096-V2 CCSORC001793-1096-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889660 CCSORC001793-1096-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243687 1096-V3 CCSORC001793-1096-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889661 CCSORC001793-1096-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243688 1096-V4 CCSORC001793-1096-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889662 CCSORC001793-1097-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243689 1097-V1 CCSORC001793-1097-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889663 CCSORC001793-1097-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243690 1097-V1_4-6 CCSORC001793-1097-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889664 CCSORC001793-1097-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243692 1097-V2 CCSORC001793-1097-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889665 CCSORC001793-1097-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243691 1097-V3 CCSORC001793-1097-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889666 CCSORC001793-1097-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243693 1097-V4 CCSORC001793-1097-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889667 CCSORC001793-1098-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243694 1098-V1 CCSORC001793-1098-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889668 CCSORC001793-1009-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243695 1009-V4 CCSORC001793-1009-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889669 CCSORC001793-1098-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243696 1098-V1_4-6 CCSORC001793-1098-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889670 CCSORC001793-1098-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243697 1098-V2 CCSORC001793-1098-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889671 CCSORC001793-1098-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243698 1098-V3 CCSORC001793-1098-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889672 CCSORC001793-1098-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243699 1098-V4 CCSORC001793-1098-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889673 CCSORC001793-1099-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243700 1099-V1 CCSORC001793-1099-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889674 CCSORC001793-1107-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243701 1107-V1_4-6 CCSORC001793-1107-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889675 CCSORC001793-1107-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243702 1107-V2 CCSORC001793-1107-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889676 CCSORC001793-1107-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243703 1107-V3 CCSORC001793-1107-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889677 CCSORC001793-1107-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243704 1107-V4 CCSORC001793-1107-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889678 CCSORC001793-1109-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243705 1109-V1 CCSORC001793-1109-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889679 CCSORC001793-1109-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243707 1109-V1_4-6 CCSORC001793-1109-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889680 CCSORC001793-1109-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243706 1109-V2 CCSORC001793-1109-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889681 CCSORC001793-1010-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243708 1010-V4 CCSORC001793-1010-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889682 CCSORC001793-1109-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243709 1109-V3 CCSORC001793-1109-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889683 CCSORC001793-1109-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243710 1109-V4 CCSORC001793-1109-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889684 CCSORC001793-1110-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243711 1110-V1 CCSORC001793-1110-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889685 CCSORC001793-1110-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243712 1110-V1_4-6 CCSORC001793-1110-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889686 CCSORC001793-1110-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243713 1110-V2 CCSORC001793-1110-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889687 CCSORC001793-1110-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243714 1110-V3 CCSORC001793-1110-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889688 CCSORC001793-1110-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243715 1110-V4 CCSORC001793-1110-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889689 CCSORC001793-1111-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243716 1111-V1 CCSORC001793-1111-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889690 CCSORC001793-1111-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243717 1111-V1_4-6 CCSORC001793-1111-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889691 CCSORC001793-1111-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243718 1111-V2 CCSORC001793-1111-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889692 CCSORC001793-1011-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243719 1011-V1 CCSORC001793-1011-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889693 CCSORC001793-1111-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243720 1111-V3 CCSORC001793-1111-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889694 CCSORC001793-1111-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243721 1111-V4 CCSORC001793-1111-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889695 CCSORC001793-1112-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243723 1112-V1 CCSORC001793-1112-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889696 CCSORC001793-2017-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243724 2017-V1 CCSORC001793-2017-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889697 CCSORC001793-2018-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243722 2018-V1 CCSORC001793-2018-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889698 CCSORC001793-2019-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243725 2019-V1 CCSORC001793-2019-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889699 CCSORC001793-1013-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243726 1013-V4 CCSORC001793-1013-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889700 CCSORC001793-2020-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243727 2020-V1 CCSORC001793-2020-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889701 CCSORC001793-2021-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243728 2021-V1 CCSORC001793-2021-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889702 CCSORC001793-2022-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243729 2022-V1 CCSORC001793-2022-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889703 CCSORC001793-2024-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243730 2024-V1 CCSORC001793-2024-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889704 CCSORC001793-2027-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243731 2027-V1 CCSORC001793-2027-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889705 CCSORC001793-2028-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243732 2028-V1 CCSORC001793-2028-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889706 CCSORC001793-2029-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243733 2029-V1 CCSORC001793-2029-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889707 CCSORC001793-2031-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243734 2031-V1 CCSORC001793-2031-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889708 CCSORC001793-2032-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243735 2032-V1 CCSORC001793-2032-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889709 CCSORC001793-2033-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243736 2033-V1 CCSORC001793-2033-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889710 CCSORC001793-1015-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243737 1015-V1 CCSORC001793-1015-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889711 CCSORC001793-2034-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243738 2034-V1 CCSORC001793-2034-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889712 CCSORC001793-2035-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243739 