ERS1237208 SAMEA4066098 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066098 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 1 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 1 strain wild type genotype ERS1237209 SAMEA4066099 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066099 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 10 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 10 strain wild type genotype ERS1237210 SAMEA4066100 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066100 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 11 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 11 strain npl3-1 ERS1237211 SAMEA4066101 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066101 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 12 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 12 strain npl3-1 ERS1237212 SAMEA4066102 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066102 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 13 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 13 strain wild type genotype ERS1237213 SAMEA4066103 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066103 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 14 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 14 strain wild type genotype ERS1237214 SAMEA4066104 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066104 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 15 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 15 strain wild type genotype ERS1237215 SAMEA4066105 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066105 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 16 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 16 strain wild type genotype ERS1237216 SAMEA4066106 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066106 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 17 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 17 strain npl3-1 ERS1237217 SAMEA4066107 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066107 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 18 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 18 strain npl3-1 ERS1237218 SAMEA4066108 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066108 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 2 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 2 strain wild type genotype ERS1237219 SAMEA4066109 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066109 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 3 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 3 strain wild type genotype ERS1237220 SAMEA4066110 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066110 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 4 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 4 strain wild type genotype ERS1237221 SAMEA4066111 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066111 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 5 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 5 strain npl3-1 ERS1237222 SAMEA4066112 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066112 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 6 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 6 strain npl3-1 ERS1237223 SAMEA4066113 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066113 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 7 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 7 strain wild type genotype ERS1237224 SAMEA4066114 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066114 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 8 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 8 strain wild type genotype ERS1237225 SAMEA4066115 4932 Saccharomyces cerevisiae Protocols: Isw1-PrA expressing cells were grown overnight at 25°C and shifted for 3 hours at 30°C. RNA immunoprecipitations were performed from 2g of frozen cell grindates prepared as previously described (Oeffinger et al., 2007). Immunoprecipitated RNA was isolated from proteins by treating samples with 40 μg Proteinase K (Roche) and 0,1% SDS for 30 min at 30 °C. RNA was extracted with the Nucleospin RNA II Kit (Macherey-Nagel), Libraries were prepared using the strand specific RNA-Seq library preparation TruSeq Stranded mRNA kit (Illumina). Libraries were multiplexed by 9 on 2 flowcell lanes. A 50 bp read sequencing was performed on a HiSeq 1500 device (Illumina). A mean of 22.9 ± 2.6 million passing Illumina quality filter reads was obtained for each of the 18 samples. Library preparation and Illumina sequencing were performed at the Ecole Normale Supérieure Genomic Platform (Paris, France). ENA first public 2016-11-17 ENA last update 2016-07-06 External Id SAMEA4066115 INSDC center alias INSERM INSDC center name INSERM INSDC first public 2016-11-17T17:05:05Z INSDC last update 2016-07-06T15:04:08Z INSDC status public Submitter Id E-MTAB-4826:Sample 9 broker name ArrayExpress common name baker's yeast sample name E-MTAB-4826:Sample 9 strain wild type genotype