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SRX9152880: RNAseq of female Lymantria dispar dispar pupa, CT strain, day 3
1 ION_TORRENT (Ion Torrent Proton) run: 11.6M spots, 1.4G bases, 1Gb downloads

Design: Samples were homogenized in Trizol reagent (Ambion, Life Technologies; 4 to 7 mL depending on the size of the pupa) using 15 mL disposable tissue grinders (VWR, Cat.47732-446). For each sample, 500 L of the homogenate was transferred to a 1.5 mL microfuge tube, to which another 500 L of Trizol was added. The tubes were then centrifuged for 4 min at 17,000 x g to pellet debris. 400 L of the supernatant was subsequently used for RNA extraction using the Direct-zol RNA miniprep kit (Zymo Research). RNA was eluted using 50 L of water, quantified using a NanoDrop ND1000 spectrophotometer (Thermo Fisher Scientific Inc.), and assessed for quality using a 2100 Bioanalyzer system (Agilent). RNASeq libraries and Ion Proton sequencing were performed at the Genomic Analysis Platform of the Institute of Integrative and Systems Biology (Laval University, Quebec, QC, Canada) using the NEBNext Ultra II directional RNA library prep kit (New England BioLabs) with the NEBNext Poly (A) mRNA magnetic isolation module. Ion Proton sequencing was performed on an Ion Chef with a P1 chip according to manufacturer's instructions.
Submitted by: Natural Resources Canada
Study: Gypsy moth gene expression during female pupal development
show Abstracthide Abstract
This project aims to compare the gene expression of female pupae from Asian (flight capable) and European (flight incapable) populations.
Sample: Gypsy Moth Strain CT, Day 3, Replicate 3
SAMN16213545 • SRS7392856 • All experiments • All runs
Library:
Name: Cusson_F1
Instrument: Ion Torrent Proton
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: Oligo-dT
Layout: SINGLE
Runs: 1 run, 11.6M spots, 1.4G bases, 1Gb
Run# of Spots# of BasesSizePublished
SRR1267268811,579,9331.4G1Gb2024-06-06

ID:
11925464

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