SRX4328982 GSM3239802 SRP151710 SRS3491029 GSM3239802 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated and rRNAs were depleted using the Ribo-Zero Gram-Positive rRNA Removal Kit (Epicentre). The rRNA-depleted RNA was used to generate cDNA libraries using the ScriptSeq kit (Epicentre). Briefly, RNA was fragmented, cDNA was synthesized using random hexamers containing a 5′ tagging sequence, the RNA was hydrolyzed, and the cDNA was tagged at the 3′ end. A limited number of PCR cycles (n=12) were used to amplify the libraries via the 5′ and 3′ tags (the libraries were barcoded by using different primers), and the libraries size-selected (170 to 300 bp). The size-selected and barcoded libraries were run on an Illumina HiSeq flowcell. Illumina HiSeq 2500 gds 303239802 GSM3239802 GEO Accession GSM3239802 SRX4328983 GSM3239803 SRP151710 SRS3491030 GSM3239803 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated and rRNAs were depleted using the Ribo-Zero Gram-Positive rRNA Removal Kit (Epicentre). The rRNA-depleted RNA was used to generate cDNA libraries using the ScriptSeq kit (Epicentre). Briefly, RNA was fragmented, cDNA was synthesized using random hexamers containing a 5′ tagging sequence, the RNA was hydrolyzed, and the cDNA was tagged at the 3′ end. A limited number of PCR cycles (n=12) were used to amplify the libraries via the 5′ and 3′ tags (the libraries were barcoded by using different primers), and the libraries size-selected (170 to 300 bp). The size-selected and barcoded libraries were run on an Illumina HiSeq flowcell. Illumina HiSeq 2500 gds 303239803 GSM3239803 GEO Accession GSM3239803 SRX4328984 GSM3239804 SRP151710 SRS3491031 GSM3239804 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated and rRNAs were depleted using the Ribo-Zero Gram-Positive rRNA Removal Kit (Epicentre). The rRNA-depleted RNA was used to generate cDNA libraries using the ScriptSeq kit (Epicentre). Briefly, RNA was fragmented, cDNA was synthesized using random hexamers containing a 5′ tagging sequence, the RNA was hydrolyzed, and the cDNA was tagged at the 3′ end. A limited number of PCR cycles (n=12) were used to amplify the libraries via the 5′ and 3′ tags (the libraries were barcoded by using different primers), and the libraries size-selected (170 to 300 bp). The size-selected and barcoded libraries were run on an Illumina HiSeq flowcell. Illumina HiSeq 2500 gds 303239804 GSM3239804 GEO Accession GSM3239804 SRX4328985 GSM3239805 SRP151710 SRS3491032 GSM3239805 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated and rRNAs were depleted using the Ribo-Zero Gram-Positive rRNA Removal Kit (Epicentre). The rRNA-depleted RNA was used to generate cDNA libraries using the ScriptSeq kit (Epicentre). Briefly, RNA was fragmented, cDNA was synthesized using random hexamers containing a 5′ tagging sequence, the RNA was hydrolyzed, and the cDNA was tagged at the 3′ end. A limited number of PCR cycles (n=12) were used to amplify the libraries via the 5′ and 3′ tags (the libraries were barcoded by using different primers), and the libraries size-selected (170 to 300 bp). The size-selected and barcoded libraries were run on an Illumina HiSeq flowcell. Illumina HiSeq 2500 gds 303239805 GSM3239805 GEO Accession GSM3239805