SRX18332006 GSM6745804_r1 SRP409009 PRJNA903906 SRS15821071 GSM6745804 GSM6745804 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332007 GSM6745805_r1 SRP409009 PRJNA903906 SRS15821072 GSM6745805 GSM6745805 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332008 GSM6745806_r1 SRP409009 PRJNA903906 SRS15821074 GSM6745806 GSM6745806 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332009 GSM6745807_r1 SRP409009 PRJNA903906 SRS15821073 GSM6745807 GSM6745807 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332010 GSM6745808_r1 SRP409009 PRJNA903906 SRS15821075 GSM6745808 GSM6745808 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332011 GSM6745809_r1 SRP409009 PRJNA903906 SRS15821076 GSM6745809 GSM6745809 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332012 GSM6745810_r1 SRP409009 PRJNA903906 SRS15821077 GSM6745810 GSM6745810 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332013 GSM6745811_r1 SRP409009 PRJNA903906 SRS15821078 GSM6745811 GSM6745811 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332014 GSM6745812_r1 SRP409009 PRJNA903906 SRS15821079 GSM6745812 GSM6745812 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332015 GSM6745813_r1 SRP409009 PRJNA903906 SRS15821081 GSM6745813 GSM6745813 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332016 GSM6745814_r1 SRP409009 PRJNA903906 SRS15821080 GSM6745814 GSM6745814 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332017 GSM6745815_r1 SRP409009 PRJNA903906 SRS15821082 GSM6745815 GSM6745815 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332018 GSM6745816_r1 SRP409009 PRJNA903906 SRS15821083 GSM6745816 GSM6745816 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332019 GSM6745817_r1 SRP409009 PRJNA903906 SRS15821084 GSM6745817 GSM6745817 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332020 GSM6745818_r1 SRP409009 PRJNA903906 SRS15821085 GSM6745818 GSM6745818 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000 SRX18332021 GSM6745819_r1 SRP409009 PRJNA903906 SRS15821086 GSM6745819 GSM6745819 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested at an OD of 0.6 by centrifugation for 2 min at 4°C. The cells were first broken by shaking in a Fastprep apparatus for 2 x 30 sec in the presence of one gram of 0.1-mm diameter glass Sigma beads, then treated with Trizol reagent, chloroform/ isoamylalcohol and precipitated with isopropanol. The pellet was resuspended in TE RNA libraries were prepared for sequencing using standard Illumina protocols Illumina stranded Total RNA prep Ligation kit with RiboZero Plus NextSeq 2000