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Sample GSM7232597 Query DataSets for GSM7232597
Status Public on Apr 27, 2023
Title MGD1551F
Sample type SRA
 
Source name Patient-Derived
Organism Homo sapiens
Characteristics cell line: Patient-Derived
cell type: Fibroblast
genotype: Control
Growth protocol Patient- derived fibroblast cell lines were grown in DMEM (Gibco™, #11-995-073), 10% FBS, 1% Non-essential Amino Acid (100X, Gibco™, 11140-050) and 1% PenStrep at 37℃ in 5% CO2 incubators.
Extracted molecule total RNA
Extraction 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)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Arboleda Lab Pipeline
Samples were demultiplexed after sequencing.
Raw reads were then aligned against the Gencode human genome version hg38 (GR38) version 31 using STAR 2.7.0e with default parameters.
Gene counts from raw reads were generated using featureCounts 1.6.5 from the Subread package. Only reads that uniquely mapped to exons of a gene were counted per gene. Differential expression analysis was completed using DESeq2 v1.24.0, adjusting for sample gender.
Assembly: GR38
Supplementary files format and content: Text files include raw count values for each sample, csv files include DESeq normalized counts per sample
 
Submission date Apr 26, 2023
Last update date Apr 27, 2023
Contact name Valerie Arboleda
E-mail(s) VArboleda@mednet.ucla.edu
Organization name UCLA
Street address 615 Charles E. Young Drive South
City Los Angeles
ZIP/Postal code 90095
Country USA
 
Platform ID GPL24676
Series (2)
GSE230686 Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation [RNA-seq Fibro]
GSE230696 Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation
Relations
BioSample SAMN34386303
SRA SRX20111133

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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