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SRX2753520: RNAseq of water buffalo mammary carcinoma
1 ILLUMINA (Illumina HiSeq 2500) run: 19.2M spots, 1.9G bases, 828Mb downloads

Design: Illumina HiSeq 2500, Paired end run; 2 X 100 bp. ~5-10 ug of total RNA was used to prepare the RNA seq library using the TruSeq RNA Sample Prep Kits (Illumina). The libraries were prepared as per the kit protocol. Following purification, the mRNA was fragmented into small pieces using divalent cations under elevated temperature. The cleaved mRNA fragments was used to synthesize first strand cDNA synthesis using DNA polymerase I and RNaseH. These cDNA then proceed through an end repair process, the addition of a single 'A' base and ligation of adapters. The prodcuts were purified and enriched with PCR to create the final cDNA library.
Submitted by: Guru Angad Dev Veterinary and Animal Sciences University
Study: Bubalus bubalis Raw sequence reads
show Abstracthide Abstract
Goal of the experiment was to know the gene networks and pathways that are operating in buffalo mammary carcinoma. Rarity of ruminant mammary cacinoma makes this study relevant from agriculture point of view.
Sample: Mammay tissue samples from Bubalus bubalis
SAMN06758773 • SRS2130861 • All experiments • All runs
Organism: Bubalus bubalis
Library:
Name: BUMG_39_2
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: RANDOM PCR
Layout: PAIRED
Runs: 1 run, 19.2M spots, 1.9G bases, 828Mb
Run# of Spots# of BasesSizePublished
SRR546816419,228,9691.9G828Mb2018-09-18

ID:
3970097

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