15 series
Export
<<<Page of 1 >>>
Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by SNP array Remove filterPAIR
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
  • Genome variation profiling by SNP array
12
  • Download icon PAIR
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