SRX23815960 GSM8123093_r1 SRP492975 PRJNA1083039 SRS20638524 GSM8123093 GSM8123093 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815961 GSM8123094_r1 SRP492975 PRJNA1083039 SRS20638525 GSM8123094 GSM8123094 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815962 GSM8123095_r1 SRP492975 PRJNA1083039 SRS20638526 GSM8123095 GSM8123095 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815963 GSM8123098_r1 SRP492975 PRJNA1083039 SRS20638527 GSM8123098 GSM8123098 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815964 GSM8123099_r1 SRP492975 PRJNA1083039 SRS20638528 GSM8123099 GSM8123099 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815965 GSM8123100_r1 SRP492975 PRJNA1083039 SRS20638529 GSM8123100 GSM8123100 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815966 GSM8123101_r1 SRP492975 PRJNA1083039 SRS20638530 GSM8123101 GSM8123101 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815967 GSM8123102_r1 SRP492975 PRJNA1083039 SRS20638531 GSM8123102 GSM8123102 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815968 GSM8123103_r1 SRP492975 PRJNA1083039 SRS20638532 GSM8123103 GSM8123103 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815969 GSM8123104_r1 SRP492975 PRJNA1083039 SRS20638533 GSM8123104 GSM8123104 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815970 GSM8123105_r1 SRP492975 PRJNA1083039 SRS20638534 GSM8123105 GSM8123105 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815971 GSM8123106_r1 SRP492975 PRJNA1083039 SRS20638535 GSM8123106 GSM8123106 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815972 GSM8123107_r1 SRP492975 PRJNA1083039 SRS20638536 GSM8123107 GSM8123107 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815973 GSM8123108_r1 SRP492975 PRJNA1083039 SRS20638537 GSM8123108 GSM8123108 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815974 GSM8123109_r1 SRP492975 PRJNA1083039 SRS20638538 GSM8123109 GSM8123109 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815975 GSM8123110_r1 SRP492975 PRJNA1083039 SRS20638539 GSM8123110 GSM8123110 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815976 GSM8123111_r1 SRP492975 PRJNA1083039 SRS20638540 GSM8123111 GSM8123111 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION SRX23815977 GSM8123112_r1 SRP492975 PRJNA1083039 SRS20638541 GSM8123112 GSM8123112 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using TRIZOL reagent. Nanopore libraries were prepared according to the direct RNA sequencing protocol from ONT (SQK-RNA002). Because the lengths of poly(A) tails were unknown when we initiated this study, total RNA was used in place of oligo(dT)-selected RNA. Libraries were sequenced on a FLO-MIN106 flow cell and minION sequencing device. Oxford Nanopore Technology direct RNA sequencing MinION