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SRX24839475: GSM8313939: X1i; Rattus norvegicus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 65.4M spots, 13.2G bases, 3.8Gb downloads

External Id: GSM8313939_r1
Submitted by: Day, Neurobiology, UAB
Study: RNA-seq dataset for "Reelin marks cocaine-activated striatal ensembles, promotes neuronal excitability, and regulates cocaine reward"
show Abstracthide Abstract
This dataset contains RNA-seq results from rat embryonic striatal neuronal cultures treated with CRISPRi machinery (dCas9-KRAB-MeCP2 fusion) with a CRISPR sgRNA targeting lacZ (a bacterial gene not found in the mammalian genome; used as a non-targeting control) or Reln. Overall design: This experiment contains 8 biological samples, each of which underwent RNA-seq on an Illumina NovaSeq6000 instrument. Samples were treated with CRISPRi machinery targeting lacZ (lacZ control; samples X1i, X2i, X3i, X4i), or Reln (samples X5i, X6i, X7i, X8i) . Forward and reverse paired-end reads are denoted as "R1" or "R2" in raw file names.
Sample: X1i
SAMN41748868 • SRS21551028 • All experiments • All runs
Library:
Name: GSM8313939
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA from was extracted, DNase-treated, and purified (RNeasy, Qiagen). 1µg of total RNA underwent quality control (Bioanalyzer; all RIN values > 7.0) and library construction for polyA+ RNA sequencing. 1 μg of total RNA underwent quality control (Bioanalyzer) and was prepared for directional RNA sequencing using NEBNext reagents (New England Biolabs) according to manufacturer's recommendations. Specifically, the NEBNext Poly(A) mRNA manetic isolation module was used to enrich polyadenylated RNA. RNA-seq libraries underwent sequencing (100 bp paired-end directional reads) on an Illumina sequencing platform (NovaSeq6000).
Runs: 1 run, 65.4M spots, 13.2G bases, 3.8Gb
Run# of Spots# of BasesSizePublished
SRR2932302465,382,20813.2G3.8Gb2024-07-10

ID:
33173809

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