SRX17889285 GSM6638255_r1 SRP402639 PRJNA890575 SRS15406492 GSM6638255 GSM6638255 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889286 GSM6638256_r1 SRP402639 PRJNA890575 SRS15406493 GSM6638256 GSM6638256 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889287 GSM6638257_r1 SRP402639 PRJNA890575 SRS15406494 GSM6638257 GSM6638257 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889288 GSM6638258_r1 SRP402639 PRJNA890575 SRS15406495 GSM6638258 GSM6638258 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889289 GSM6638259_r1 SRP402639 PRJNA890575 SRS15406496 GSM6638259 GSM6638259 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889290 GSM6638260_r1 SRP402639 PRJNA890575 SRS15406497 GSM6638260 GSM6638260 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889291 GSM6638261_r1 SRP402639 PRJNA890575 SRS15406498 GSM6638261 GSM6638261 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889292 GSM6638262_r1 SRP402639 PRJNA890575 SRS15406499 GSM6638262 GSM6638262 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889293 GSM6638263_r1 SRP402639 PRJNA890575 SRS15406500 GSM6638263 GSM6638263 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889294 GSM6638264_r1 SRP402639 PRJNA890575 SRS15406501 GSM6638264 GSM6638264 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889295 GSM6638265_r1 SRP402639 PRJNA890575 SRS15406502 GSM6638265 GSM6638265 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889296 GSM6638266_r1 SRP402639 PRJNA890575 SRS15406503 GSM6638266 GSM6638266 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889297 GSM6638267_r1 SRP402639 PRJNA890575 SRS15406504 GSM6638267 GSM6638267 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889298 GSM6638268_r1 SRP402639 PRJNA890575 SRS15406505 GSM6638268 GSM6638268 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000 SRX17889299 GSM6638269_r1 SRP402639 PRJNA890575 SRS15406506 GSM6638269 GSM6638269 RNA-Seq TRANSCRIPTOMIC cDNA Naïve (CD44−CD62L+) CD8+ T cells were sorted from Mettl3ΔCd4 and control mice (3 samples per group), effector (CD44+CD62L−EYFP+) CD8+ T cells (2 samples per group), and memory (CD44+EYFP+) CD8+ T cells (2 samples from control donors and 3 samples from Mettl3ΔGzmb donors ) were sorted from recipient mice in adoptive transfer experiments. Total RNAs were extracted from indicated cells and then submitted to RNA-Seq protocol. libraries are constructed according to the standard protocol for Smart-seq2 Illumina NovaSeq 6000