SRX17905701 Mother_1010234 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422412 Mother_1010234 Mother_1010234 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905702 Father_787 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422414 Father_787 Father_787 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905703 F2P1_DR_A6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422413 F2P1_DR_A6 F2P1_DR_A6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905704 F2P2_DS_D5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422415 F2P2_DS_D5 F2P2_DS_D5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905705 F2P2_DS_D6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422417 F2P2_DS_D6 F2P2_DS_D6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905706 F2P2_DS_D7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422416 F2P2_DS_D7 F2P2_DS_D7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905707 F2P2_DS_D9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422418 F2P2_DS_D9 F2P2_DS_D9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905708 F2P2_DS_E1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422420 F2P2_DS_E1 F2P2_DS_E1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905709 F2P2_DS_E2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422419 F2P2_DS_E2 F2P2_DS_E2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905710 F2P2_DS_E3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422421 F2P2_DS_E3 F2P2_DS_E3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905711 F2P2_DS_E4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422422 F2P2_DS_E4 F2P2_DS_E4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905712 F2P2_DS_E6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422423 F2P2_DS_E6 F2P2_DS_E6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905713 F2P2_DS_E7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422424 F2P2_DS_E7 F2P2_DS_E7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905714 F2P1_DR_A7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422425 F2P1_DR_A7 F2P1_DR_A7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905715 F2P2_DS_F10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422426 F2P2_DS_F10 F2P2_DS_F10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905716 F2P2_DS_F11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422427 F2P2_DS_F11 F2P2_DS_F11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905717 F2P2_DS_F12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422428 F2P2_DS_F12 F2P2_DS_F12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905718 F2P2_DS_F1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422429 F2P2_DS_F1 F2P2_DS_F1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905719 F2P2_DS_F2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422430 F2P2_DS_F2 F2P2_DS_F2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905720 F2P2_DS_F3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422431 F2P2_DS_F3 F2P2_DS_F3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905721 F2P2_DS_F4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422432 F2P2_DS_F4 F2P2_DS_F4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905722 F2P2_DS_F5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422433 F2P2_DS_F5 F2P2_DS_F5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905723 F2P2_DS_F6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422434 F2P2_DS_F6 F2P2_DS_F6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905724 F2P2_DS_F7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422435 F2P2_DS_F7 F2P2_DS_F7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905725 F2P1_DR_E2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422436 F2P1_DR_E2 F2P1_DR_E2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905726 F2P1_DR_E3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422437 F2P1_DR_E3 F2P1_DR_E3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905727 F2P1_DR_E4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422438 F2P1_DR_E4 F2P1_DR_E4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905728 F2P1_DR_E5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422439 F2P1_DR_E5 F2P1_DR_E5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905729 F2P1_DR_E6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422440 F2P1_DR_E6 F2P1_DR_E6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905730 F2P1_DR_E7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422441 F2P1_DR_E7 F2P1_DR_E7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905731 F2P1_DR_E8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422442 F2P1_DR_E8 F2P1_DR_E8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905732 F2P1_DR_E9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422443 F2P1_DR_E9 F2P1_DR_E9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905733 F2P1_DR_F10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422444 F2P1_DR_F10 F2P1_DR_F10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905734 F2P1_DR_F11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422445 F2P1_DR_F11 F2P1_DR_F11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905735 F2P1_DR_A2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422446 F2P1_DR_A2 F2P1_DR_A2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905736 F2P1_DR_F12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422447 F2P1_DR_F12 F2P1_DR_F12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905737 F2P1_DR_F1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422448 F2P1_DR_F1 F2P1_DR_F1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905738 F2P1_DR_F2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422449 F2P1_DR_F2 F2P1_DR_F2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905739 F2P1_DR_F3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422450 F2P1_DR_F3 F2P1_DR_F3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905740 F2P1_DR_F4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422451 F2P1_DR_F4 F2P1_DR_F4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905741 F2P1_DR_F5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422452 F2P1_DR_F5 F2P1_DR_F5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905742 F2P1_DR_F6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422453 F2P1_DR_F6 F2P1_DR_F6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905743 F2P1_DR_F7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422454 F2P1_DR_F7 F2P1_DR_F7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905744 F2P1_DR_F8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422455 F2P1_DR_F8 F2P1_DR_F8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905745 