| Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
|---|---|---|---|---|---|---|---|---|
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Genome variation profiling by SNP array
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TXT
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| GSE162283 |
14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia
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42 | Danika Di Giacomo | Sep 05, 2021 | |||
| GSE13813 |
50K SNP Copy Number Analysis of Ovarian Carcinomas
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118 |
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Dariush Etemadmoghadam | Feb 17, 2009 | ||
| GSE118648 |
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
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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
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172 |
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Muhammad Ghulam Kibriya | Dec 19, 2014 | ||
| GSE30481 |
A Map of Copy Number Variations in Chinese Populations
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155 | Haiyi Lou | Dec 31, 2011 | |||
| GSE7822 |
A comparison of DNA copy number profiling platforms using a panel of melanoma cell lines
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151 |
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Joel Greshock | Nov 02, 2007 | ||
| GSE25893 |
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
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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)
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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)
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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)
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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)
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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)
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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
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24 |
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Felix Dietlein | Sep 21, 2012 | ||
| GSE53626 |
A genetic atlas of human admixture history
|
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158 |
|
George Busby | Feb 14, 2014 | ||
| GSE20306 |
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers
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450 |
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Stephen Michael Rothenberg | Nov 03, 2011 | ||
| GSE22284 |
A genomewide association study for bronchopulmonary dysplasia using DNA pooling
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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
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6 | Blake C. Ballif | Dec 31, 2010 | |||
| GSE68794 |
A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma
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2 |
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Esther Korpershoek | May 13, 2015 | ||
| GSE75314 |
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family A)
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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]
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2 |
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Yuelin Jack Zhu | Dec 22, 2013 |
