|
Status |
Public on Sep 23, 2021 |
Title |
Hepatitis C virus scarring of the epigenome and creates targetable vulnerabilities following viral clearance |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing Methylation profiling by genome tiling array
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation(s) |
34387871 |
Submission date |
Mar 03, 2021 |
Last update date |
Dec 23, 2021 |
Contact name |
Keith D Robertson |
E-mail(s) |
robertson.keith@mayo.edu
|
Phone |
507-266-4886
|
Organization name |
Mayo Clinic
|
Department |
Molecular Pharmacology & Experimental Therapeutics
|
Lab |
Epigenetic Etiology of Human Disease Laboratory
|
Street address |
200 First Street SW, Stabile 12-70
|
City |
Rochester |
State/province |
MN |
ZIP/Postal code |
55905 |
Country |
USA |
|
|
Platforms (3) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
GPL21145 |
Infinium MethylationEPIC |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
|
Samples (83)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE168178 |
Clearance of chronic hepatitis C virus infection leaves scars on the epigenome driven by an interferon response and creates targetable vulnerabilities [seq] |
GSE168185 |
Interferon drives hepatitis C virus scarring of the epigenome and creates targetable vulnerabilities following viral clearance [array] |
|
Relations |
BioProject |
PRJNA706410 |