SRX23859741 0D-1 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678871 0D-1 0D-1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859742 0D-2 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678872 0D-2 0D-2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859743 14D-CK-2 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678873 14D-CK-2 14D-CK-2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859744 14D-CK-3 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678874 14D-CK-3 14D-CK-3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859745 14D-UVB-1 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678875 14D-UVB-1 14D-UVB-1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859746 14D-UVB-2 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678876 14D-UVB-2 14D-UVB-2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859747 14D-UVB-3 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678877 14D-UVB-3 14D-UVB-3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859748 0D-3 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678878 0D-3 0D-3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859749 7D-CK-1 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678879 7D-CK-1 7D-CK-1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859750 7D-CK-2 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678880 7D-CK-2 7D-CK-2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859751 7D-CK-3 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678881 7D-CK-3 7D-CK-3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859752 7D-UVB-1 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678882 7D-UVB-1 7D-UVB-1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859753 7D-UVB-2 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678883 7D-UVB-2 7D-UVB-2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859754 7D-UVB-3 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678884 7D-UVB-3 7D-UVB-3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX23859755 14D-CK-1 SRP493762 bp0 mRNA with polyA tail was enriched by Oligo(dT) magnetic beads. Then the RNA was broken into short fragments by fragmentation buffer, and the first cDNA was synthesized with six-base random hexamers based on the fragment RNA template. Then the buffer, dNTPs(dTTP, dATP, dGTP and dCTP) and DNA polymerase I were added to synthesize the double-stranded cDNA, which was then purified by DNA purification magnetic beads. The purified double-stranded cDNA was then end-repaired, A tail was added and a sequencing joint was connected. Then the fragment size was selected by DNA purification magnetic beads, and the final cDNA library was obtained by PCR enrichment. SRS20678885 14D-CK-1 14D-CK-1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000