|
Status |
Public on Jan 28, 2019 |
Title |
Genome-wide map of binding sites for HNF4a during hepatic specification of iPS cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
HNF4a has been shown to be critical for hepatocyte differentiation from iPS cells.
|
|
|
Overall design |
Chip-seq was performed on chromatin isolated from iPS cells differentiated to the onset of hepatic specification (day 8).
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|
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Contributor(s) |
Duncan SA, De La Forest A |
Citation(s) |
30597922 |
|
Submission date |
Oct 05, 2017 |
Last update date |
Jul 25, 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) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
|
Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE104779 |
HNF4a Mediated Formation of Hepatic Progenitors |
|
Relations |
BioProject |
PRJNA413299 |
SRA |
SRP119444 |