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SRX24381196: GSM8239089: N2_emb_RNA_rep1; Caenorhabditis elegans; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 17.4M spots, 889.1M bases, 628.4Mb downloads

External Id: GSM8239089_r1
Submitted by: Ercan, Biology, New York University
Study: mRNA-seq analysis of rex-1 deletion in C. elegans
show Abstracthide Abstract
In embryos, DCC binding across the length of the ~17.7 Mb X chromosome initiates at a set of recruitment elements on the X (rex). Individual rex sites collectively contribute to recruitment and repression, thus deletion of one or few rex sites causes subtle changes, as measured by mRNA-seq in mixed-stage embryos. We previously constructed a strain deleting rex-1, located ~6 kb downstream of dpy-23 (https://doi.org/10.7554/eLife.23645). Here we performed mRNA-seq in rex-1 deletion embryos. Overall design: mRNA-seq in controls and rex-1 deletion embryos.
Sample: N2_emb_RNA_rep1
SAMN41096940 • SRS21137453 • All experiments • All runs
Library:
Name: GSM8239089
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: RNA-seq: Total RNA was purified following Trizol manufacturer's instructions after freeze-cracking samples five times. RNA was cleaned up using Qiagen RNeasy MinElute Cleanup kit. mRNAs were purified using Sera-Mag Oligo (dT) beads (Thermo Scientific) from 10 µg of total RNA. cDNA preparation was done in the presence of dUTP to prepare stranded RNA-seq libraries as in PMID:19620212, cDNA synthesis was performed in the presence of dUTP in order to prepare stranded mRNA-seq libraries. RNA-seq: cDNA was ligated to Illumina adapters and amplified by PCR. Library DNA between 250-500 bp in size was gel purified.
Runs: 1 run, 17.4M spots, 889.1M bases, 628.4Mb
Run# of Spots# of BasesSizePublished
SRR2881812917,433,234889.1M628.4Mb2024-04-29

ID:
32696064

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