SRX18057518 M1 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563574 S1 M1 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057519 M2 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563575 S2 M2 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057520 M14 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563576 S14 M14 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057521 M15 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563577 S12 M15 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057522 M16 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563578 S16 M16 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057523 VIIa SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563579 S41 VIIa WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057524 VIIb SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563580 S42 VIIb WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057525 XIIIb SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563581 S43 XIIIb WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057526 XIIIa SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563582 S44 XIIIa WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057527 WT SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563583 S20 WT WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057528 M3 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563585 S3 M3 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057529 M4 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563584 S4 M4 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057530 M5 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563586 S5 M5 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057531 M6 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563587 S6 M6 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057532 M8 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563588 S8 M8 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057533 M9 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563589 S9 M9 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057534 M10 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563590 S10 M10 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18057535 M11 SRP405032 bp0 The genomic DNA was randomly sheared into short fragments. The obtained fragments were end repaired, A-tailed and further ligated with Illumina adapter. The fragments with adapters were PCR amplified, size selected, and purified. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries were pooled and sequenced. SRS15563591 S11 M11 WGS GENOMIC RANDOM Illumina NovaSeq 6000