SRX10332180 GSM5170693 SRP310423 SRS8451894 GSM5170693 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170693 GSM5170693 GEO Accession GSM5170693 SRX10332181 GSM5170694 SRP310423 SRS8451893 GSM5170694 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170694 GSM5170694 GEO Accession GSM5170694 SRX10332182 GSM5170695 SRP310423 SRS8451895 GSM5170695 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170695 GSM5170695 GEO Accession GSM5170695 SRX10332183 GSM5170696 SRP310423 SRS8451896 GSM5170696 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170696 GSM5170696 GEO Accession GSM5170696 SRX10332184 GSM5170697 SRP310423 SRS8451898 GSM5170697 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170697 GSM5170697 GEO Accession GSM5170697 SRX10332185 GSM5170698 SRP310423 SRS8451900 GSM5170698 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170698 GSM5170698 GEO Accession GSM5170698 SRX10332186 GSM5170699 SRP310423 SRS8451897 GSM5170699 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170699 GSM5170699 GEO Accession GSM5170699 SRX10332187 GSM5170700 SRP310423 SRS8451903 GSM5170700 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170700 GSM5170700 GEO Accession GSM5170700 SRX10332188 GSM5170701 SRP310423 SRS8451899 GSM5170701 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170701 GSM5170701 GEO Accession GSM5170701 SRX10332189 GSM5170702 SRP310423 SRS8451901 GSM5170702 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170702 GSM5170702 GEO Accession GSM5170702 SRX10332190 GSM5170703 SRP310423 SRS8451902 GSM5170703 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170703 GSM5170703 GEO Accession GSM5170703 SRX10332191 GSM5170704 SRP310423 SRS8451904 GSM5170704 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170704 GSM5170704 GEO Accession GSM5170704 SRX10332192 GSM5170705 SRP310423 SRS8451905 GSM5170705 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170705 GSM5170705 GEO Accession GSM5170705 SRX10332193 GSM5170706 SRP310423 SRS8451907 GSM5170706 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170706 GSM5170706 GEO Accession GSM5170706 SRX10332194 GSM5170707 SRP310423 SRS8451906 GSM5170707 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170707 GSM5170707 GEO Accession GSM5170707 SRX10332195 GSM5170708 SRP310423 SRS8451909 GSM5170708 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170708 GSM5170708 GEO Accession GSM5170708 SRX10332196 GSM5170709 SRP310423 SRS8451908 GSM5170709 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170709 GSM5170709 GEO Accession GSM5170709 SRX10332197 GSM5170710 SRP310423 SRS8451910 GSM5170710 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170710 GSM5170710 GEO Accession GSM5170710 SRX10332198 GSM5170711 SRP310423 SRS8451911 GSM5170711 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170711 GSM5170711 GEO Accession GSM5170711 SRX10332199 GSM5170712 SRP310423 SRS8451912 GSM5170712 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170712 GSM5170712 GEO Accession GSM5170712 SRX10332200 GSM5170713 SRP310423 SRS8451913 GSM5170713 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170713 GSM5170713 GEO Accession GSM5170713 SRX10332201 GSM5170714 SRP310423 SRS8451914 GSM5170714 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170714 GSM5170714 GEO Accession GSM5170714 SRX10332202 GSM5170715 SRP310423 SRS8451918 GSM5170715 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170715 GSM5170715 GEO Accession GSM5170715 SRX10332203 GSM5170716 SRP310423 SRS8451915 GSM5170716 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170716 GSM5170716 GEO Accession GSM5170716 SRX10332204 GSM5170717 SRP310423 SRS8451916 GSM5170717 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170717 GSM5170717 GEO Accession GSM5170717 SRX10332205 GSM5170718 SRP310423 SRS8451917 GSM5170718 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305170718 GSM5170718 GEO Accession GSM5170718 SRX13351383 GSM5723706 SRP310423 PRJNA714082 SRS11255881 GSM5723706 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723706 GSM5723706 GEO Accession GSM5723706 SRX13351384 GSM5723707 SRP310423 PRJNA714082 SRS11255882 GSM5723707 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723707 GSM5723707 GEO Accession GSM5723707 SRX13351385 GSM5723708 SRP310423 PRJNA714082 SRS11255883 GSM5723708 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723708 GSM5723708 GEO Accession GSM5723708 SRX13351386 GSM5723709 SRP310423 PRJNA714082 SRS11255884 GSM5723709 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723709 GSM5723709 GEO Accession GSM5723709 SRX13351387 GSM5723710 SRP310423 PRJNA714082 SRS11255885 GSM5723710 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723710 GSM5723710 GEO Accession GSM5723710 SRX13351388 GSM5723711 SRP310423 PRJNA714082 SRS11255886 GSM5723711 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723711 GSM5723711 GEO Accession GSM5723711 SRX13351389 GSM5723712 SRP310423 PRJNA714082 SRS11255887 GSM5723712 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723712 GSM5723712 GEO Accession GSM5723712 SRX13351390 GSM5723713 SRP310423 PRJNA714082 SRS11255888 GSM5723713 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723713 GSM5723713 GEO Accession GSM5723713 SRX13351391 GSM5723714 SRP310423 PRJNA714082 SRS11255889 GSM5723714 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted by using the RNeasy Plus Mini Kit (QIAGEN) or NucleoSpin RNA Plus (Takara Bio). RNA was quantified on a NanoDrop 2000c and Qubit. RNA (200 ng) was prepared for library construction. High-quality RNA (RNA Integrity Number value ≥8, as determined by Bioanalyzer) was used for library preparation. RNA-seq libraries were generated using the NEBNext Ultra II Directional RNA Library Prep kit for Illumina (NEB). The number of PCR cycles was minimized to avoid skewing the representation of the libraries. RNA-seq libraries were sequenced on a NextSeq500 (Illumina) as 86 bp single reads. NextSeq 500 gds 305723714 GSM5723714 GEO Accession GSM5723714