1644 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by genome tiling array
GSE21541
An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer
45 Raj Chari Dec 31, 2010
GSE38479
Chromosomal copy number aberrations in colorectal metastases resemble their primary counterparts and differences are typically non-recurrent.
130 Daoud Sie Feb 10, 2014
GSE85838
Affymetrix SNP array data for cell line and tumor genotype alignment
15 Elin S. Agoston Aug 31, 2018
GSE103123
Copy number profiling of 556 high-risk neuroblastoma patients using aCGH or SNP arrays
Katleen De Preter Mar 13, 2018
GSE122478
Genome-Wide Detection of CNVs and Their Association with Complex Traits in Holsteins
41 George E Liu Feb 16, 2019
GSE130372
Replication timing alterations in leukemia reflect stable clinically-relevant changes in genome architecture [Repli-Chip]
63 David M Gilbert Dec 27, 2019
GSE8605
Combined arrayCGH and SNP-loss of heterozygosity analysis in cervical cancer
40 Jan Oosting Jul 31, 2007
GSE8627
Genomic integrity of P493 cells
7 Jonathan Pevsner Jul 31, 2007
GSE9609
Phenotypically concordant and discordant monozygotic twins display different DNA copy number variation profiles
58 Jan P Dumanski Dec 11, 2007
GSE10668
The Complete Genome of a Single Individual by Massively Parallel DNA Sequencing
6 Omar Alvi Feb 29, 2008
GSE12751
Evaluation of Wpa-generated amplicons for SNP typing (allele bias), locus bias, and detection of known CNVs
19 Xinghua Pan Sep 24, 2008
GSE13565
Human ES cells reveal recurrent genomic instability at 20q11.21
13 Anselme Louis Perrier Nov 19, 2008
GSE19612
A Hierarchy of Self-Renewing Tumor-Initiating Cell Types in Glioblastoma
171 Anthony Steve Guerrero Apr 22, 2010
GSE20290
Towards a comprehensive structural variation map of an individual human genome for personalized medicine
100 Andy Pang Feb 12, 2013
GSE21991
Myelodysplastic/myeloproliferative neoplasms
156 Andy Chase Jun 30, 2010
GSE25893
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
385 Stephen W Scherer Jun 30, 2011
GSE26233
Genomic profiles vary with race and subtype in young African American and European American breast cancer
98 Theresa V Strong Jan 29, 2013
GSE27367
Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR
375 Tracy Tucker Feb 17, 2011
GSE29211
The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma
131 Yupu Liang May 19, 2011
GSE33483
Mosaic Amplification of Multiple Receptor Tyrosine Kinase Genes in Glioblastoma
3 Matija Snuderl Jan 01, 2012