SRX2568280 HIHG_S_1_13_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984636 S_1_13 HIHG_S_1_13_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568281 HIHG_S_1_41_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984637 S_1_41 HIHG_S_1_41_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568282 HIHG_S_1_5_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984638 S_1_5 HIHG_S_1_5_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568283 HIHG_S_1_57_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984639 S_1_57 HIHG_S_1_57_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568284 HIHG_S_1_78_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984640 S_1_78 HIHG_S_1_78_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568285 HIHG_S_1_79_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984641 S_1_79 HIHG_S_1_79_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568286 HIHG_S_1_80_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984642 S_1_80 HIHG_S_1_80_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568287 HIHG_S_1_86_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984643 S_1_86 HIHG_S_1_86_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568288 HIHG_S_1_88_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984644 S_1_88 HIHG_S_1_88_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000 SRX2568289 HIHG_S_1_99_ILLU SRP089737 phs001046 "Preparation was done on two Perkin Elmer Sciclone G3 and one Zephyr liquid handling workstations. Samples were processed in 96 well plates. DNA was then quantitated using the Qubit dsDNA Assay.Samples are then queued for library preparation and target enrichment according to the Agilent SureSelect XT Target Enrichment protocol for Illumina Paired End sequencing. Sequencing was done using Illumina Hiseq 2000. Data processing is done first using Hiseq Real Time Analysis software Casava (if this fails Bustard is used instead), then files turned into zipped fastq files with raw read and base qualities.Fastq sequences are aligned to hg19 with Burrows-Wheeler Aligner." SRS1984645 S_1_99 HIHG_S_1_99_ILLU WXS GENOMIC Hybrid Selection 198 0 Application Read Forward 1 1 Application Read Reverse 100 Illumina HiSeq 2000