|
| Status |
Public on Mar 21, 2018 |
| Title |
CytoScan HD array data for a patient with Vitamin D deficiency |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
Genome variation profiling by SNP array
|
| Summary |
Chromosome microarray (CMA) was performed to identify a possible CNV or ROH that could be contributing to this patient's clinical phenotype.
|
| |
|
| Overall design |
CytoScan HD arrays were performed according to the manufacturer's directions on DNA extracted from a blood sample. Copy number and ROH analysis was performed using the ChAS software.
|
| |
|
| Contributor(s) |
Brown L, Marcadier J |
| Citation(s) |
30893535 |
| Submission date |
Mar 20, 2018 |
| Last update date |
Mar 02, 2021 |
| Contact name |
Lindsay Brown |
| E-mail(s) |
lbrown5@cw.bc.ca
|
| Organization name |
BC Children's and Woman's Health Centre of BC
|
| Street address |
4480 Oak St
|
| City |
Vancouver |
| ZIP/Postal code |
V6H 3N1 |
| Country |
Canada |
| |
|
| Platforms (1) |
| GPL16131 |
[CytoScanHD_Array] Affymetrix CytoScan HD Array |
|
| Samples (1) |
|
| Relations |
| BioProject |
PRJNA439315 |
