Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
---|---|---|---|---|---|---|---|---|
Filter | Genome variation profiling by SNP array | PAIR | ||||||
GSE16400 |
The pitfalls of platform comparison: DNA copy number array technologies assessed
|
|
179 | Christina Curtis | Dec 03, 2009 | |||
GSE31575 |
Ribosomal Protein Gene Deletions in Diamond Blackfan Anemia
|
|
74 |
|
Jason Eli Farrar | Jan 15, 2012 | ||
GSE76560 |
Transcriptome profiling in five vitally important tissues of Cynomolgus monkeys using customized NimbleGen microarrays
|
|
105 |
|
Tobias Heckel | Feb 24, 2016 | ||
GSE76708 |
Diversity and regulatory impact of copy number variation in the primate Macaca fascicularis
|
|
126 | Tobias Heckel | Feb 24, 2016 | |||
GSE64122 |
Detection of copy number variation in patients with Pelizaeus-Merzbacher disease (PMD)
|
|
14 | Grace Hobson | Feb 09, 2015 | |||
GSE33987 |
Progression of Neuroblastoma Tumor
|
|
3 |
|
Peter Johansson | Dec 01, 2011 | ||
GSE60259 |
DNA copy number detection from exome sequencing - Exploiting the off-targets
|
|
10 |
|
Oscar Krijgsman | Aug 12, 2014 | ||
GSE46848 |
The distribution of genomic variations in human iPSCs is related to replication timing reorganization during reprogramming
|
|
17 | Hu Li | Mar 28, 2014 | |||
GSE87915 |
Individuals with excess numbers of germline de novo CNVs
|
|
52 | Pengfei Liu | Oct 14, 2016 | |||
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 | |||
GSE56521 |
Sex-specific gene expression profiles of Aedes aegypti 24 hr pupal heads
|
|
12 | Molly Duman Scheel | Oct 27, 2014 | |||
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 | |||
GSE85010 |
Rare germline copy number variations and disease susceptibility in familial melanoma
|
|
254 |
|
Rose Yang | Dec 01, 2016 |