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SRX5984962: RNA-Seq of octopus vulgaris:paralarva 10 dph
1 ILLUMINA (Illumina HiSeq 4000) run: 56.4M spots, 17G bases, 6.6Gb downloads

Design: Double-stranded cDNA libraries were prepared using the Kapa Stranded mRNA-seq kit (KK8420) following the manufacturer instructions with a mean library insert size of 201300 bp. Briefly, RNA samples were first purified with two oligo-dT selection (poly(A) enrichment using oligodT beds), and then fragmented and reverse transcribed into double-stranded complementary cDNA. A total of 12 libraries were paired-ended sequenced (2 150 bp) in an Illumina HiSeq 4000 platform from individual samples.
Submitted by: IIM-CSIC
Study: RNA sequencing of Octopus vulgaris paralarvae
show Abstracthide Abstract
Rearing Octopus vulgaris under captivity is currently challenged by massive mortalities previous to their juvenile stage due to nutritional and environmental factors. Dissecting the genetic basis and regulatory mechanism behind this mortality requires genomic background knowledge. A transcriptomic sequencing of 10 dph octopus paralarvae from different experimental conditions was constructed via RNA-seq.
Sample:
SAMN11975247 • SRS4890483 • All experiments • All runs
Library:
Name: FZ2_16788_TAGCTT
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 56.4M spots, 17G bases, 6.6Gb
Run# of Spots# of BasesSizePublished
SRR921424556,360,42217G6.6Gb2019-11-19

ID:
8021268

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