1544 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 SNP array
GSE21349
A compendium of myeloma associated chromosomal copy number abnormalities and their prognostic value
491 Brian A Walker Oct 18, 2010
GSE203509
A comprehensive assessment of a newly designed non-exonic SNP-based NGS panel for HRD detection
  • Genome variation profiling by SNP array
27 Cai Jiang Feb 21, 2023
GSE25893
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
385 Stephen W Scherer Jun 30, 2011
GSE28111
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6)
  • Genome variation profiling by SNP array
36 Stephen W Scherer Jun 30, 2011
GSE28092
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Human1Mv1_C)
36 Stephen W Scherer Jun 30, 2011
GSE28103
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Human660W-Quad)
36 Stephen W Scherer Jun 30, 2011
GSE28104
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (HumanOmni1-Quad)
36 Stephen W Scherer Jun 30, 2011
GSE28101
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (HumanOmni2.5-Quad)
14 Stephen W Scherer Jun 30, 2011
GSE28102
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Illumina_650Y)
18 Stephen W Scherer Jun 30, 2011
GSE28105
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Mapping250K_Nsp)
  • Genome variation profiling by SNP array
14 Stephen W Scherer Jun 30, 2011
GSE71525
A comprehensively characterized cell line panel highly representative of clinical ovarian high-grade serous carcinomas
93 Kelsie L Thu Aug 11, 2016
GSE40142
A framework for identification of actionable cancer genome dependencies in small cell lung cancer
  • Genome variation profiling by SNP array
24 Felix Dietlein Sep 21, 2012
GSE53626
A genetic atlas of human admixture history
158 George Busby Feb 14, 2014
GSE20306
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers
450 Stephen Michael Rothenberg Nov 03, 2011
GSE22284
A genomewide association study for bronchopulmonary dysplasia using DNA pooling
16 Alice Hadchouel Nov 22, 2011
GSE21536
A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33
6 Blake C. Ballif Dec 31, 2010
GSE101551
A humanized mouse model to study type 1 diabetes
  • Genome variation profiling by SNP array
4 Franck Letourneur Jul 19, 2017
GSE151644
A humanized mouse strain that develops spontaneously immune-mediated diabetes.
  • Genome variation profiling by SNP array
5 Franck Letourneur Jun 02, 2021
GSE68794
A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma
2 Esther Korpershoek May 13, 2015
GSE75358
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
36 Raif S. Geha Nov 25, 2015