SRX23225591 AHLA SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148773 AHLA AHLA WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225592 FJZZ SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148774 FJZZ FJZZ WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225593 GDSG SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148775 GDSG GDSG WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225594 GXQZ SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148776 GXQZ GXQZ WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225595 HeNXY SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148777 HeNXY HeNXY WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225596 HuNXX SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148778 HuNXX HuNXX WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225597 JSYX SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148779 JSYX JSYX WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225598 SCEM SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148780 SCEM SCEM WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225599 TWXB SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148782 TWXB TWXB WGS GENOMIC RANDOM DNBSEQ-T7 SRX23225600 ZJLS SRP483860 bp0 Approximately 1 g genomic DNA was broken into small fragments using the Covaris E210 sonicator (Covaris Inc., MA, USA). Fragments were then size-selected selected by Agencourt AMPure XP-Medium kit (Thermo Fisher Scientific, USA) to attain sizes ranging from 200 to 400 bp. Following end repair, 3adenylation, adaptor ligation, PCR amplification, and purification, the resulting double-stranded PCR products were transformed into single-stranded circular DNA (ssCir DNA), through heat denaturation and circularization using a splint oligo sequence. The ssCir DNA was formatted as the final library, and sequenced on DNBSEQ-T7 sequencing platform to generate 150-bp paired-end reads. SRS20148781 ZJLS ZJLS WGS GENOMIC RANDOM DNBSEQ-T7