SRX5336982 WCM10_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using Agilent All Exome V4 (51MB, 4GB seq) SRS4330242 WCM10_1_N_WES_Tumor WCM10_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336983 WCM15_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using Agilent All Exome V4 (51MB, 4GB seq) SRS4330243 WCM15_1_N_WES_Tumor WCM15_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336984 WCM154_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330244 WCM154_1_N_WES_Tumor WCM154_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336985 WCM155_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330245 WCM155_1_N_WES_Tumor WCM155_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336986 WCM156_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330246 WCM156_1_C_WES_Tumor WCM156_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336987 WCM161_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330247 WCM161_1_N_WES_Tumor WCM161_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336988 WCM192_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330248 WCM192_1_N_WES_Tumor WCM192_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336989 WCM198_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330249 WCM198_1_N_WES_Tumor WCM198_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336990 WCM199_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330250 WCM199_1_C_WES_Tumor WCM199_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336991 WCM207_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330251 WCM207_1_N_WES_Tumor WCM207_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336992 WCM209_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330252 WCM209_1_C_WES_Tumor WCM209_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336993 WCM210_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330253 WCM210_1_N_WES_Tumor WCM210_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336994 WCM213_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330254 WCM213_1_C_WES_Tumor WCM213_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336995 WCM221_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330255 WCM221_1_C_WES_Tumor WCM221_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336996 WCM252_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330256 WCM252_1_N_WES_Tumor WCM252_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336997 WCM253_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330257 WCM253_1_C_WES_Tumor WCM253_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336998 WCM340_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330258 WCM340_1_N_WES_Tumor WCM340_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5336999 WCM341_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330259 WCM341_1_C_WES_Tumor WCM341_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337000 WCM343_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330260 WCM343_1_C_WES_Tumor WCM343_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337001 WCM367_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330261 WCM367_1_C_WES_Tumor WCM367_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337002 WCM373_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330262 WCM373_1_C_WES_Tumor WCM373_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337003 WCM405_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330263 WCM405_1_C_WES_Tumor WCM405_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337004 WCM423_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330264 WCM423_1_C_WES_Tumor WCM423_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337005 WCM509_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330265 WCM509_1_C_WES_Tumor WCM509_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337006 WCM554_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330266 WCM554_1_C_WES_Tumor WCM554_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337007 WCM555_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330267 WCM555_1_C_WES_Tumor WCM555_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337008 WCM556_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330268 WCM556_1_C_WES_Tumor WCM556_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337009 WCM572_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330269 WCM572_1_C_WES_Tumor WCM572_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337010 WCM573_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330270 WCM573_1_N_WES_Tumor WCM573_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337011 WCM6_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330271 WCM6_1_C_WES_Tumor WCM6_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337012 WCM646_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330272 WCM646_1_N_WES_Tumor WCM646_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337013 WCM647_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330273 WCM647_1_N_WES_Tumor WCM647_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337014 WCM648_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330274 WCM648_1_C_WES_Tumor WCM648_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337015 WCM650_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330275 WCM650_1_N_WES_Tumor WCM650_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337016 WCM653_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330276 WCM653_1_N_WES_Tumor WCM653_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337017 WCM654_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330277 WCM654_1_N_WES_Tumor WCM654_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337018 WCM655_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330278 WCM655_1_N_WES_Tumor WCM655_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337019 WCM657_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330279 WCM657_1_C_WES_Tumor WCM657_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337020 WCM658_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330280 WCM658_1_N_WES_Tumor WCM658_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337021 WCM662_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330281 WCM662_1_C_WES_Tumor WCM662_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337022 WCM663_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330282 WCM663_1_C_WES_Tumor WCM663_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337023 WCM664_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330283 WCM664_1_C_WES_Tumor WCM664_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337024 WCM665_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330862 WCM665_1_N_WES_Tumor WCM665_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337025 WCM666_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330863 WCM666_1_N_WES_Tumor WCM666_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337026 WCM668_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330864 WCM668_1_C_WES_Tumor WCM668_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337027 WCM688_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330865 WCM688_1_N_WES_Tumor WCM688_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337028 WCM733_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330866 WCM733_1_C_WES_Tumor WCM733_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337029 WCM78_1_C_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330710 WCM78_1_C_WES_Tumor WCM78_1_C_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337030 WCM886_1_N_WES_Tumor SRP183790 phs001666 DNA was extracted using Promega Maxwell 16 MDx. DNA was stored at −20 degrees Celsius. Whole exome capture libraries were constructed from tumor and normal tissue after sample shearing, end repair, and phosphorylation and ligation to barcoded sequencing adaptors. Ligated DNA was size selected for lengths between 200-350 bp and subjected to exonic hybrid capture using HaloPlex Exome (Agilent) Version A SRS4330284 WCM886_1_N_WES_Tumor WCM886_1_N_WES_Tumor WXS GENOMIC unspecified 200 0 Application Read Forward 1 1 Application Read Reverse 101 Illumina HiSeq 2500 SRX5337031 WCM155_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330285 WCM155_1_N_RNA_Tumor WCM155_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337032 WCM161_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330286 WCM161_1_N_RNA_Tumor WCM161_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337033 WCM192_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330287 WCM192_1_N_RNA_Tumor WCM192_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337034 WCM209_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330288 WCM209_1_C_RNA_Tumor WCM209_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337035 WCM210_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330289 WCM210_1_N_RNA_Tumor WCM210_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337036 WCM213_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330290 WCM213_1_C_RNA_Tumor WCM213_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337037 WCM252_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330291 WCM252_1_N_RNA_Tumor WCM252_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337038 WCM341_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330709 WCM341_1_C_RNA_Tumor WCM341_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337039 WCM373_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330711 WCM373_1_C_RNA_Tumor WCM373_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337040 WCM423_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330712 WCM423_1_C_RNA_Tumor WCM423_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337041 WCM556_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330713 WCM556_1_C_RNA_Tumor WCM556_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337042 WCM573_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330714 WCM573_1_N_RNA_Tumor WCM573_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337043 WCM665_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330715 WCM665_1_N_RNA_Tumor WCM665_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337044 WCM666_1_N_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330716 WCM666_1_N_RNA_Tumor WCM666_1_N_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500 SRX5337045 WCM733_1_C_RNA_Tumor SRP183790 phs001666 RNA was extracted from frozen material for RNA-sequencing (RNA-seq) using Promega Maxwell 16 MDx instrument, (Maxwell 16 LEV simplyRNA Tissue Kit (Cat. # AS1280)). Specimens were prepared for RNA sequencing using TruSeq RNA Library Preparation Kit v2. RNA integrity was verified using the Agilent Bioanalyzer 2100 (Agilent Technologies). SRS4330717 WCM733_1_C_RNA_Tumor WCM733_1_C_RNA_Tumor RNA-Seq TRANSCRIPTOMIC unspecified 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina HiSeq 2500