SRX18711267 303988 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150438 P1_Blood 303988 WXS GENOMIC PCR HiSeq X Ten SRX18711268 303989 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150439 P1_OLK 303989 WXS GENOMIC PCR HiSeq X Ten SRX18711269 303990 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150440 P2_Blood 303990 WXS GENOMIC PCR HiSeq X Ten SRX18711270 303991 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150441 P2_OLK 303991 WXS GENOMIC PCR HiSeq X Ten SRX18711271 336604 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150442 P3_Blood 336604 WXS GENOMIC PCR HiSeq X Ten SRX18711272 336605 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150443 P3_OLK 336605 WXS GENOMIC PCR HiSeq X Ten SRX18711273 SO9756A03 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150444 P4_Blood SO9756A03 WXS GENOMIC PCR HiSeq X Ten SRX18711274 SO9756B03 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150445 P4_OLK SO9756B03 WXS GENOMIC PCR HiSeq X Ten SRX18711275 SO9756C03 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150446 P5_Blood SO9756C03 WXS GENOMIC PCR HiSeq X Ten SRX18711276 SO9756D03 SRP413223 bp0 WXS library was prepared from the sample using Agilent-SureSelectXT Human All Exon V5. Biotinylated oligonucleotide capture probes were used to enrich the whole exome by hybridization. The workflow involved shearing of DNA, repairing ends, adenylation of 3' ends, followed by adapter ligation to generate paired-end libraries. The resulting libraries were purified, quantified, and hybridized with exome-specific biotinylated capture library. The resulting enriched DNA libraries were multiplexed by adding index tags by amplification, followed by purification. SRS16150447 P5_OLK SO9756D03 WXS GENOMIC PCR HiSeq X Ten