| Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
|---|---|---|---|---|---|---|---|---|
 Filter
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SNP genotyping by SNP array
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Homo sapiens
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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 | |||
| GSE42570 |
5q- Myelodysplastic Syndrome Masquerading as Diamond Blackfan Anemia
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14 |
|
Jason Eli Farrar | Nov 05, 2013 | |
| GSE34678 |
A Genome-wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Possibilities for Future Personalized Treatment
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172 |
|
Muhammad Ghulam Kibriya | Dec 19, 2014 | |
| GSE19612 |
A Hierarchy of Self-Renewing Tumor-Initiating Cell Types in Glioblastoma
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171 |
|
Anthony Steve Guerrero | Apr 22, 2010 | ||
| 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 |
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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)
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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 |
|
Stephen W Scherer | Jun 30, 2011 | |
| 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 |
|
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 | |
| 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 | ||
| GSE75349 |
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family B)
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4 |
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Raif S. Geha | Nov 25, 2015 | |
| GSE48386 |
A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects
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4 |
|
wang liang | Jun 27, 2014 | |
| GSE23785 |
A statistical method for detecting genomic aberrations in heterogeneous tumour samples from single nucleotide polymorphism genotyping data
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9 |
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Christopher Yau | Aug 25, 2010 | |
| GSE141901 |
ASA-750K array genotyping of Northern Han Chinese and Southern Han Chinhttps://www.ncbi.nlm.nih.gov/geo/subsese
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137 |
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Peng Chen | Dec 13, 2019 | |
| GSE23452 |
Acquired Genomic Copy Number Aberrations and Survival in Adult Acute Myelogenous Leukemia
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226 |
|
Sami N Malek | Nov 30, 2010 |