2035-V1 CCSORC001793-2035-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889713 CCSORC001793-2036-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243740 2036-V1 CCSORC001793-2036-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889714 CCSORC001793-2037-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243741 2037-V1 CCSORC001793-2037-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889715 CCSORC001793-1023_V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243742 1023_V1_4-6 CCSORC001793-1023_V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889716 CCSORC001793-1023-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243743 1023-V1 CCSORC001793-1023-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889717 CCSORC001793-1045_V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243744 1045_V1_4-6 CCSORC001793-1045_V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889718 CCSORC001793-1020-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243745 1020-V1_4-6 CCSORC001793-1020-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889719 CCSORC001793-1002-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243746 1002-V3 CCSORC001793-1002-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889720 CCSORC001793-1020-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243747 1020-V2 CCSORC001793-1020-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889721 CCSORC001793-1020-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243748 1020-V3 CCSORC001793-1020-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889722 CCSORC001793-1020-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243749 1020-V4 CCSORC001793-1020-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889723 CCSORC001793-1021-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243750 1021-V1 CCSORC001793-1021-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889724 CCSORC001793-1021-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243751 1021-V1_4-6 CCSORC001793-1021-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889725 CCSORC001793-1021-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243752 1021-V2 CCSORC001793-1021-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889726 CCSORC001793-1021-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243753 1021-V3 CCSORC001793-1021-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889727 CCSORC001793-1021-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243754 1021-V4 CCSORC001793-1021-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889728 CCSORC001793-1022-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243755 1022-V1 CCSORC001793-1022-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889729 CCSORC001793-1022-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243758 1022-V1_4-6 CCSORC001793-1022-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889730 CCSORC001793-1002-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243756 1002-V4 CCSORC001793-1002-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889731 CCSORC001793-1022-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243757 1022-V2 CCSORC001793-1022-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889732 CCSORC001793-1022-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243759 1022-V3 CCSORC001793-1022-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889733 CCSORC001793-1022-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243760 1022-V4 CCSORC001793-1022-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889734 CCSORC001793-1023-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243761 1023-V2 CCSORC001793-1023-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889735 CCSORC001793-1023-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243762 1023-V3 CCSORC001793-1023-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889736 CCSORC001793-1023-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243763 1023-V4 CCSORC001793-1023-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889737 CCSORC001793-1024-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243764 1024-V1 CCSORC001793-1024-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889738 CCSORC001793-1024-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243765 1024-V1_4-6 CCSORC001793-1024-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889739 CCSORC001793-1112-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243766 1112-V1_4-6 CCSORC001793-1112-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889740 CCSORC001793-1112-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243767 1112-V2 CCSORC001793-1112-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889741 CCSORC001793-1112-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243768 1112-V3 CCSORC001793-1112-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889742 CCSORC001793-1112-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243769 1112-V4 CCSORC001793-1112-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889743 CCSORC001793-1113-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243770 1113-V1 CCSORC001793-1113-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889744 CCSORC001793-1113-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243771 1113-V1_4-6 CCSORC001793-1113-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889745 CCSORC001793-1113-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243772 1113-V2 CCSORC001793-1113-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889746 CCSORC001793-1011-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243773 1011-V1_4-6 CCSORC001793-1011-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889747 CCSORC001793-1114-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243774 1114-V1 CCSORC001793-1114-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889748 CCSORC001793-1114-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243775 1114-V1_4-6 CCSORC001793-1114-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889749 CCSORC001793-1114-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243776 1114-V2 CCSORC001793-1114-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889750 CCSORC001793-1114-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243777 1114-V3 CCSORC001793-1114-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889751 CCSORC001793-1114-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243778 1114-V4 CCSORC001793-1114-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889752 CCSORC001793-1115-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243779 1115-V1 CCSORC001793-1115-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889753 CCSORC001793-1115-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243780 1115-V1_4-6 CCSORC001793-1115-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889754 CCSORC001793-1115-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243781 1115-V2 CCSORC001793-1115-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889755 CCSORC001793-1115-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243783 1115-V3 CCSORC001793-1115-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889756 CCSORC001793-1115-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243782 1115-V4 CCSORC001793-1115-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889757 CCSORC001793-1002-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243784 1002-V1 CCSORC001793-1002-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889758 CCSORC001793-1011-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243785 1011-V2 CCSORC001793-1011-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889759 CCSORC001793-1117-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243787 1117-V1 CCSORC001793-1117-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889760 CCSORC001793-1121-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243786 1121-V1 CCSORC001793-1121-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889761 CCSORC001793-1121-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243788 1121-V1_4-6 CCSORC001793-1121-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889762 CCSORC001793-1121-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243789 1121-V2 CCSORC001793-1121-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889763 CCSORC001793-1121-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243790 1121-V3 CCSORC001793-1121-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889764 CCSORC001793-1121-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243791 1121-V4 CCSORC001793-1121-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889765 