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Series GSE156020 Query DataSets for GSE156020
Status Public on Jun 07, 2021
Title GATA6 defines endoderm fate by controlling chromatin accessibility during differentiation of human induced pluripotent stem cells [RNA-seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Investigation of the role played by GATA6 in establishing the definitive endoderm chromatin accessbility profile. We used pluripotent stem cells as a model of early development. We derived GATA6-/- pluripotent cells with an inducible GATA6 construct that permits exongenous GATA6 cDNA expression upon supplmentation of doxycycline. We differentiated GATA6 +/+ and GATA6-/- (with and without doxycyline) cells to definitive endoderm and analyzed the gene expression profile by RNA-seq.
 
Overall design Examination of gene expression during definitive endoderm formation in the absence and presence of GATA6.
 
Contributor(s) Heslop JA, Duncan SA
Citation(s) 34010638
Submission date Aug 11, 2020
Last update date Jun 07, 2021
Contact name Stephen A Duncan
E-mail(s) duncanst@musc.edu
Phone 843-792-9104
Organization name Medical University South Carolina
Department Regenerative Medicine and Cell Biology
Lab Duncan Lab
Street address 173 Ashley Avenue, BSB 6th Floor, Room 657A
City Charleston
State/province SC
ZIP/Postal code 29425
Country USA
 
Platforms (1)
GPL23227 BGISEQ-500 (Homo sapiens)
Samples (18)
GSM4720542 RNA - Day 0 - R1 - GATA6+/+
GSM4720543 RNA - Day 0 - R2 - GATA6+/+
GSM4720544 RNA - Day 2 - R1 - GATA6+/+
This SubSeries is part of SuperSeries:
GSE156021 GATA6 defines endoderm fate by controlling chromatin accessibility during differentiation of human induced pluripotent stem cells.
Relations
BioProject PRJNA656447
SRA SRP277025

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
GSE156020_RNA-seq_Normalized_Counts.txt.gz 1.2 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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