ERX2932570 E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep1_s E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep1_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912814 SAMEA5128429 HH7LVBGXY_wildtype_treated_rep1_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: dose 10 Experimental Factor: compound sodium crotonate ERX2932571 E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep2_s E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep2_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912815 SAMEA5128430 HH7LVBGXY_wildtype_treated_rep2_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: dose 10 Experimental Factor: compound sodium crotonate ERX2932572 E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep3_s E-MTAB-7471:HH7LVBGXY_wildtype_treated_rep3_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912816 SAMEA5128431 HH7LVBGXY_wildtype_treated_rep3_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: dose 10 Experimental Factor: compound sodium crotonate ERX2932573 E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep1_s E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep1_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912817 SAMEA5128432 HH7LVBGXY_wildtype_untreated_rep1_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: compound none ERX2932574 E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep2_s E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep2_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912818 SAMEA5128433 HH7LVBGXY_wildtype_untreated_rep2_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: compound none ERX2932575 E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep3_s E-MTAB-7471:HH7LVBGXY_wildtype_untreated_rep3_s ERP112286 PRJEB29927 RNA-seq in wild-type Saccharomyces cerevisiae S288c cells to determine the effect of sodium crotonate treatment on the transcriptome ERS2912819 SAMEA5128434 HH7LVBGXY_wildtype_untreated_rep3_s RNA-Seq TRANSCRIPTOMIC Oligo-dT Three independent yeast colonies were used for inoculation. Overnight cultures were diluted in fresh medium with or without 10 mM sodium crotonate (Sigma-Aldrich) in the presence of 0.8 M sorbitol (Sigma-Aldrich). After 3.5 hours cells were in early log-phase (1 × 10^7 cells/ml) and harvested by centrifugation. Total RNA was isolated using the RNeasyMini kit (Qiagen) and treated with the RNase-Free DNase Set (Qiagen) to remove any contaminating genomic DNA. Library preparations were performed with the TruSeq Stranded mRNA Library kit (Illumina). NextSeq 500 Experimental Factor: compound none