131 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
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GSE21168
Gene amplification of the transcription factor DP1 and the CTNND1 in human lung cancer
4 Sandra Castillo Apr 11, 2010
GSE21097
Acquired chromosome abnormalities in the lungs of patients with Pulmonary Arterial Hypertension (Illumina)
24 Christopher D Coldren May 01, 2010
GSE21541
An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer
45 Raj Chari Dec 31, 2010
GSE53261
The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts
304 Stephan Busche Dec 13, 2013
GSE61129
Exonic variants associated with development of Aspirin Exacerbated Respiratory Diseases
  • SNP genotyping by SNP array
969
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Seung-Woo Shin Sep 05, 2014
GSE66677
Effective population size, extended linkage disequilibrium and signatures of selection in the rare dog breed Lundehund
28 Ottmar Distl Mar 09, 2015
GSE67618
Map the causative gene of hearing loss in Chinese Rongchang pigs by GWAS
101
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Ting huan zhang May 01, 2015
GSE68794
A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma
2 Esther Korpershoek May 13, 2015
GSE66747
Copy number variation of human intestinal stem cells with different passage in culture (two pedigrees, passage 5, 10, 15 and 20)
9 Frank McKeon May 29, 2015
GSE66748
Copy number variation of human intestinal stem cells with different passage in culture (five pedifrees, passage 5 and 25)
11 Frank McKeon May 29, 2015
GSE66749
Cloning and Variation of Ground State Intestinal Stem Cells Super [expression & SNP studies]
66 Frank McKeon May 29, 2015
GSE64572
The UBC-40 Urothelial Bladder Cancer Cell Line Index [copy number variation]
50 Enrique Carrillo de Santa Pau Jun 19, 2015
GSE64573
The UBC-40 Urothelial Bladder Cancer Cell Line Index
70 Enrique Carrillo de Santa Pau Jun 19, 2015
GSE73190
Chromosomal microarray analysis for validation of the NGS-based CNV detection results in clinical samples
53 Zirui DONG Oct 01, 2015
GSE73191
Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples
72 Zirui DONG Oct 01, 2015
GSE68662
Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.0 Beadchip)
8 Frank McKeon Jan 13, 2016
GSE68663
Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.1 Beadchip)
53 Frank McKeon Jan 13, 2016
GSE68664
Copy number variation analysis of human Barrett's esophagus stem cells
61
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Frank McKeon Jan 13, 2016
GSE71429
Infinium 850k Beadchip analysis of control human brain for copy number mosaicism
  • SNP genotyping by SNP array
7 Christos Proukakis Feb 01, 2016
GSE71470
Modifying DNA extraction protocol alters human brain copy number estimation
40 Christos Proukakis Feb 01, 2016