|
| Status |
Public on Dec 01, 2022 |
| Title |
Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
36493769 |
| |
| Submission date |
Aug 30, 2022 |
| Last update date |
Dec 31, 2022 |
| Contact name |
J. Robert Manak |
| Organization name |
The University of Iowa
|
| Department |
Biology and Pediatrics
|
| Lab |
Manak Lab
|
| Street address |
455 Biology Building, 129 East Jefferson Street
|
| City |
Iowa City |
| State/province |
Iowa |
| ZIP/Postal code |
52242 |
| Country |
USA |
| |
|
| Platforms (2) |
| GPL8736 |
Agilent-021529 Human CGH Whole Genome Microarray 1x1M (G4447A) (Feature Number version) |
| GPL23665 |
NimbleGen Human CGH 2.1M Whole-Genome Tiling Array [100718_HG18_WG_CGH_v2D_HX1] |
|
| Samples (1108)
|
|
| This SuperSeries is composed of the following SubSeries: |
| GSE212165 |
CNV analysis of 233 individuals of European ancestry and 6 individuals of non-European ancestry with cleft lip and/or cleft palate |
| GSE212166 |
CNV analysis of 869 individuals from the Philippines with cleft lip and/or cleft palate |
|
| Relations |
| BioProject |
PRJNA874904 |
Less...
More...