RNA-seq of sus scrofa young male jejunum

SRX3403495 A1 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 A1 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500 SRX3403496 C3 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 C3 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500 SRX3403497 C2 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 C2 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500 SRX3403498 C1 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 C1 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500 SRX3403499 A3 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 A3 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500 SRX3403500 A2 RNA-seq of sus scrofa young male jejunum SRP125181 PRJNA418680 The jejunum tissues were completely grounded in liquid nitrogen and total RNA was extracted using the Trizol reagent according to manufacturer s instructions (Invitrogen). An additional DNase I digestion step was performed to ensure that the samples were not contaminated with genomic DNA. The quality of the total RNA was checked using the the Nanodrop-2000. Each RNA sample had an A260:A280 ratio above 1.8 and an A260:A230 ratio above 2.2. A total amount of 10 g RNA per sample was used as input material for the mRNA sample preparations. Libraries were prepared according to the manufacturer's instructions and sequenced using an Illumina HiSeqTM 2500 platform. SRS2697379 SAMN08031334 A2 RNA-Seq TRANSCRIPTOMIC size fractionation Illumina HiSeq 2500