708 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 Remove filterTXT
GSE162283
14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia
42 Danika Di Giacomo Sep 05, 2021
GSE13813
50K SNP Copy Number Analysis of Ovarian Carcinomas
  • Genome variation profiling by SNP array
118 Dariush Etemadmoghadam Feb 17, 2009
GSE118648
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
31 Cristina Mecucci Sep 01, 2019
GSE34678
A Genome-wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Possibilities for Future Personalized Treatment
172
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Muhammad Ghulam Kibriya Dec 19, 2014
GSE30481
A Map of Copy Number Variations in Chinese Populations
  • Genome variation profiling by SNP array
155 Haiyi Lou Dec 31, 2011
GSE7822
A comparison of DNA copy number profiling platforms using a panel of melanoma cell lines
151 Joel Greshock Nov 02, 2007
GSE25893
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
385 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
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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
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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
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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
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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
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Stephen W Scherer Jun 30, 2011
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
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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
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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
GSE68794
A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma
2 Esther Korpershoek May 13, 2015
GSE75314
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family A)
32 Raif S. Geha Nov 25, 2015
GSE50136
A novel chordoma xenograft allows in vivo drug testing and reveals the importance of NF-kB signaling in chordoma biology [SNP array]
  • Genome variation profiling by SNP array
2
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Yuelin Jack Zhu Dec 22, 2013