U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

SRX6433805: RNA-Seq of Sillago sihama: hypoxia 1h-treated fish gill bioreplicate 3
1 ILLUMINA (Illumina HiSeq 2500) run: 24M spots, 7.2G bases, 2.2Gb downloads

Design: Fragmentation was carried out using divalent cations under elevated temperature in NEBNext First Strand Synthesis Reaction Buffer(5X). First strand cDNA was synthesized using random hexamer primer and M-MuLV Leading Edge Genomic Services & Solutions Reverse Transcriptase(RNase H - ). Second strand cDNA synthesis was subsequently performed using DNA Polymerase I and RNase H. Remaining overhangs were converted into blunt ends via exonuclease/polymerase activities. After adenylation of 3 ends of DNA fragments, NEBNext Adaptor with hairpin loop structure were ligated to prepare for hybridization. In order to select cDNA fragments of preferentially 250~300 bp in length, the library fragments were purified with AMPure XP system
Submitted by: Guangdong Ocean University
Study: raw transcriptome sequence data of sillago sihama: hypoxia fish gill
show Abstracthide Abstract
Compared the transcriptome data of the hypoxic treatment group and the normal group to search hypoxia-related genes.
Sample:
SAMN12257700 • SRS5088409 • All experiments • All runs
Organism: Sillago sihama
Library:
Name: HI_G_3
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 24M spots, 7.2G bases, 2.2Gb
Run# of Spots# of BasesSizePublished
SRR967334624,040,1347.2G2.2Gb2020-08-09

ID:
8523956

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...