ERX240934 E-SYBR-10:M28-4D ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241145 SAMEA2064789 E-SYBR-10:M28-4D M28-4D WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-4D ERX240935 E-SYBR-10:M28-1B ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241146 SAMEA2064790 E-SYBR-10:M28-1B M28-1B WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-1B ERX240936 E-SYBR-10:M28-4A ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241147 SAMEA2064791 E-SYBR-10:M28-4A M28-4A WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-4A ERX240937 E-SYBR-10:M28-2D ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241148 SAMEA2064792 E-SYBR-10:M28-2D M28-2D WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-2D ERX240938 E-SYBR-10:M28-2C ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241149 SAMEA2064793 E-SYBR-10:M28-2C M28-2C WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-2C ERX240939 E-SYBR-10:M28-1A ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241150 SAMEA2064794 E-SYBR-10:M28-1A M28-1A WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-1A ERX240940 E-SYBR-10:M28-2B ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241151 SAMEA2064795 E-SYBR-10:M28-2B M28-2B WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-2B ERX240941 E-SYBR-10:M28-1C ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241152 SAMEA2064796 E-SYBR-10:M28-1C M28-1C WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-1C ERX240942 E-SYBR-10:M28-4B ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241153 SAMEA2064797 E-SYBR-10:M28-4B M28-4B WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-4B ERX240943 E-SYBR-10:M28-1D ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241154 SAMEA2064798 E-SYBR-10:M28-1D M28-1D WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-1D ERX240944 E-SYBR-10:M28-4C ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241155 SAMEA2064929 E-SYBR-10:M28-4C M28-4C WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-4C ERX240945 E-SYBR-10:M28-2A ERP002542 E-SYBR-10 Whole genome sequence for S. cerevisiae strains. ERS241156 SAMEA2064930 E-SYBR-10:M28-2A M28-2A WGS GENOMIC size fractionation Montalcino Grape, Cavalieri et al 2000 (PMID: 11035792). Cells were grown in YPD liquid medium for genomic DNA extraction DNA was extracted from 10 raise to 9 pelleted cells with the Qiagen "Genomic DNA Isolation Kit" following the manufacturer's instructions. Libraries were constructed using Illumina TruSeq DNA Sample Prep standard protocol. Briefly, 5 ug of high molecular weight genomic DNA (gDNA) was fragmented by Covaris sonication device. Following sonication, DNA fragments were end-repaired and A-tailed. Adapters were then ligated via a 3 prime thymine overhang. Finally, ligated fragments were amplified by PCR (10 cycles). insert sizes were about 400-500 bp as evaluated in an Agilent DNA 1000 Analyzer Chip. Illumina HiSeq 2000 Experimental Factor: strain M28-2A