CCSORC001793-1122-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243792 1122-V1 CCSORC001793-1122-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889766 CCSORC001793-1122-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243793 1122-V1_4-6 CCSORC001793-1122-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889767 CCSORC001793-1122-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243795 1122-V2 CCSORC001793-1122-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889768 CCSORC001793-1122-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243794 1122-V3 CCSORC001793-1122-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889769 CCSORC001793-1122-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243796 1122-V4 CCSORC001793-1122-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889770 CCSORC001793-1012-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243797 1012-V1 CCSORC001793-1012-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889771 CCSORC001793-1123-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243799 1123-V1 CCSORC001793-1123-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889772 CCSORC001793-1123-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243798 1123-V1_4-6 CCSORC001793-1123-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889773 CCSORC001793-1123-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243800 1123-V2 CCSORC001793-1123-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889774 CCSORC001793-1123-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243801 1123-V3 CCSORC001793-1123-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889775 CCSORC001793-1123-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243802 1123-V4 CCSORC001793-1123-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889776 CCSORC001793-1124-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243803 1124-V1 CCSORC001793-1124-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889777 CCSORC001793-1124-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243804 1124-V1_4-6 CCSORC001793-1124-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889778 CCSORC001793-1124-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243806 1124-V2 CCSORC001793-1124-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889779 CCSORC001793-1124-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243805 1124-V3 CCSORC001793-1124-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889780 CCSORC001793-1124-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243807 1124-V4 CCSORC001793-1124-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889781 CCSORC001793-1012-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243808 1012-V1_4-6 CCSORC001793-1012-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889782 CCSORC001793-1003-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243809 1003-V2 CCSORC001793-1003-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889783 CCSORC001793-1030-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243810 1030-V4 CCSORC001793-1030-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889784 CCSORC001793-1031-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243811 1031-V1 CCSORC001793-1031-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889785 CCSORC001793-1031-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243813 1031-V1_4-6 CCSORC001793-1031-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889786 CCSORC001793-1031-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243812 1031-V2 CCSORC001793-1031-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889787 CCSORC001793-1031-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243814 1031-V3 CCSORC001793-1031-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889788 CCSORC001793-1031-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243815 1031-V4 CCSORC001793-1031-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889789 CCSORC001793-1034-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243816 1034-V1 CCSORC001793-1034-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889790 CCSORC001793-1034-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243818 1034-V1_4-6 CCSORC001793-1034-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889791 CCSORC001793-1034-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243817 1034-V2 CCSORC001793-1034-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889792 CCSORC001793-1034-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243819 1034-V3 CCSORC001793-1034-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889793 CCSORC001793-1003-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243820 1003-V3 CCSORC001793-1003-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889794 CCSORC001793-1034-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243821 1034-V4 CCSORC001793-1034-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889795 CCSORC001793-1035-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243822 1035-V1 CCSORC001793-1035-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889796 CCSORC001793-1035-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243823 1035-V1_4-6 CCSORC001793-1035-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889797 CCSORC001793-1035-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243824 1035-V2 CCSORC001793-1035-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889798 CCSORC001793-1035-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243825 1035-V3 CCSORC001793-1035-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889799 CCSORC001793-1035-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243826 1035-V4 CCSORC001793-1035-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889800 CCSORC001793-1036-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243827 1036-V1 CCSORC001793-1036-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889801 CCSORC001793-1036-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243828 1036-V1_4-6 CCSORC001793-1036-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889802 CCSORC001793-1052-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243829 1052-V4 CCSORC001793-1052-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889803 CCSORC001793-1053-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243830 1053-V1 CCSORC001793-1053-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889804 CCSORC001793-1053-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243831 1053-V1_4-6 CCSORC001793-1053-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889805 CCSORC001793-1053-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243833 1053-V2 CCSORC001793-1053-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889806 CCSORC001793-1053-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243832 1053-V3 CCSORC001793-1053-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889807 CCSORC001793-1053-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243834 1053-V4 CCSORC001793-1053-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889808 CCSORC001793-1054-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243835 1054-V1 CCSORC001793-1054-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889809 CCSORC001793-1005-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243836 1005-V2 CCSORC001793-1005-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889810 CCSORC001793-1054-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243837 1054-V1_4-6 CCSORC001793-1054-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889811 CCSORC001793-1054-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243838 1054-V2 CCSORC001793-1054-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889812 CCSORC001793-1054-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243839 1054-V3 CCSORC001793-1054-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889813 CCSORC001793-1054-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243841 1054-V4 CCSORC001793-1054-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889814 CCSORC001793-1055-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243840 1055-V1 CCSORC001793-1055-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889815 CCSORC001793-1055-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243842 1055-V1_4-6 CCSORC001793-1055-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889816 CCSORC001793-1055-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243843 1055-V2 CCSORC001793-1055-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889817 CCSORC001793-1055-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243844 1055-V3 