SRX856955 Sample P2F SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829024 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.70 GATK 1.6 SRX857040 Sample P1 SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829088 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.70 GATK 1.6 SRX857041 Sample P1M SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829089 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.70 GATK 1.6 SRX857042 P2M SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829090 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.7 GATK 1.6 SRX857043 Sample P2 SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829091 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.7 GATK 1.6 SRX857045 Sample P1F SRP052905 Genomic DNA was extracted from lymphoblastoid cell lines. Genomic DNA was fragmented and 500 bp fragments were size selected using gel electrophoresis. Adaptor sequences were the ligated. Sequencing was performed on the Illumina HiSeq 2000 platform to generate 90 bp paired-end reads. Reads were mapped to the human reference genome (hg19) using Burrows Wheeler Aligner (BWA) and duplicate reads were filtered using Picard. SRS829093 WGS GENOMIC size fractionation 180 0 Application Read Forward 1 1 Application Read Reverse 91 Illumina HiSeq 2000 BWA 0.5.9-r16 Picard 1.7 GATK 1.6