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SRX713887: Carcinus maenas transcriptome - gill
1 ILLUMINA (Illumina HiSeq 2500) run: 10.1M spots, 2G bases, 1.3Gb downloads

Design: RNA was extracted using Qiagen’s miRNeasy mini kit as per manufacturer’s instructions, with on column DNase digestion. RNA quality and integrity was checked, and quantity measured using Agilent Bioanalyser. cDNA libraries for each tissue were constructed using equal amounts of RNA from four individuals that were pooled together. ERCC Spike-In control mixes were added to control for technical variation during sample preparation and sequencing. mRNA purification was performed via poly(A) enrichment using Tru-Seq low throughput protocol and reagents (Illumina) and finally cDNA libraries constructed using Epicentre’s ScriptSeq v2 RNA-seq library preparation kit.
Submitted by: University of Exeter
Study: Carcinus maenas Transcriptome
show Abstracthide Abstract
RNA was isolated from 12 tissues of 4 Carcinus maenas individuals. For every tissue the RNA from each individual was pooled. The RNA was sequenced on an Illumina HiSeq 2500 sequencing machine (Exeter sequencing service: http://ess-wiki.exeter.ac.uk/ess/Exeter_Sequencing_Service). After quality control the RNA was used to produce a de novo assembled transcriptome. The transcriptome was annotated through sequence similarity searches to the NCBI databases. The immune pathways were characterized in detail to provide a basis for further studies.
Sample: GLL01
SAMN03016050 • SRS711835 • All experiments • All runs
Organism: Carcinus maenas
Library:
Name: Cmaenas_gill
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Spot descriptor:
forward101  reverse

Runs: 1 run, 10.1M spots, 2G bases, 1.3Gb
Run# of Spots# of BasesSizePublished
SRR158961710,110,1022G1.3Gb2015-09-29

ID:
1005215

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