CCSORC001793-1055-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889818 CCSORC001793-1055-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243845 1055-V4 CCSORC001793-1055-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889819 CCSORC001793-1056-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243846 1056-V1 CCSORC001793-1056-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889820 CCSORC001793-1005-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243847 1005-V3 CCSORC001793-1005-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889821 CCSORC001793-1056-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243848 1056-V1_4-6 CCSORC001793-1056-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889822 CCSORC001793-1056-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243849 1056-V2 CCSORC001793-1056-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889823 CCSORC001793-1056-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243850 1056-V3 CCSORC001793-1056-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889824 CCSORC001793-1066-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243852 1066-V1 CCSORC001793-1066-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889825 CCSORC001793-1066-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243851 1066-V1_4-6 CCSORC001793-1066-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889826 CCSORC001793-1066-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243853 1066-V2 CCSORC001793-1066-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889827 CCSORC001793-1066-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243854 1066-V3 CCSORC001793-1066-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889828 CCSORC001793-1066-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243855 1066-V4 CCSORC001793-1066-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889829 CCSORC001793-1067-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243856 1067-V1 CCSORC001793-1067-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889830 CCSORC001793-1067-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243857 1067-V1_4-6 CCSORC001793-1067-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889831 CCSORC001793-1067-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243858 1067-V2 CCSORC001793-1067-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889832 CCSORC001793-1067-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243859 1067-V3 CCSORC001793-1067-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889833 CCSORC001793-1006-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243860 1006-V3 CCSORC001793-1006-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889834 CCSORC001793-1067-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243861 1067-V4 CCSORC001793-1067-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889835 CCSORC001793-1068-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243862 1068-V1_4-6 CCSORC001793-1068-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889836 CCSORC001793-1068-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243863 1068-V2 CCSORC001793-1068-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889837 CCSORC001793-1068-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243864 1068-V3 CCSORC001793-1068-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889838 CCSORC001793-1068-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243865 1068-V4 CCSORC001793-1068-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889839 CCSORC001793-1069-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243866 1069-V1 CCSORC001793-1069-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889840 CCSORC001793-1069-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243867 1069-V1_4-6 CCSORC001793-1069-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889841 CCSORC001793-1069-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243868 1069-V2 CCSORC001793-1069-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889842 CCSORC001793-1069-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243869 1069-V3 CCSORC001793-1069-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889843 CCSORC001793-1069-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243870 1069-V4 CCSORC001793-1069-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889844 CCSORC001793-1006-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243871 1006-V4 CCSORC001793-1006-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889845 CCSORC001793-1082-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243872 1082-V4 CCSORC001793-1082-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889846 CCSORC001793-1083-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243873 1083-V1 CCSORC001793-1083-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889847 CCSORC001793-1008-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243874 1008-V1 CCSORC001793-1008-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889848 CCSORC001793-1083-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243875 1083-V1_4-6 CCSORC001793-1083-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889849 CCSORC001793-1083-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243876 1083-V2 CCSORC001793-1083-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889850 CCSORC001793-1083-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243877 1083-V3 CCSORC001793-1083-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889851 CCSORC001793-1083-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243879 1083-V4 CCSORC001793-1083-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889852 CCSORC001793-1084-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243878 1084-V1 CCSORC001793-1084-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889853 CCSORC001793-1084-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243881 1084-V1_4-6 CCSORC001793-1084-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889854 CCSORC001793-1084-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243880 1084-V2 CCSORC001793-1084-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889855 CCSORC001793-1084-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243882 1084-V3 CCSORC001793-1084-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889856 CCSORC001793-1084-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243884 1084-V4 CCSORC001793-1084-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889857 CCSORC001793-1085-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243883 1085-V1 CCSORC001793-1085-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889858 CCSORC001793-1008-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243885 1008-V1_4-6 CCSORC001793-1008-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889859 CCSORC001793-1085-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243886 1085-V1_4-6 CCSORC001793-1085-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889860 CCSORC001793-1085-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243887 1085-V2 CCSORC001793-1085-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889861 CCSORC001793-1085-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243888 1085-V3 CCSORC001793-1085-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889862 CCSORC001793-1085-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243889 1085-V4 CCSORC001793-1085-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889863 CCSORC001793-1086-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243891 1086-V1 CCSORC001793-1086-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889864 CCSORC001793-1086-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243890 1086-V1_4-6 CCSORC001793-1086-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889865 CCSORC001793-1086-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243892 1086-V2 CCSORC001793-1086-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889866 CCSORC001793-1086-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243893 1086-V3 CCSORC001793-1086-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889867 CCSORC001793-1036-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243894 1036-V2 CCSORC001793-1036-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889868 CCSORC001793-1036-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243895 1036-V3 CCSORC001793-1036-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889869 CCSORC001793-1003-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243896 1003-V4 CCSORC001793-1003-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889870 CCSORC001793-1036-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243897 