SRX5248953 GSM3562357 SRP179110 SRS4251128 GSM3562357 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562357 GSM3562357 GEO Accession GSM3562357 SRX5248954 GSM3562358 SRP179110 SRS4251129 GSM3562358 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562358 GSM3562358 GEO Accession GSM3562358 SRX5248955 GSM3562359 SRP179110 SRS4251130 GSM3562359 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562359 GSM3562359 GEO Accession GSM3562359 SRX5248956 GSM3562360 SRP179110 SRS4251131 GSM3562360 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562360 GSM3562360 GEO Accession GSM3562360 SRX5248957 GSM3562361 SRP179110 SRS4251132 GSM3562361 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562361 GSM3562361 GEO Accession GSM3562361 SRX5248958 GSM3562362 SRP179110 SRS4251133 GSM3562362 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted and digested by DNase I, then quantification and qualification were performed and checked before next step. cDNA libraries were constructed using NEBNext® UltraTM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer's recommendations. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturer's instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq platform and 125 bp/150 bp paired-end reads were generated Illumina HiSeq 2000 gds 303562362 GSM3562362 GEO Accession GSM3562362