SRX2925315 GSM2671530 SRP109545 SRS2290587 GSM2671530 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671530 GSM2671530 GEO Accession GSM2671530 SRX2925317 GSM2671531 SRP109545 SRS2290588 GSM2671531 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671531 GSM2671531 GEO Accession GSM2671531 SRX2925318 GSM2671532 SRP109545 SRS2290589 GSM2671532 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671532 GSM2671532 GEO Accession GSM2671532 SRX2925319 GSM2671533 SRP109545 SRS2290591 GSM2671533 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671533 GSM2671533 GEO Accession GSM2671533 SRX2925320 GSM2671534 SRP109545 SRS2290590 GSM2671534 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671534 GSM2671534 GEO Accession GSM2671534 SRX2925321 GSM2671535 SRP109545 SRS2290592 GSM2671535 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671535 GSM2671535 GEO Accession GSM2671535 SRX2925322 GSM2671536 SRP109545 SRS2290593 GSM2671536 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671536 GSM2671536 GEO Accession GSM2671536 SRX2925323 GSM2671537 SRP109545 SRS2290595 GSM2671537 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671537 GSM2671537 GEO Accession GSM2671537 SRX2925324 GSM2671538 SRP109545 SRS2290594 GSM2671538 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671538 GSM2671538 GEO Accession GSM2671538 SRX2925325 GSM2671539 SRP109545 SRS2290596 GSM2671539 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671539 GSM2671539 GEO Accession GSM2671539 SRX2925326 GSM2671540 SRP109545 SRS2290597 GSM2671540 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671540 GSM2671540 GEO Accession GSM2671540 SRX2925327 GSM2671541 SRP109545 SRS2290598 GSM2671541 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671541 GSM2671541 GEO Accession GSM2671541 SRX2925328 GSM2671542 SRP109545 SRS2290599 GSM2671542 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671542 GSM2671542 GEO Accession GSM2671542 SRX2925329 GSM2671543 SRP109545 SRS2290600 GSM2671543 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671543 GSM2671543 GEO Accession GSM2671543 SRX2925330 GSM2671544 SRP109545 SRS2290601 GSM2671544 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671544 GSM2671544 GEO Accession GSM2671544 SRX2925331 GSM2671545 SRP109545 SRS2290602 GSM2671545 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671545 GSM2671545 GEO Accession GSM2671545 SRX2925332 GSM2671546 SRP109545 SRS2290603 GSM2671546 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671546 GSM2671546 GEO Accession GSM2671546 SRX2925333 GSM2671547 SRP109545 SRS2290604 GSM2671547 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671547 GSM2671547 GEO Accession GSM2671547 SRX2925334 GSM2671548 SRP109545 SRS2290605 GSM2671548 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671548 GSM2671548 GEO Accession GSM2671548 SRX2925335 GSM2671549 SRP109545 SRS2290606 GSM2671549 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671549 GSM2671549 GEO Accession GSM2671549 SRX2925336 GSM2671550 SRP109545 SRS2290608 GSM2671550 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671550 GSM2671550 GEO Accession GSM2671550 SRX2925337 GSM2671551 SRP109545 SRS2290607 GSM2671551 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671551 GSM2671551 GEO Accession GSM2671551 SRX2925338 GSM2671552 SRP109545 SRS2290609 GSM2671552 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671552 GSM2671552 GEO Accession GSM2671552 SRX2925339 GSM2671553 SRP109545 SRS2290610 GSM2671553 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671553 GSM2671553 GEO Accession GSM2671553 SRX2925340 GSM2671554 SRP109545 SRS2290611 GSM2671554 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671554 GSM2671554 GEO Accession GSM2671554 SRX2925341 GSM2671555 SRP109545 SRS2290612 GSM2671555 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671555 GSM2671555 GEO Accession GSM2671555 SRX2925342 GSM2671556 SRP109545 SRS2290613 GSM2671556 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671556 GSM2671556 GEO Accession GSM2671556 SRX2925343 GSM2671557 SRP109545 SRS2290615 GSM2671557 RNA-Seq TRANSCRIPTOMIC cDNA Leaf tissue was ground to a fine powder in liquid nitrogen. Total RNA was prepared using the DirectZol RNA extraction kit (Zymo Research). Quality of the RNA extractions was assessed using a Bioanalyzer (Aligent). The libraries were prepared at the University of Utah High Throughput Genomics facility using the Illumina TruSeq Stranded mRNA Library Preparation Kit with poly(A) selection. Illumina HiSeq 2500 gds 302671557 GSM2671557 GEO Accession GSM2671557