1036-V4 CCSORC001793-1036-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889871 CCSORC001793-1037-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243898 1037-V1 CCSORC001793-1037-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889872 CCSORC001793-1037-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243899 1037-V1_4-6 CCSORC001793-1037-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889873 CCSORC001793-1037-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243900 1037-V2 CCSORC001793-1037-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889874 CCSORC001793-1037-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243901 1037-V3 CCSORC001793-1037-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889875 CCSORC001793-1037-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243902 1037-V4 CCSORC001793-1037-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889876 CCSORC001793-1038-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243904 1038-V1 CCSORC001793-1038-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889877 CCSORC001793-1038-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243903 1038-V1_4-6 CCSORC001793-1038-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889878 CCSORC001793-1038-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243905 1038-V2 CCSORC001793-1038-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889879 CCSORC001793-1038-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243906 1038-V3 CCSORC001793-1038-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889880 CCSORC001793-1004-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243907 1004-V1 CCSORC001793-1004-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889881 CCSORC001793-1038-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243908 1038-V4 CCSORC001793-1038-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889882 CCSORC001793-1039-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243909 1039-V1 CCSORC001793-1039-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889883 CCSORC001793-1039-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243910 1039-V1_4-6 CCSORC001793-1039-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889884 CCSORC001793-1039-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243911 1039-V2 CCSORC001793-1039-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889885 CCSORC001793-1039-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243912 1039-V3 CCSORC001793-1039-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889886 CCSORC001793-1039-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243913 1039-V4 CCSORC001793-1039-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889887 CCSORC001793-1040-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243914 1040-V1 CCSORC001793-1040-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889888 CCSORC001793-1044-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243915 1044-V1 CCSORC001793-1044-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889889 CCSORC001793-1044-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243916 1044-V1_4-6 CCSORC001793-1044-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889890 CCSORC001793-1044-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243917 1044-V2 CCSORC001793-1044-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889891 CCSORC001793-1044-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243918 1044-V3 CCSORC001793-1044-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889892 CCSORC001793-1004-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243919 1004-V3 CCSORC001793-1004-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889893 CCSORC001793-1044-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243921 1044-V4 CCSORC001793-1044-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889894 CCSORC001793-1045-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243920 1045-V2 CCSORC001793-1045-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889895 CCSORC001793-1045-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243924 1045-V3 CCSORC001793-1045-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889896 CCSORC001793-1045-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243922 1045-V4 CCSORC001793-1045-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889897 CCSORC001793-1047-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243923 1047-V1 CCSORC001793-1047-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889898 CCSORC001793-1047-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243925 1047-V1_4-6 CCSORC001793-1047-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889899 CCSORC001793-1047-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243926 1047-V2 CCSORC001793-1047-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889900 CCSORC001793-1047-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243927 1047-V3 CCSORC001793-1047-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889901 CCSORC001793-1047-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243928 1047-V4 CCSORC001793-1047-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889902 CCSORC001793-1048-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243929 1048-V1 CCSORC001793-1048-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889903 CCSORC001793-1004-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243930 1004-V4 CCSORC001793-1004-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889904 CCSORC001793-1048-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243932 1048-V1_4-6 CCSORC001793-1048-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889905 CCSORC001793-1048-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243931 1048-V2 CCSORC001793-1048-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889906 CCSORC001793-1048-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243933 1048-V3 CCSORC001793-1048-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889907 CCSORC001793-1049-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243934 1049-V1 CCSORC001793-1049-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889908 CCSORC001793-1048-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243935 1048-V4 CCSORC001793-1048-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889909 CCSORC001793-1056-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243936 1056-V4 CCSORC001793-1056-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889910 CCSORC001793-1057-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243937 1057-V1 CCSORC001793-1057-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889911 CCSORC001793-1057-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243938 1057-V1_4-6 CCSORC001793-1057-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889912 CCSORC001793-1057-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243939 1057-V2 CCSORC001793-1057-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889913 CCSORC001793-1057-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243940 1057-V3 CCSORC001793-1057-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889914 CCSORC001793-1057-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243941 1057-V4 CCSORC001793-1057-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889915 CCSORC001793-1058-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243942 1058-V1 CCSORC001793-1058-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889916 CCSORC001793-1005-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243943 1005-V4 CCSORC001793-1005-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889917 CCSORC001793-1058-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243944 1058-V1_4-6 CCSORC001793-1058-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889918 CCSORC001793-1058-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243945 1058-V2 CCSORC001793-1058-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889919 CCSORC001793-1058-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243947 1058-V3 CCSORC001793-1058-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889920 CCSORC001793-1058-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243946 1058-V4 CCSORC001793-1058-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889921 CCSORC001793-1059-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243948 1059-V2 CCSORC001793-1059-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889922 CCSORC001793-1059-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243949 1059-V3 CCSORC001793-1059-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889923 CCSORC001793-1059-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243950 