SRX3204976 PA_BB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531037 PA_BB PA_BB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204977 PA_LB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531038 PA_LB PA_LB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204978 SG_JB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531039 SG_JB SG_JB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204979 SG_SP SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531041 SG_SP SG_SP WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204980 SG_BB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531040 SG_BB SG_BB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204981 SG_LB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531042 SG_LB SG_LB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204982 SG_PN SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531043 SG_PN SG_PN WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204983 SG_HB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531044 SG_HB SG_HB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204984 PA_JB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531045 PA_JB PA_JB WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204985 PA_SP SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531046 PA_SP PA_SP WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204986 PA_PN SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531047 PA_PN PA_PN WGS GENOMIC Reduced Representation Illumina MiSeq SRX3204987 PA_HB SRP118567 bp0 We used the ezRAD library preparation and sequencing approach (Toonen et al. 2013), which uses high-frequency cutter isochimozer enzymes MboI and Sau3AI (which cut the same site) to perform a DNA double digest. Digestion and library preparation protocols were the same of those described in Toonen et al. (2013). Briefly, the digested DNA is inserted into an Illumina TruSeq library preparation kit, where the digesting libraries are end-repaired and TruSeq adapters are ligated to the genomic fragments. Libraries are then size-selected on a 2100 Agilent Bioanalzer, quantified using qPCR (following Kapabiosystems Illumina quantification kit protocol), and paired end sequencing using 600 cycles on the Illumina Mi-Seq platform. Ê SRS2531048 PA_HB PA_HB WGS GENOMIC Reduced Representation Illumina MiSeq