GSM472851[Accession] - GEO DataSets

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Items: 3

Select item 2000191011.

Identification of Acquired Copy Number Alterations and Uniparental Disomies in Cytogenetically Normal AML

(Submitter supplied) Identification of Acquired Copy Number Alterations and Uniparental Disomies in Cytogenetically Normal Acute Myeloid Leukemia Using High-Resolution Single Nucleotide Polymorphism Analysis Recent advances in genome-wide single nucleotide polymorphism (SNP) analyses have revealed previously unrecognized microdeletions and uniparental disomy (UPD) in a broad spectrum of human cancers. As acute myeloid leukemia (AML) represents a genetically heterogeneous disease, this technology might prove helpful especially for cytogenetically normal AML (CN-AML) cases. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by SNP array

4 related Platforms
510 Samples

Download data: CEL, CHP, TXT

Series

Accession:: GSE19101

ID:: 200019101

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Select item 1000037202.

[Mapping250K_Sty] Affymetrix Mapping 250K Sty2 SNP Array

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://www.ncbi.nlm.nih.gov/projects/geo/info/geo_affy.html The GeneChip® Human Mapping 500K Array Set provides consistently high coverage across different populations. It is comprised of two arrays, each capable of genotyping on average 250,000 SNPs (approximately 262,000 for Nsp arrays and 238,000 for Sty arrays). more...