1059-V4 CCSORC001793-1059-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889924 CCSORC001793-1061-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243952 1061-V1 CCSORC001793-1061-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889925 CCSORC001793-1061-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243951 1061-V1_4-6 CCSORC001793-1061-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889926 CCSORC001793-1061-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243954 1061-V2 CCSORC001793-1061-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889927 CCSORC001793-1006-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243953 1006-V1 CCSORC001793-1006-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889928 CCSORC001793-1061-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243955 1061-V3 CCSORC001793-1061-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889929 CCSORC001793-1062-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243957 1062-V1 CCSORC001793-1062-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889930 CCSORC001793-1070-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243956 1070-V1_4-6 CCSORC001793-1070-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889931 CCSORC001793-1070-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243958 1070-V2 CCSORC001793-1070-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889932 CCSORC001793-1070-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243959 1070-V3 CCSORC001793-1070-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889933 CCSORC001793-1070-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243960 1070-V4 CCSORC001793-1070-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889934 CCSORC001793-1071-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243961 1071-V1 CCSORC001793-1071-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889935 CCSORC001793-1071-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243962 1071-V1_4-6 CCSORC001793-1071-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889936 CCSORC001793-1071-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243963 1071-V2 CCSORC001793-1071-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889937 CCSORC001793-1071-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243966 1071-V3 CCSORC001793-1071-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889938 CCSORC001793-1071-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243965 1071-V4 CCSORC001793-1071-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889939 CCSORC001793-1072-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243964 1072-V1 CCSORC001793-1072-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889940 CCSORC001793-1001-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243969 1001-V3 CCSORC001793-1001-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889941 CCSORC001793-1007-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243967 1007-V1 CCSORC001793-1007-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889942 CCSORC001793-1072-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243968 1072-V1_4-6 CCSORC001793-1072-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889943 CCSORC001793-1072-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243970 1072-V2 CCSORC001793-1072-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889944 CCSORC001793-1072-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243971 1072-V3 CCSORC001793-1072-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889945 CCSORC001793-1072-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243972 1072-V4 CCSORC001793-1072-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889946 CCSORC001793-1073-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243973 1073-V1 CCSORC001793-1073-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889947 CCSORC001793-1073-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243974 1073-V1_4-6 CCSORC001793-1073-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889948 CCSORC001793-1073-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243975 1073-V2 CCSORC001793-1073-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889949 CCSORC001793-1073-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243976 1073-V3 CCSORC001793-1073-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889950 CCSORC001793-1073-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243978 1073-V4 CCSORC001793-1073-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889951 CCSORC001793-1074-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243979 1074-V1 CCSORC001793-1074-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889952 CCSORC001793-1007-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243977 1007-V1_4-6 CCSORC001793-1007-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889953 CCSORC001793-1074-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243980 1074-V1_4-6 CCSORC001793-1074-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889954 CCSORC001793-1074-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243981 1074-V2 CCSORC001793-1074-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889955 CCSORC001793-1074-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243982 1074-V3 CCSORC001793-1074-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889956 CCSORC001793-1074-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243983 1074-V4 CCSORC001793-1074-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889957 CCSORC001793-1076-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243984 1076-V1 CCSORC001793-1076-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889958 CCSORC001793-1076-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243985 1076-V1_4-6 CCSORC001793-1076-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889959 CCSORC001793-1076-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243986 1076-V2 CCSORC001793-1076-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889960 CCSORC001793-1076-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243988 1076-V3 CCSORC001793-1076-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889961 CCSORC001793-1076-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243987 1076-V4 CCSORC001793-1076-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889962 CCSORC001793-1077-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243989 1077-V1 CCSORC001793-1077-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889963 CCSORC001793-1007-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243990 1007-V2 CCSORC001793-1007-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889964 CCSORC001793-1077-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243991 1077-V1_4-6 CCSORC001793-1077-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889965 CCSORC001793-1077-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243992 1077-V2 CCSORC001793-1077-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889966 CCSORC001793-1077-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243993 1077-V3 CCSORC001793-1077-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889967 CCSORC001793-1077-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243994 1077-V4 CCSORC001793-1077-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889968 CCSORC001793-1078-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243995 1078-V1 CCSORC001793-1078-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889969 CCSORC001793-1078-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243996 1078-V1_4-6 CCSORC001793-1078-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889970 CCSORC001793-1078-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243997 1078-V2 CCSORC001793-1078-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889971 CCSORC001793-1078-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243998 1078-V3 CCSORC001793-1078-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889972 CCSORC001793-1078-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17243999 1078-V4 CCSORC001793-1078-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889973 CCSORC001793-1090-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244001 1090-V3 CCSORC001793-1090-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889974 CCSORC001793-1090-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244000 1090-V4 CCSORC001793-1090-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889975 CCSORC001793-1092-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244002 1092-V1 CCSORC001793-1092-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889976 