| Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
|---|---|---|---|---|---|---|---|---|
 Filter
|
SNP genotyping by SNP array
|
PAIR
|
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| GSE12751 |
Evaluation of Wpa-generated amplicons for SNP typing (allele bias), locus bias, and detection of known CNVs
|
|
19 |
|
Xinghua Pan | Sep 24, 2008 | ||
| GSE20290 |
Towards a comprehensive structural variation map of an individual human genome for personalized medicine
|
|
100 | Andy Pang | Feb 12, 2013 | |||
| GSE25893 |
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
|
|
385 | Stephen W Scherer | Jun 30, 2011 | |||
| GSE27367 |
Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR
|
|
375 | Tracy Tucker | Feb 17, 2011 | |||
| GSE49357 |
De novo copy number variations in cloned dogs
|
|
17 |
|
SeungHyun Jung | Dec 17, 2013 | ||
| GSE79530 |
Characterization of genetic variability of Venezuelan equine encephalitis viruses
|
|
141 |
|
Kevin McLoughlin | Mar 24, 2016 | ||
| GSE87915 |
Individuals with excess numbers of germline de novo CNVs
|
52 | Pengfei Liu | Oct 14, 2016 |
