|
Status |
Public on Aug 10, 2016 |
Title |
HiSeq Chip-seq analysis of whole genomic landscape of G9a and H3K9me2-targeted in CCICs |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Purpose: to demonstrate that G9a maintain CCICs functional triats is independent of its methyltransferase activity. Method: ChIP-seq was applied to CCICs to elucidate the nature of G9a and H3K9me2-regulated differential gene targets by Illumina/Soleza Genome analyzer Results: It was shown that ghe 4,902 G9a-and H3K9me2-targeted genes are broadly idstributed throughout the genome, and both are co-localized at most of the sites in CCICs.
|
|
|
Overall design |
G9a and H3K9me2-targeted in CCICs
|
|
|
Contributor(s) |
Cha S |
Citation missing |
Has this study been published? Please login to update or notify GEO. |
|
Submission date |
Jun 01, 2016 |
Last update date |
May 15, 2019 |
Contact name |
SHIH-TING CHA |
Organization name |
National Taiwan University
|
Street address |
6F., No.2, Syu-jhou Road,
|
City |
TAIPEI |
ZIP/Postal code |
886 |
Country |
Taiwan |
|
|
Platforms (1) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
|
Samples (4)
|
|
Relations |
BioProject |
PRJNA324111 |
SRA |
SRP075976 |