CCSORC001793-1009-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244003 1009-V1_4-6 CCSORC001793-1009-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889977 CCSORC001793-1092-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244004 1092-V1_4-6 CCSORC001793-1092-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889978 CCSORC001793-1092-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244005 1092-V2 CCSORC001793-1092-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889979 CCSORC001793-1092-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244006 1092-V3 CCSORC001793-1092-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889980 CCSORC001793-1092-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244007 1092-V4 CCSORC001793-1092-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889981 CCSORC001793-1093-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244009 1093-V1 CCSORC001793-1093-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889982 CCSORC001793-1093-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244008 1093-V1_4-6 CCSORC001793-1093-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889983 CCSORC001793-1093-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244010 1093-V2 CCSORC001793-1093-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889984 CCSORC001793-1093-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244011 1093-V3 CCSORC001793-1093-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889985 CCSORC001793-1093-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244012 1093-V4 CCSORC001793-1093-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889986 CCSORC001793-1094-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244014 1094-V1 CCSORC001793-1094-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889987 CCSORC001793-1001-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244013 1001-V4 CCSORC001793-1001-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889988 CCSORC001793-1009-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244015 1009-V2 CCSORC001793-1009-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889989 CCSORC001793-1094-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244016 1094-V1_4-6 CCSORC001793-1094-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889990 CCSORC001793-1094-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244017 1094-V2 CCSORC001793-1094-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889991 CCSORC001793-1094-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244018 1094-V3 CCSORC001793-1094-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889992 CCSORC001793-1094-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244019 1094-V4 CCSORC001793-1094-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889993 CCSORC001793-1095-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244020 1095-V1 CCSORC001793-1095-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889994 CCSORC001793-1117-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244021 1117-V1_4-6 CCSORC001793-1117-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889995 CCSORC001793-1117-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244022 1117-V2 CCSORC001793-1117-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889996 CCSORC001793-1117-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244023 1117-V3 CCSORC001793-1117-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889997 CCSORC001793-1117-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244025 1117-V4 CCSORC001793-1117-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889998 CCSORC001793-1118-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244024 1118-V1 CCSORC001793-1118-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19889999 CCSORC001793-1118-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244026 1118-V1_4-6 CCSORC001793-1118-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890000 CCSORC001793-1118-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244028 1118-V2 CCSORC001793-1118-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890001 CCSORC001793-1118-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244027 1118-V3 CCSORC001793-1118-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890002 CCSORC001793-1118-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244029 1118-V4 CCSORC001793-1118-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890003 CCSORC001793-1011-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244031 1011-V3 CCSORC001793-1011-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890004 CCSORC001793-1119-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244030 1119-V1 CCSORC001793-1119-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890005 CCSORC001793-1119-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244032 1119-V1_4-6 CCSORC001793-1119-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890006 CCSORC001793-1119-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244033 1119-V2 CCSORC001793-1119-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890007 CCSORC001793-1119-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244035 1119-V3 CCSORC001793-1119-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890008 CCSORC001793-1119-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244034 1119-V4 CCSORC001793-1119-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890009 CCSORC001793-1120-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244037 1120-V1 CCSORC001793-1120-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890010 CCSORC001793-1120-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244036 1120-V1_4-6 CCSORC001793-1120-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890011 CCSORC001793-1120-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244038 1120-V2 CCSORC001793-1120-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890012 CCSORC001793-1120-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244039 1120-V3 CCSORC001793-1120-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890013 CCSORC001793-1120-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244040 1120-V4 CCSORC001793-1120-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890014 CCSORC001793-1011-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244041 1011-V4 CCSORC001793-1011-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890015 CCSORC001793-1012-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244042 1012-V3 CCSORC001793-1012-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890016 CCSORC001793-1130-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244044 1130-V1_4-6 CCSORC001793-1130-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890017 CCSORC001793-1130-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244043 1130-V2 CCSORC001793-1130-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890018 CCSORC001793-1130-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244045 1130-V3 CCSORC001793-1130-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890019 CCSORC001793-1130-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244047 1130-V4 CCSORC001793-1130-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890020 CCSORC001793-1131-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244046 1131-V1_4-6 CCSORC001793-1131-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890021 CCSORC001793-1131-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244048 1131-V2 CCSORC001793-1131-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890022 CCSORC001793-1131-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244049 1131-V3 CCSORC001793-1131-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890023 CCSORC001793-1131-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244050 1131-V4 CCSORC001793-1131-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890024 CCSORC001793-1132-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244051 1132-V1 CCSORC001793-1132-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890025 CCSORC001793-1132-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244052 1132-V1_4-6 CCSORC001793-1132-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890026 CCSORC001793-1012-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244055 1012-V4 CCSORC001793-1012-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890027 CCSORC001793-1132-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244053 1132-V2 CCSORC001793-1132-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890028 CCSORC001793-1132-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244054 1132-V3 