F2P1_DR_F9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422456 F2P1_DR_F9 F2P1_DR_F9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905746 F2P1_DR_A3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422457 F2P1_DR_A3 F2P1_DR_A3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905747 F2P1_DR_G10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422458 F2P1_DR_G10 F2P1_DR_G10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905748 F2P1_DR_G11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422459 F2P1_DR_G11 F2P1_DR_G11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905749 F2P1_DR_A8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422460 F2P1_DR_A8 F2P1_DR_A8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905750 F2P2_DS_F8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422461 F2P2_DS_F8 F2P2_DS_F8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905751 F2P2_DS_F9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422462 F2P2_DS_F9 F2P2_DS_F9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905752 F2P2_DS_G12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422463 F2P2_DS_G12 F2P2_DS_G12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905753 F2P2_DS_G1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422464 F2P2_DS_G1 F2P2_DS_G1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905754 F2P2_DS_G2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422465 F2P2_DS_G2 F2P2_DS_G2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905755 F2P2_DS_G3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422466 F2P2_DS_G3 F2P2_DS_G3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905756 F2P2_DS_G4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422467 F2P2_DS_G4 F2P2_DS_G4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905757 F2P2_DS_G5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422468 F2P2_DS_G5 F2P2_DS_G5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905758 F2P2_DS_G6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422469 F2P2_DS_G6 F2P2_DS_G6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905759 F2P2_DS_G7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422470 F2P2_DS_G7 F2P2_DS_G7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905760 F2P1_DR_A9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422471 F2P1_DR_A9 F2P1_DR_A9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905761 F2P2_DS_G8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422472 F2P2_DS_G8 F2P2_DS_G8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905762 F2P2_DS_H10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422473 F2P2_DS_H10 F2P2_DS_H10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905763 F2P2_DS_H11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422474 F2P2_DS_H11 F2P2_DS_H11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905764 F2P2_DS_H12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422475 F2P2_DS_H12 F2P2_DS_H12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905765 F2P2_DS_H1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422476 F2P2_DS_H1 F2P2_DS_H1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905766 F2P2_DS_H2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422477 F2P2_DS_H2 F2P2_DS_H2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905767 F2P2_DS_H5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422479 F2P2_DS_H5 F2P2_DS_H5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905768 F2P2_DS_H6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422478 F2P2_DS_H6 F2P2_DS_H6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905769 F2P2_DS_H9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422480 F2P2_DS_H9 F2P2_DS_H9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905770 F2P3_DS_A11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422481 F2P3_DS_A11 F2P3_DS_A11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905771 F2P1_DR_B10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422482 F2P1_DR_B10 F2P1_DR_B10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905772 F2P3_DS_A12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422483 F2P3_DS_A12 F2P3_DS_A12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905773 F2P1_DR_G1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422484 F2P1_DR_G1 F2P1_DR_G1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905774 F2P1_DR_G2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422485 F2P1_DR_G2 F2P1_DR_G2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905775 F2P1_DR_G3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422486 F2P1_DR_G3 F2P1_DR_G3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905776 F2P1_DR_G4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422487 F2P1_DR_G4 F2P1_DR_G4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905777 F2P1_DR_G5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422488 F2P1_DR_G5 F2P1_DR_G5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905778 F2P1_DR_G6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422489 F2P1_DR_G6 F2P1_DR_G6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905779 F2P1_DR_G7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422490 F2P1_DR_G7 F2P1_DR_G7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905780 F2P1_DR_G8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422491 F2P1_DR_G8 F2P1_DR_G8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905781 F2P1_DR_A4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422492 F2P1_DR_A4 F2P1_DR_A4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905782 F2P1_DR_G9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422493 F2P1_DR_G9 F2P1_DR_G9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905783 F2P1_DR_H10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422494 F2P1_DR_H10 F2P1_DR_H10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905784 F2P1_DR_H11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422495 F2P1_DR_H11 F2P1_DR_H11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905785 F2P1_DR_H12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422496 F2P1_DR_H12 F2P1_DR_H12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905786 F2P1_DR_H1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422497 F2P1_DR_H1 F2P1_DR_H1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905787 F2P1_DR_H2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422498 F2P1_DR_H2 F2P1_DR_H2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905788 F2P1_DR_H3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422499 F2P1_DR_H3 F2P1_DR_H3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905789 