283 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 filterCHP
GSE118648
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
31 Cristina Mecucci Sep 01, 2019
GSE85594
A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population
47 Lynn Jorde Aug 16, 2016
GSE34573
A Global View of the Oncogenic Landscape in Nasopharyngeal Carcinoma:An Integrated Analysis at the Genetic and Expression Levels
64 Wenbin Wei Dec 10, 2012
GSE14845
A Whole Genome Approach to Characterising a Novel Immunodeficiency Disorder
4 Michael Richard Green Apr 01, 2009
GSE21349
A compendium of myeloma associated chromosomal copy number abnormalities and their prognostic value
491 Brian A Walker Oct 18, 2010
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
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
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
GSE75358
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
36 Raif S. Geha Nov 25, 2015
GSE75314
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family A)
32 Raif S. Geha Nov 25, 2015
GSE243056
A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias
19 Cristina Mecucci Apr 30, 2024
GSE20206
Acquired chromosome abnormalities in the lungs of patients with Pulmonary Arterial Hypertension
37 Christopher D Coldren May 01, 2010
GSE15688
Acquired mutations in TET2 are common in myelodysplastic syndromes
  • Genome variation profiling by SNP array
122 Roland P. Kuiper May 28, 2009
GSE30255
Activation of ERBB2 signaling causes resistance to the EGFR-directed therapeutic antibody cetuximab
  • Genome variation profiling by SNP array
5 Pasi Antero Jänne Nov 23, 2011
GSE19996
Affy SNP-array data for 23 ETV6/RUNX1-positive ALL patient samples and one cell line
48 Henrik Lilljebjörn Jul 07, 2010
GSE17534
Affymetrix 250K StyI SNP array data from PBMCs and cell lines of metastatic melanoma patients
104 Andreas Gast Apr 13, 2010
GSE28684
Affymetrix 500K SNP array data for Primary Effusion Lymphoma samples
32 Dirk Dittmer Jun 23, 2011
GSE15826
Affymetrix 6.0 study of sporadic motor neuron disease patients and controls.
164 Roger Pamphlett Jul 31, 2010
GSE50024
Affymetrix SNP 6.0 array data for Diffuse Intrinsic Pontine Glioma
72 Pawel Buczkowicz Mar 31, 2014