CCSORC001793-1132-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890029 CCSORC001793-1132-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244056 1132-V4 CCSORC001793-1132-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890030 CCSORC001793-1133-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244058 1133-V1 CCSORC001793-1133-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890031 CCSORC001793-1133-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244057 1133-V1_4-6 CCSORC001793-1133-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890032 CCSORC001793-1133-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244059 1133-V2 CCSORC001793-1133-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890033 CCSORC001793-1133-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244060 1133-V3 CCSORC001793-1133-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890034 CCSORC001793-1133-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244061 1133-V4 CCSORC001793-1133-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890035 CCSORC001793-1134-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244063 1134-V1 CCSORC001793-1134-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890036 CCSORC001793-1138-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244062 1138-V1_4-6 CCSORC001793-1138-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890037 CCSORC001793-1002-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244064 1002-V1_4-6 CCSORC001793-1002-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890038 CCSORC001793-1013-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244065 1013-V2 CCSORC001793-1013-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890039 CCSORC001793-1138-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244066 1138-V2 CCSORC001793-1138-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890040 CCSORC001793-1138-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244067 1138-V3 CCSORC001793-1138-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890041 CCSORC001793-1138-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244068 1138-V4 CCSORC001793-1138-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890042 CCSORC001793-1139-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244069 1139-V1 CCSORC001793-1139-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890043 CCSORC001793-1139-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244070 1139-V1_4-6 CCSORC001793-1139-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890044 CCSORC001793-2001-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244071 2001-V1 CCSORC001793-2001-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890045 CCSORC001793-2002-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244072 2002-V1 CCSORC001793-2002-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890046 CCSORC001793-2003-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244073 2003-V1 CCSORC001793-2003-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890047 CCSORC001793-2004-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244075 2004-V1 CCSORC001793-2004-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890048 CCSORC001793-2005-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244074 2005-V1 CCSORC001793-2005-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890049 CCSORC001793-1013-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244076 1013-V3 CCSORC001793-1013-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890050 CCSORC001793-2006-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244077 2006-V1 CCSORC001793-2006-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890051 CCSORC001793-2008-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244081 2008-V1 CCSORC001793-2008-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890052 CCSORC001793-2010-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244078 2010-V1 CCSORC001793-2010-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890053 CCSORC001793-2011-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244079 2011-V1 CCSORC001793-2011-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890054 CCSORC001793-2013-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244080 2013-V1 CCSORC001793-2013-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890055 CCSORC001793-2015-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244082 2015-V1 CCSORC001793-2015-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890056 CCSORC001793-2016-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244088 2016-V1 CCSORC001793-2016-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890057 CCSORC001793-1045-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244083 1045-V1 CCSORC001793-1045-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890058 CCSORC001793-1059_V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244084 1059_V1_4-6 CCSORC001793-1059_V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890059 CCSORC001793-1059-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244085 1059-V1 CCSORC001793-1059-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890060 CCSORC001793-1015-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244086 1015-V1_4-6 CCSORC001793-1015-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890061 CCSORC001793-2038_V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244087 2038_V1 CCSORC001793-2038_V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890062 CCSORC001793-2039_V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244089 2039_V1 CCSORC001793-2039_V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890063 CCSORC001793-2040_V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244090 2040_V1 CCSORC001793-2040_V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890064 CCSORC001793-1015-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244091 1015-V2 CCSORC001793-1015-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890065 CCSORC001793-1015-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244094 1015-V3 CCSORC001793-1015-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890066 CCSORC001793-1015-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244092 1015-V4 CCSORC001793-1015-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890067 CCSORC001793-1017-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244095 1017-V1 CCSORC001793-1017-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890068 CCSORC001793-1017-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244093 1017-V1_4-6 CCSORC001793-1017-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890069 CCSORC001793-1002-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244096 1002-V2 CCSORC001793-1002-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890070 CCSORC001793-1017-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244097 1017-V2 CCSORC001793-1017-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890071 CCSORC001793-1017-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244098 1017-V3 CCSORC001793-1017-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890072 CCSORC001793-1017-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244099 1017-V4 CCSORC001793-1017-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890073 CCSORC001793-1019-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244100 1019-V1 CCSORC001793-1019-V1 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890074 CCSORC001793-1019-V1_4-6 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244101 1019-V1_4-6 CCSORC001793-1019-V1_4-6 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890075 CCSORC001793-1019-V2 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244102 1019-V2 CCSORC001793-1019-V2 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890076 CCSORC001793-1019-V3 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244103 1019-V3 CCSORC001793-1019-V3 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890077 CCSORC001793-1019-V4 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244104 1019-V4 CCSORC001793-1019-V4 WGS GENOMIC RANDOM Illumina HiSeq X SRX19890078 CCSORC001793-1020-V1 SRP431222 bp0 DNA libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina) and IDT Unique Dual Indexes with total DNA input of 1ng. Genomic DNA was fragmented using a proportional amount of Illumina Nextera XT fragmentation enzyme. Unique dual indexes were added to each sample followed by 12 cycles of PCR to construct libraries. DNA libraries were purified using AMpure magnetic Beads (Beckman Coulter) and eluted in QIAGEN EB buffer. SRS17244105 1020-V1 CCSORC001793-1020-V1 WGS GENOMIC RANDOM Illumina HiSeq X