F2P1_DR_H4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422500 F2P1_DR_H4 F2P1_DR_H4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905790 F2P1_DR_H5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422501 F2P1_DR_H5 F2P1_DR_H5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905791 F2P1_DR_H6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422502 F2P1_DR_H6 F2P1_DR_H6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905792 F2P1_DR_A5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422504 F2P1_DR_A5 F2P1_DR_A5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905793 F2P1_DR_H7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422503 F2P1_DR_H7 F2P1_DR_H7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905794 F2P1_DR_H8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422505 F2P1_DR_H8 F2P1_DR_H8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905795 F2P1_DR_H9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422506 F2P1_DR_H9 F2P1_DR_H9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905796 F2P2_DS_C8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422507 F2P2_DS_C8 F2P2_DS_C8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905797 F2P3_DS_A1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422508 F2P3_DS_A1 F2P3_DS_A1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905798 F2P3_DS_A2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422509 F2P3_DS_A2 F2P3_DS_A2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905799 F2P3_DS_A3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422510 F2P3_DS_A3 F2P3_DS_A3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905800 F2P3_DS_A4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422511 F2P3_DS_A4 F2P3_DS_A4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905801 F2P3_DS_A7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422512 F2P3_DS_A7 F2P3_DS_A7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905802 F2P3_DS_A8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422513 F2P3_DS_A8 F2P3_DS_A8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905803 F2P3_DS_A9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422514 F2P3_DS_A9 F2P3_DS_A9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905804 F2P3_DS_B10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422515 F2P3_DS_B10 F2P3_DS_B10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905805 F2P3_DS_B11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422516 F2P3_DS_B11 F2P3_DS_B11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905806 F2P1_DR_B11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422517 F2P1_DR_B11 F2P1_DR_B11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905807 F2P3_DS_B12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422518 F2P3_DS_B12 F2P3_DS_B12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905808 F2P3_DS_B1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422519 F2P3_DS_B1 F2P3_DS_B1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905809 F2P3_DS_B3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422520 F2P3_DS_B3 F2P3_DS_B3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905810 F2P3_DS_B4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422522 F2P3_DS_B4 F2P3_DS_B4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905811 F2P3_DS_B5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422521 F2P3_DS_B5 F2P3_DS_B5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905812 F2P3_DS_B6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422523 F2P3_DS_B6 F2P3_DS_B6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905813 F2P3_DS_B7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422524 F2P3_DS_B7 F2P3_DS_B7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905814 F2P3_DS_B8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422525 F2P3_DS_B8 F2P3_DS_B8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905815 F2P3_DS_C10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422526 F2P3_DS_C10 F2P3_DS_C10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905816 F2P3_DS_C11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422527 F2P3_DS_C11 F2P3_DS_C11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905817 F2P1_DR_B12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422528 F2P1_DR_B12 F2P1_DR_B12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905818 F2P3_DS_C12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422529 F2P3_DS_C12 F2P3_DS_C12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905819 F2P3_DS_C1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422530 F2P3_DS_C1 F2P3_DS_C1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905820 F2P3_DS_C3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422531 F2P3_DS_C3 F2P3_DS_C3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905821 F2P1_DR_C2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422532 F2P1_DR_C2 F2P1_DR_C2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905822 F2P1_DR_A11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422533 F2P1_DR_A11 F2P1_DR_A11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905823 F2P1_DR_C3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422534 F2P1_DR_C3 F2P1_DR_C3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905824 F2P1_DR_C4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422535 F2P1_DR_C4 F2P1_DR_C4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905825 F2P1_DR_C5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422536 F2P1_DR_C5 F2P1_DR_C5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905826 F2P1_DR_C6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422537 F2P1_DR_C6 F2P1_DR_C6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905827 F2P1_DR_C7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422538 F2P1_DR_C7 F2P1_DR_C7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905828 F2P1_DR_C8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422539 F2P1_DR_C8 F2P1_DR_C8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905829 F2P1_DR_C9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422540 F2P1_DR_C9 F2P1_DR_C9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905830 F2P1_DR_D10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422541 F2P1_DR_D10 F2P1_DR_D10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905831 F2P1_DR_D11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422542 F2P1_DR_D11 F2P1_DR_D11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905832 F2P1_DR_D12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422543 F2P1_DR_D12 F2P1_DR_D12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905833 