SRX13166238 GSM5694704_r1 SRP346754 PRJNA781589 SRS11097291 GSM5694704 GSM5694704 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166239 GSM5694705_r1 SRP346754 PRJNA781589 SRS11097292 GSM5694705 GSM5694705 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166240 GSM5694706_r1 SRP346754 PRJNA781589 SRS11097293 GSM5694706 GSM5694706 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166241 GSM5694707_r1 SRP346754 PRJNA781589 SRS11097294 GSM5694707 GSM5694707 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166242 GSM5694708_r1 SRP346754 PRJNA781589 SRS11097295 GSM5694708 GSM5694708 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166243 GSM5694709_r1 SRP346754 PRJNA781589 SRS11097296 GSM5694709 GSM5694709 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166244 GSM5694710_r1 SRP346754 PRJNA781589 SRS11097297 GSM5694710 GSM5694710 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166245 GSM5694711_r1 SRP346754 PRJNA781589 SRS11097298 GSM5694711 GSM5694711 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166246 GSM5694712_r1 SRP346754 PRJNA781589 SRS11097299 GSM5694712 GSM5694712 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166247 GSM5694713_r1 SRP346754 PRJNA781589 SRS11097300 GSM5694713 GSM5694713 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166248 GSM5694714_r1 SRP346754 PRJNA781589 SRS11097301 GSM5694714 GSM5694714 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166249 GSM5694715_r1 SRP346754 PRJNA781589 SRS11097302 GSM5694715 GSM5694715 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166250 GSM5694716_r1 SRP346754 PRJNA781589 SRS11097303 GSM5694716 GSM5694716 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166251 GSM5694717_r1 SRP346754 PRJNA781589 SRS11097304 GSM5694717 GSM5694717 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166252 GSM5694718_r1 SRP346754 PRJNA781589 SRS11097306 GSM5694718 GSM5694718 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000 SRX13166253 GSM5694719_r1 SRP346754 PRJNA781589 SRS11097305 GSM5694719 GSM5694719 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Qiagen Rneasy kit following the manufacturer's instructions. Library Prep was performed with NEBNext E7530S following the manual, 11 cycles of PCR were performed for amplification. NEBNext E7335L was used for multiplexing. Quality control: the size and distribution were controlled on gel. RNA-Seq libraries were sequenced on Illumina HiSeq 3000 as 100-nt paired end reads. Illumina HiSeq 3000