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Sample GSM6614315 Query DataSets for GSM6614315
Status Public on May 05, 2024
Title RNAseq_neuron_homo_rep1
Sample type SRA
 
Source name Cultured neurons (2 weeks in vitro) from E18.5 mouse embryo cortex
Organism Mus musculus
Characteristics cell type: Cultured neurons (2 weeks in vitro) from E18.5 mouse embryo cortex
genotype: Ctcf homozygous mutated
strain background: C57BL/6
Treatment protocol CTCF-R567W mutation were generated by CRISPR/Cas9-mediated genome editing.
Growth protocol Mice were housed in a specific pathogen–free (SPF) facility with a 12 h dark/12 h light cycle and provided with food and water ad libitum.
Extracted molecule total RNA
Extraction protocol Total RNAs from each mouse tissue or cells were extracted, and were purified with two rounds of mRNA purification with mRNA capture beads to ensure removal of rRNA.
RNA-seq libraries were constructed using the VAHTS Universal V8 RNA-seq Library Prep Kit for Illumina, and the method was performed according to the manufacturer's instructions.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Description neuron.nor_counts.tsv
Data processing Paired-end reads were handled with Trim Galore, and then mapped to mouse (mm10) or human (hg38) genome using STAR aligner.
Transcript abundance were quantified using RSEM. To remove the effect of gender on gene expression in mouse tissue and neural samples, genes originated from ChrX, ChrY were filtered out. Differentially expressed genes (DEGs) were determined using DESeq2.
Assembly: mm10, hg38
Supplementary files format and content: Tab-delimited text files include normalized count values from DESeq2.
 
Submission date Oct 03, 2022
Last update date May 05, 2024
Contact name gongcheng Hu
Organization name Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences
Street address 190 Kai Yuan Avenue, Science Park, Guangzhou, China
City guangzhou
State/province guangdong
ZIP/Postal code 510530
Country China
 
Platform ID GPL24247
Series (2)
GSE214689 Dissecting developmental disorders caused by CTCF mutation at R567 [RNA-seq]
GSE214692 Dissecting developmental disorders caused by CTCF mutation at R567
Relations
BioSample SAMN31138376
SRA SRX17781635

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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