SRX2765943 GSM2589764 SRP105275 PRJNA384377 SRS2150030 SAMN06835249 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589764 GSM2589764 GEO Accession GSM2589764 SRX2765944 GSM2589765 SRP105275 PRJNA384377 SRS2150031 SAMN06835248 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589765 GSM2589765 GEO Accession GSM2589765 SRX2765945 GSM2589766 SRP105275 PRJNA384377 SRS2150033 SAMN06835247 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589766 GSM2589766 GEO Accession GSM2589766 SRX2765946 GSM2589767 SRP105275 PRJNA384377 SRS2150032 SAMN06835246 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589767 GSM2589767 GEO Accession GSM2589767 SRX2765947 GSM2589768 SRP105275 PRJNA384377 SRS2150034 SAMN06835245 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589768 GSM2589768 GEO Accession GSM2589768 SRX2765948 GSM2589769 SRP105275 PRJNA384377 SRS2150035 SAMN06835244 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589769 GSM2589769 GEO Accession GSM2589769 SRX2765949 GSM2589770 SRP105275 PRJNA384377 SRS2150036 SAMN06835243 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589770 GSM2589770 GEO Accession GSM2589770 SRX2765950 GSM2589771 SRP105275 PRJNA384377 SRS2150037 SAMN06835242 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extacted using TRIsure (BIOLINE, London, UK) and treated with Rnase-free DNase (Promega, Madison). Two and a half micrograms of total RNA was subjected to ribosomal RNA depletion using Ribo-Zero Magnetic Gold Kit (Human/Mouse/Rat) (Epicentre) followed by RNA-seq library preparation using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB) according to the manufacturer's instructions. Each library was quantified using Kapa Library Quantitation Kit (Kappa) and sequenced on Illumina HiSeq2500 to generate 101-bp paired-end reads. Illumina HiSeq 2500 gds 302589771 GSM2589771 GEO Accession GSM2589771