|
Status |
Public on Oct 01, 2015 |
Title |
AF [12ZS032519] |
Sample type |
genomic |
|
|
Source name |
Prenatal diagnosis_AF
|
Organism |
Homo sapiens |
Characteristics |
sample origin: Prenatal diagnosis clinical indication: adv mat age tissue: Amniotic fluid
|
Treatment protocol |
Samples were untreated
|
Growth protocol |
Uncultured samples of chorionic villus sampling, amniotic fluid, placental tissue and blood were used for direct DNA extraction
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA extraction done by Qiagen DNeasy® Blood & Tissue Kit following manufacturer's instructions
|
Label |
C-Bio and A-DNP
|
Label protocol |
Illumina standard protocol for CytoSNP 12 chips (GPL16483), using automation with the Tecan Evo robot.
|
|
|
Hybridization protocol |
Illumina standard protocol for CytoSNP 12 chips (GPL16483), using automation with the Tecan Evo robot.
|
Scan protocol |
Illumina standard protocol for CytoSNP 12 chips (GPL16483), using automation with the Tecan Evo robot.
|
Data processing |
Genomic DNA was genotyped using KaryoStudio V 1.3.11 and GenomeStudio V2011.1 (Illumina) based on hg19.
|
|
|
Submission date |
Sep 18, 2015 |
Last update date |
Oct 01, 2015 |
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 |
|
|
Platform ID |
GPL8855 |
Series (2) |
GSE73190 |
Chromosomal microarray analysis for validation of the NGS-based CNV detection results in clinical samples |
GSE73191 |
Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples |
|