|
| Status |
Public on Nov 08, 2013 |
| Title |
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
24127591 |
| Submission date |
Sep 30, 2013 |
| Last update date |
May 15, 2019 |
| Contact name |
Francis S Collins |
| E-mail(s) |
collinsf@mail.nih.gov
|
| Organization name |
NHGRI
|
| Department |
Genome Technology Branch
|
| Lab |
Molecular Genetics Section
|
| Street address |
1 Center Drive, Rm 126
|
| City |
Bethesda |
| State/province |
MD |
| ZIP/Postal code |
20892 |
| Country |
USA |
| |
|
| Platforms (2) |
| GPL9115 |
Illumina Genome Analyzer II (Homo sapiens) |
| GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
|
| Samples (13)
|
|
| This SuperSeries is composed of the following SubSeries: |
| GSE51310 |
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants (RNA-seq) |
| GSE51311 |
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants (ChIP-seq) |
|
| Relations |
| BioProject |
PRJNA227207 |
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