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SRX24179356: RNA-Seq of Cynoglossus semilaevis spleen
1 ILLUMINA (Illumina NovaSeq X) run: 32.2M spots, 8.8G bases, 3Gb downloads

Design: Total RNA of gills were isolated and purified using TRIzol reagent, quantified with NanoDrop ND-1000, and assessed for integrity with Bioanalyzer 2100. Poly(A) RNA was purified from 1g total RNA using Dynabeads Oligo (dT)25-61005, then fragmented with Magnesium RNA Fragmentation Module. Cleaved RNA fragments were reverse-transcribed with SuperScript II Reverse Transcriptase and synthesized into U-labeled second-stranded DNAs with E. coli DNA polymerase I, RNase H, and dUTP Solution. Adapters were ligated to the ends of each strand, followed by size selection with AMPureXP beads. After treatment with heat-labile UDG enzyme, ligated products were PCR amplified, and the final cDNA library had an average insert size of 30050 bp. Finally, paired-end sequencing (PE150) was performed on an Illumina Novaseq X
Submitted by: Qingdao University
Study: Cynoglossus semilaevis Transcriptome or Gene expression
show Abstracthide Abstract
Liver and spleen tissue transcriptome sequencing data from disease-sensitive and disease-tolerant individuals of half-smooth tongue sole (Cynoglossus semilaevis)
Sample: The RNA-seq of spleen tissue in Cynoglossus semilaevis under disease infected
SAMN40861084 • SRS20954162 • All experiments • All runs
Library:
Name: DS-S3
Instrument: Illumina NovaSeq X
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 32.2M spots, 8.8G bases, 3Gb
Run# of Spots# of BasesSizePublished
SRR2857985732,186,6518.8G3Gb2024-04-07

ID:
32490358

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