SRX12674494 YN01 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626070 1YNkm20191201 YN01 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX12674495 YN02 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626071 2YNkm20191202 YN02 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX12674496 YN03 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626072 3YNkm20191203 YN03 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX12674497 YN04 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626073 4YNkm20191204 YN04 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX12674498 YN05 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626074 5YNkm20191205 YN05 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX12674499 YN06 SRP341942 bp0 The RNA samples were processed for Transcriptome sequencing analysis by PTM Biolab Co., Ltd. (Hangzhou, China). A total amount of 3 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer s recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq2500/X platform and 125/150 bp paired-end reads were generated. SRS10626075 6YNkm20191206 YN06 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000