F2P1_DR_A12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422544 F2P1_DR_A12 F2P1_DR_A12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905834 F2P1_DR_D1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422545 F2P1_DR_D1 F2P1_DR_D1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905835 F2P1_DR_D4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422546 F2P1_DR_D4 F2P1_DR_D4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905836 F2P1_DR_D5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422547 F2P1_DR_D5 F2P1_DR_D5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905837 F2P1_DR_D7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422548 F2P1_DR_D7 F2P1_DR_D7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905838 F2P1_DR_D8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422549 F2P1_DR_D8 F2P1_DR_D8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905839 F2P1_DR_D9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422550 F2P1_DR_D9 F2P1_DR_D9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905840 F2P1_DR_E10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422551 F2P1_DR_E10 F2P1_DR_E10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905841 F2P1_DR_E11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422552 F2P1_DR_E11 F2P1_DR_E11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905842 F2P1_DR_E12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422553 F2P1_DR_E12 F2P1_DR_E12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905843 F2P1_DR_E1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422554 F2P1_DR_E1 F2P1_DR_E1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905844 F2P1_DR_A1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422555 F2P1_DR_A1 F2P1_DR_A1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905845 F2P2_DS_D10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422556 F2P2_DS_D10 F2P2_DS_D10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905846 F2P2_DS_D11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422557 F2P2_DS_D11 F2P2_DS_D11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905847 F2P2_DS_D12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422558 F2P2_DS_D12 F2P2_DS_D12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905848 F2P2_DS_D2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422559 F2P2_DS_D2 F2P2_DS_D2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905849 F2P2_DS_D3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422560 F2P2_DS_D3 F2P2_DS_D3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905850 F2P2_DS_D4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422561 F2P2_DS_D4 F2P2_DS_D4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905851 F2P3_DS_C4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422562 F2P3_DS_C4 F2P3_DS_C4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905852 F2P3_DS_C5 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422563 F2P3_DS_C5 F2P3_DS_C5 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905853 F2P3_DS_C6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422564 F2P3_DS_C6 F2P3_DS_C6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905854 F2P3_DS_C7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422565 F2P3_DS_C7 F2P3_DS_C7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905855 F2P3_DS_C8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422566 F2P3_DS_C8 F2P3_DS_C8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905856 F2P3_DS_D1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422567 F2P3_DS_D1 F2P3_DS_D1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905857 F2P3_DS_D2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422568 F2P3_DS_D2 F2P3_DS_D2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905858 F2P1_DR_B1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422569 F2P1_DR_B1 F2P1_DR_B1 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905859 F2P3_DS_D3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422570 F2P3_DS_D3 F2P3_DS_D3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905860 F2P3_DS_D6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422571 F2P3_DS_D6 F2P3_DS_D6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905861 F2P3_DS_D8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422572 F2P3_DS_D8 F2P3_DS_D8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905862 F2P3_DS_D9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422573 F2P3_DS_D9 F2P3_DS_D9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905863 F2P1_DR_B2 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422574 F2P1_DR_B2 F2P1_DR_B2 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905864 F2P1_DR_B3 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422575 F2P1_DR_B3 F2P1_DR_B3 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905865 F2P1_DR_A10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422576 F2P1_DR_A10 F2P1_DR_A10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905866 F2P1_DR_B4 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422577 F2P1_DR_B4 F2P1_DR_B4 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905867 F2P1_DR_B6 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422579 F2P1_DR_B6 F2P1_DR_B6 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905868 F2P1_DR_B7 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422578 F2P1_DR_B7 F2P1_DR_B7 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905869 F2P1_DR_B8 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422580 F2P1_DR_B8 F2P1_DR_B8 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905870 F2P1_DR_B9 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422581 F2P1_DR_B9 F2P1_DR_B9 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905871 F2P1_DR_C10 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422582 F2P1_DR_C10 F2P1_DR_C10 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905872 F2P1_DR_C11 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422583 F2P1_DR_C11 F2P1_DR_C11 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905873 F2P1_DR_C12 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422584 F2P1_DR_C12 F2P1_DR_C12 RAD-Seq GENOMIC size fractionation NextSeq 500 SRX17905874 F2P1_DR_C1 SRP402860 bp0 In brief, 500 ng of DNA from each sample was double-digested with 20 units of EcoRI-HF and NIaIII (New England Biolabs, USA) for 30 min at 37C. Digested DNA fragments were examined by electrophoresis and then ligated with barcoded adaptors of P1 that contained a matching sticky-end and a MID (a short sequence that will uniquely identify the individuals) and P2. SRS15422585 F2P1_DR_C1 F2P1_DR_C1 RAD-Seq GENOMIC size fractionation NextSeq 500