Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
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GSE169469 |
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
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2 | Xuejiao Chen | Mar 24, 2021 | |||
GSE162283 |
14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia
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42 | Danika Di Giacomo | Sep 05, 2021 | |||
GSE20368 |
1q gain clinical impact in Ewing's Sarcoma: role of DTL
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94 | Carlos Mackintosh | Aug 01, 2011 | |||
GSE53021 |
250K SNP array data for 40 high-grade myogenic cancers
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47 | Jonathan A Fletcher | May 02, 2014 | |||
GSE13813 |
50K SNP Copy Number Analysis of Ovarian Carcinomas
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118 | Dariush Etemadmoghadam | Feb 17, 2009 | |||
GSE63058 |
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages
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139 | Giuseppe Testa | Dec 15, 2014 | |||
GSE63028 |
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages (aCGH)
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34 | Giuseppe Testa | Dec 15, 2014 | |||
GSE118648 |
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
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31 | Cristina Mecucci | Sep 01, 2019 | |||
GSE65777 |
A Genome Wide Association Study Reveals Genetic Predisposition for Bortezomib-Induced Peripheral Neuropathy in Multiple Myeloma by Variation in the PREP1-CBS locus.
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469 | Wilfried Gouraud | Nov 23, 2016 | |||
GSE85594 |
A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population
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47 | Lynn Jorde | Aug 16, 2016 | |||
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 | |||
GSE54504 |
A Genomic Portrait of Resectable Hepatocellular Carcinomas: Implications of RB1 and FGF19 Aberrations for Patient Stratification.
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462 | Farhan Haq | May 01, 2014 | |||
GSE34573 |
A Global View of the Oncogenic Landscape in Nasopharyngeal Carcinoma:An Integrated Analysis at the Genetic and Expression Levels
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64 | Wenbin Wei | Dec 10, 2012 | |||
GSE59150 |
A High-Resolution Copy Number Variation Resource for Clinical Genetics
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873 | Stephen W Scherer | Jul 24, 2014 | |||
GSE30481 |
A Map of Copy Number Variations in Chinese Populations
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155 | Haiyi Lou | Dec 31, 2011 | |||
GSE133063 |
A Novel Silent Mutation in the L1CAM Gene causing Fetal Hydrocephalus
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1 | yixi sun | Jul 16, 2019 | |||
GSE16122 |
A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma
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203 | Luca Agnelli | May 16, 2009 | |||
GSE14845 |
A Whole Genome Approach to Characterising a Novel Immunodeficiency Disorder
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4 | Michael Richard Green | Apr 01, 2009 | |||
GSE99221 |
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth and senescence escape via regulation of MITF
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126 | Jiyeon Choi | Jul 01, 2017 | |||
GSE7822 |
A comparison of DNA copy number profiling platforms using a panel of melanoma cell lines
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151 | Joel Greshock | Nov 02, 2007 |