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SRX8753452: RNA-Seq of B.pyrosoma
1 ILLUMINA (Illumina HiSeq 2500) run: 88.5M spots, 26.5G bases, 8Gb downloads

Design: Each sample was separated to extract RNA using TRIzol Reagent (Life Technologies, USA). RNA degradation and contamination were monitored on 1% agarose gels. RNA purity was checked using the NanoPhotometer spectrophotometer (IMPLEN, CA, USA). RNA integrity was assessed using the RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). A total amount of 1.5 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext Ultra RNA Library Prep Kit for Illumina (NEB, USA) following manufacturers recommendations and index codes were added to attribute sequences to each sample. The clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumia) according to the manufacturers instructions.
Submitted by: Institute of Apicultural Research, Chinese Academy of Agricultural Sciences
Study: B. pyrosoma RNA-Seq
show Abstracthide Abstract
Comparative transcriptome reveals the adaptation mechanism of B.pyrosoma inhabiting on Tibet Plateau
Sample:
SAMN15566564 • SRS7025469 • All experiments • All runs
Organism: Bombus pyrosoma
Library:
Name: Lg3
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: RT-PCR
Layout: PAIRED
Runs: 1 run, 88.5M spots, 26.5G bases, 8Gb
Run# of Spots# of BasesSizePublished
SRR1224552388,469,97526.5G8Gb2021-02-08

ID:
11384707

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