|
| Status |
Public on Oct 01, 2015 |
| Title |
Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by array
Genome variation profiling by SNP array
SNP genotyping by SNP array
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| |
|
| Citation(s) |
26820068 |
| |
| Submission date |
Sep 18, 2015 |
| Last update date |
Feb 01, 2016 |
| Contact name |
Zirui DONG |
| E-mail(s) |
elvisdong@link.cuhk.edu.hk
|
| Organization name |
The Chinese University of Hong Kong
|
| Department |
Dept. of Obstetrics and Gynaecology
|
| Street address |
Shatin, N.T.
|
| City |
Hong Kong |
| ZIP/Postal code |
999077 |
| Country |
China |
| |
|
| Platforms (4)
|
| GPL8855 |
Illumina HumanCytoSnp-12 Beadchip version 2.0 |
| GPL20897 |
Agilent-022023 Homo sapiens Prenatal Chip V2 [hg19] |
| GPL20898 |
Agilent-035130 Human Fetal Chip V 2.0 [hg19] |
| GPL20899 |
Agilent-068656 human array [hg19] |
|
| Samples (72)
|
|
| This SuperSeries is composed of the following SubSeries: |
| GSE72891 |
aCGH for CNV detection in clinical samples |
| GSE73190 |
Chromosomal microarray analysis for validation of the NGS-based CNV detection results in clinical samples |
|
| Relations |
| BioProject |
PRJNA296348 |
Less...
More...