|
| Status |
Public on May 05, 2024 |
| Title |
Dissecting developmental disorders caused by CTCF mutation at R567 |
| Organisms |
Homo sapiens; Mus musculus |
| Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
Other
Expression profiling by high throughput sequencing
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
38951485 |
| |
| Submission date |
Oct 03, 2022 |
| Last update date |
Aug 01, 2024 |
| Contact name |
gongcheng Hu |
| Organization name |
Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences
|
| Street address |
190 Kai Yuan Avenue, Science Park, Guangzhou, China
|
| City |
guangzhou |
| State/province |
guangdong |
| ZIP/Postal code |
510530 |
| Country |
China |
| |
|
| Platforms (4)
|
| GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
| GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
| GPL29480 |
DNBSEQ-T7 (Homo sapiens) |
|
| Samples (71)
|
|
| This SuperSeries is composed of the following SubSeries:
|
| GSE214686 |
Dissecting developmental disorders caused by CTCF mutation at R567 [ChIP-seq] |
| GSE214687 |
Dissecting developmental disorders caused by CTCF mutation at R567 [Hi-C] |
| GSE214688 |
Dissecting developmental disorders caused by CTCF mutation at R567 [4C] |
| GSE214689 |
Dissecting developmental disorders caused by CTCF mutation at R567 [RNA-seq] |
| GSE214690 |
Dissecting developmental disorders caused by CTCF mutation at R567 [snRNA-seq] |
| GSE214691 |
Dissecting developmental disorders caused by CTCF mutation at R567 [SPARC-seq] |
| GSE231847 |
CTCF mutation at R567 causes developmental disorders by 3D genome rearrangement, premature exhaustion of stem cells and abnormal neurodevelopment [scRNA-seq] |
|
| Relations |
| BioProject |
PRJNA886671 |
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