SRX10410769 GSM5195902 SRP311653 SRS8532380 GSM5195902 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195902 GSM5195902 GEO Accession GSM5195902 SRX10410770 GSM5195903 SRP311653 SRS8532381 GSM5195903 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195903 GSM5195903 GEO Accession GSM5195903 SRX10410771 GSM5195904 SRP311653 SRS8532382 GSM5195904 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195904 GSM5195904 GEO Accession GSM5195904 SRX10410772 GSM5195905 SRP311653 SRS8532383 GSM5195905 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195905 GSM5195905 GEO Accession GSM5195905 SRX10410773 GSM5195906 SRP311653 SRS8532384 GSM5195906 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195906 GSM5195906 GEO Accession GSM5195906 SRX10410774 GSM5195907 SRP311653 SRS8532385 GSM5195907 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195907 GSM5195907 GEO Accession GSM5195907 SRX10410775 GSM5195908 SRP311653 SRS8532386 GSM5195908 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195908 GSM5195908 GEO Accession GSM5195908 SRX10410776 GSM5195909 SRP311653 SRS8532387 GSM5195909 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195909 GSM5195909 GEO Accession GSM5195909 SRX10410777 GSM5195910 SRP311653 SRS8532388 GSM5195910 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195910 GSM5195910 GEO Accession GSM5195910 SRX10410778 GSM5195911 SRP311653 SRS8532389 GSM5195911 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195911 GSM5195911 GEO Accession GSM5195911 SRX10410779 GSM5195912 SRP311653 SRS8532390 GSM5195912 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195912 GSM5195912 GEO Accession GSM5195912 SRX10410780 GSM5195913 SRP311653 SRS8532391 GSM5195913 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195913 GSM5195913 GEO Accession GSM5195913 SRX10410781 GSM5195914 SRP311653 SRS8532392 GSM5195914 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195914 GSM5195914 GEO Accession GSM5195914 SRX10410782 GSM5195915 SRP311653 SRS8532393 GSM5195915 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195915 GSM5195915 GEO Accession GSM5195915 SRX10410783 GSM5195916 SRP311653 SRS8532394 GSM5195916 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195916 GSM5195916 GEO Accession GSM5195916 SRX10410784 GSM5195917 SRP311653 SRS8532395 GSM5195917 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195917 GSM5195917 GEO Accession GSM5195917 SRX10410785 GSM5195918 SRP311653 SRS8532396 GSM5195918 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195918 GSM5195918 GEO Accession GSM5195918 SRX10410786 GSM5195919 SRP311653 SRS8532397 GSM5195919 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195919 GSM5195919 GEO Accession GSM5195919 SRX10410787 GSM5195920 SRP311653 SRS8532398 GSM5195920 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195920 GSM5195920 GEO Accession GSM5195920 SRX10410788 GSM5195921 SRP311653 SRS8532399 GSM5195921 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195921 GSM5195921 GEO Accession GSM5195921 SRX10410789 GSM5195922 SRP311653 SRS8532400 GSM5195922 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195922 GSM5195922 GEO Accession GSM5195922 SRX10410790 GSM5195923 SRP311653 SRS8532401 GSM5195923 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195923 GSM5195923 GEO Accession GSM5195923 SRX10410791 GSM5195924 SRP311653 SRS8532402 GSM5195924 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195924 GSM5195924 GEO Accession GSM5195924 SRX10410792 GSM5195925 SRP311653 SRS8532403 GSM5195925 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the Qiagen RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Samples were Turbo DNase (Thermo Fisher Scientific, Waltham, MA, USA) treated, and RNA quantity and quality was assessed using an Agilent 4200 TapeStation (Agilent Technologies Inc., Santa Clara, CA). Libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation Kit and approximately 30,000,000 50nt single-end Illumina reads were generated for each sample on the Illumina HiSeq 4000 platform. Illumina HiSeq 4000 gds 305195925 GSM5195925 GEO Accession GSM5195925