SRX18550296 GSM6807305_r1 SRP412194 PRJNA910520 SRS16016727 GSM6807305 GSM6807305 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550297 GSM6807306_r1 SRP412194 PRJNA910520 SRS16016726 GSM6807306 GSM6807306 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550298 GSM6807307_r1 SRP412194 PRJNA910520 SRS16016728 GSM6807307 GSM6807307 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550299 GSM6807308_r1 SRP412194 PRJNA910520 SRS16016729 GSM6807308 GSM6807308 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550300 GSM6807309_r1 SRP412194 PRJNA910520 SRS16016730 GSM6807309 GSM6807309 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550301 GSM6807310_r1 SRP412194 PRJNA910520 SRS16016731 GSM6807310 GSM6807310 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550302 GSM6807311_r1 SRP412194 PRJNA910520 SRS16016732 GSM6807311 GSM6807311 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550303 GSM6807312_r1 SRP412194 PRJNA910520 SRS16016733 GSM6807312 GSM6807312 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000 SRX18550304 GSM6807313_r1 SRP412194 PRJNA910520 SRS16016734 GSM6807313 GSM6807313 RNA-Seq TRANSCRIPTOMIC cDNA The cells were lysed with Trizol to obtain total RNA and verification for purity and integrity of total RNA was conducted RNA libraries for RNA-seq were prepared using SMARTER mRNA-Seq Library Prep Kit following manufacturer's protocols. Sample RNA was segmented, the segmented RNA was reverse-transcribed to generate double-stranded DNA, and the double-stranded DNA ends were processed for PCR amplification. The products amplified by PCR were terminologically denatured to form single strands, which were cycled and a single strand circular DNA library was established. High-throughput transcriptome sequencing was performed with Illumina Nova6000 sequencing platform for the DNA library, and the original data of transcriptome sequencing was finally obtained. Illumina NovaSeq 6000