SRX5899362 20206-muq_ACTTGA_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820893 20206-muq 20206-muq_ACTTGA_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899363 20206-muq_ACTTGA_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820893 20206-muq 20206-muq_ACTTGA_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899364 20222-gg_GGCTAC_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820892 20222-gg 20222-gg_GGCTAC_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899365 20222-gg_GGCTAC_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820892 20222-gg 20222-gg_GGCTAC_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899366 20222-muq_AGTTCC_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820894 20222-muq 20222-muq_AGTTCC_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899367 20385-gg_TTAGGC_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820895 20385-gg 20385-gg_TTAGGC_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899368 20385-gg_TTAGGC_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820895 20385-gg 20385-gg_TTAGGC_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899369 20285-muq_TGACCA_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820896 20285-muq 20285-muq_TGACCA_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899370 20285-muq_TGACCA_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820896 20285-muq 20285-muq_TGACCA_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899371 20235-muq_TTAGGC_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820897 20235-muq 20235-muq_TTAGGC_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899372 20235-gg_CCGTCC_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820898 20235-gg 20235-gg_CCGTCC_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899373 20235-muq_TTAGGC_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820897 20235-muq 20235-muq_TTAGGC_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899374 20235-gg_CCGTCC_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820898 20235-gg 20235-gg_CCGTCC_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899375 20222-muq_AGTTCC_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820894 20222-muq 20222-muq_AGTTCC_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899376 20243-gg_GCCAAT_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820899 20243-gg 20243-gg_GCCAAT_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899377 20241-gg_AGTCAA_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820900 20241-gg 20241-gg_AGTCAA_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899378 20241-gg_AGTCAA_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820900 20241-gg 20241-gg_AGTCAA_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899379 20241-muq_ATGTCA_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820901 20241-muq 20241-muq_ATGTCA_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899380 20241-muq_ATGTCA_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820901 20241-muq 20241-muq_ATGTCA_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899381 20245-gg_CAGATC_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820902 20245-gg 20245-gg_CAGATC_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899382 20243-muq_CAGATC_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820903 20243-muq 20243-muq_CAGATC_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899383 20243-gg_GCCAAT_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820899 20243-gg 20243-gg_GCCAAT_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899384 20245-gg_CAGATC_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820902 20245-gg 20245-gg_CAGATC_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899385 20243-muq_CAGATC_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820903 20243-muq 20243-muq_CAGATC_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899386 20247-gg_ACTTGA_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820904 20247-gg 20247-gg_ACTTGA_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899387 20247-gg_ACTTGA_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820904 20247-gg 20247-gg_ACTTGA_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899388 20245-muq_GGCTAC_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820905 20245-muq 20245-muq_GGCTAC_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899389 20245-muq_GGCTAC_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820905 20245-muq 20245-muq_GGCTAC_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899390 20247-muq_ATCACG_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820906 20247-muq 20247-muq_ATCACG_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899391 20280-gg_GCCAAT_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820907 20280-gg 20280-gg_GCCAAT_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899392 20275-muq_TGACCA_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820908 20275-muq 20275-muq_TGACCA_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899393 20275-muq_TGACCA_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820908 20275-muq 20275-muq_TGACCA_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899394 20275-gg_TAGCTT_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820909 20275-gg 20275-gg_TAGCTT_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899395 20275-gg_TAGCTT_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820909 20275-gg 20275-gg_TAGCTT_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899396 20247-muq_ATCACG_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820906 20247-muq 20247-muq_ATCACG_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899397 20263-gg_GATCAG_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820910 20263-gg 20263-gg_GATCAG_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899398 20263-gg_GATCAG_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820910 20263-gg 20263-gg_GATCAG_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899399 20263-muq_ACAGTG_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820911 20263-muq 20263-muq_ACAGTG_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899400 20263-muq_ACAGTG_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820911 20263-muq 20263-muq_ACAGTG_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899401 20206-gg_GATCAG_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820912 20206-gg 20206-gg_GATCAG_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899402 20202-muq_ATCACG_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820913 20202-muq 20202-muq_ATCACG_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899403 20202-muq_ATCACG_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820913 20202-muq 20202-muq_ATCACG_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899404 20202-gg_CTTGTA_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820914 20202-gg 20202-gg_CTTGTA_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899405 20206-gg_GATCAG_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820912 20206-gg 20206-gg_GATCAG_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899406 20285-gg_TAGCTT_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820915 20285-gg 20285-gg_TAGCTT_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899407 20285-gg_TAGCTT_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820915 20285-gg 20285-gg_TAGCTT_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899408 20280-muq_CGATGT_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820916 20280-muq 20280-muq_CGATGT_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899409 20280-muq_CGATGT_L004_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820916 20280-muq 20280-muq_CGATGT_L004_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899410 20280-gg_GCCAAT_L005_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820907 20280-gg 20280-gg_GCCAAT_L005_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899411 20196-muq_CGATGT_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820917 20196-muq 20196-muq_CGATGT_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899412 20196-muq_CGATGT_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820917 20196-muq 20196-muq_CGATGT_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899413 20196-gg_ACAGTG_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820918 20196-gg 20196-gg_ACAGTG_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899414 20196-gg_ACAGTG_L002_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820918 20196-gg 20196-gg_ACAGTG_L002_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX5899415 20202-gg_CTTGTA_L001_R1.fastq.gz SRP199490 bp0 poly-A mRNA was purified from 4g of total RNA, fragmented and randomly primed for reverse transcription to generate double stranded cDNA. The cDNA fragments were then subjected to an end repair process, consisting of the addition of a single A base, and the ligation of indexed Illumina adapters at both ends of cDNA. SRS4820914 20202-gg 20202-gg_CTTGTA_L001_R1.fastq.gz RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500