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Series GSE108275 Query DataSets for GSE108275
Status Public on Mar 28, 2018
Title Analysis of gene expression profile in the control and CHD7-knockdown hiPSC-derived lt-NES cells (scRNA-Seq)
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary CHARGE syndrome is a congenital disorder caused by mutations in Chromodomain Helicase DNA-binding domain 7 (CHD7) gene. We performed single cell RNA-seq analysis in CTRL and CHD7-knockdown lt-NES cells.
 
Overall design Single cell RNA-Seq profiling of control (shCTRL) and CHD7-knockdown (sh410 or sh411) cells.
 
Citation(s) 29440260
Submission date Dec 19, 2017
Last update date Mar 27, 2019
Contact name Tsukasa Sanosaka
E-mail(s) sanosaka@keio.jp
Organization name Keio University School of Medicine
Department Department of Physiology
Street address 35 Shinanomachi
City Shinjuku-ku
State/province Tokyo
ZIP/Postal code 1608582
Country Japan
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (92)
GSM2894227 CTRL_A01
GSM2894228 CTRL_A02
GSM2894229 CTRL_A03
This SubSeries is part of SuperSeries:
GSE111327 Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors
Relations
BioProject PRJNA423024
SRA SRP127035

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE108275_SF_Gene_TPM_matrix.txt.gz 3.3 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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