SRX11358756 GSM5419301 SRP327094 SRS9405229 GSM5419301 RNA-Seq TRANSCRIPTOMIC cDNA Naïve CD8+T cells were isolated by FACS, followed by activation with anti-CD3 and CD28 antibody for 18hr in vitro. RNA was extracted using Trizol reagent. 1 ug of total RNA was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305419301 GSM5419301 GEO Accession GSM5419301 SRX11358757 GSM5419302 SRP327094 SRS9405230 GSM5419302 RNA-Seq TRANSCRIPTOMIC cDNA Naïve CD8+T cells were isolated by FACS, followed by activation with anti-CD3 and CD28 antibody for 18hr in vitro. RNA was extracted using Trizol reagent. 1 ug of total RNA was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305419302 GSM5419302 GEO Accession GSM5419302 SRX11358758 GSM5419303 SRP327094 SRS9405231 GSM5419303 RNA-Seq TRANSCRIPTOMIC cDNA Naïve CD8+T cells were isolated by FACS, followed by activation with anti-CD3 and CD28 antibody for 18hr in vitro. RNA was extracted using Trizol reagent. 1 ug of total RNA was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305419303 GSM5419303 GEO Accession GSM5419303 SRX11358759 GSM5419304 SRP327094 SRS9405232 GSM5419304 RNA-Seq TRANSCRIPTOMIC cDNA Naïve CD8+T cells were isolated by FACS, followed by activation with anti-CD3 and CD28 antibody for 18hr in vitro. RNA was extracted using Trizol reagent. 1 ug of total RNA was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305419304 GSM5419304 GEO Accession GSM5419304