GSM7232597: MGD1551F; Homo sapiens; RNA-Seq - SRA

SRX20111133: GSM7232597: MGD1551F; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 49M spots, 11.7G bases, 3.7Gb downloads

External Id: GSM7232597_r1

Submitted by: UCLA

Study: Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation [RNA-seq Fibro]

PRJNA962130 • SRP434720 • All experiments • All runs

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We performed gene expression profiling analysis using data obtained from RNA-seq of BOS patient and control individual fibroblast samples to dissect the transcriptomic effects of truncating ASXL1 mutations. We performed gene expression profiling analysis using data obtained from RNA-seq of BOS patient and control individual fibroblast samples. Overall design: Comparative gene expression profiling analysis of RNA-seq data for Bohring-Opitz syndrome patient blood samples and control blood samples.

Sample: MGD1551F

SAMN34386303 • SRS17441805 • All experiments • All runs

Organism: Homo sapiens

Library:

Name: GSM7232597

Instrument: Illumina NovaSeq 6000

Strategy: RNA-Seq

Source: TRANSCRIPTOMIC

Selection: cDNA

Layout: PAIRED

Construction protocol: RNA was harvested using RNeasy Plus Mini Kit (Qiagen, #74136). 1ug of. NA was used for the construction of sequencing libraries. RNA libraries for RNA-seq were prepared using QIAseq FastSelect −rRNA HMR (Qiagen, #334386) and lllumina Truseq® Stranded Total RNA Library Prep Gold (Illumina, 20020599)

Runs: 1 run, 49M spots, 11.7G bases, 3.7Gb

Run	# of Spots	# of Bases	Size	Published
SRR24316277	48,980,920	11.7G	3.7Gb	2023-04-27

ID:: 27520197

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