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Items: 3

1.

Acquired mutations in TET2 are common in myelodysplastic syndromes

(Submitter supplied) Myelodysplastic syndromes (MDS) represent a heterogeneous group of neoplastic hematopoietic disorders. Several recurrent chromosomal aberrations have been associated with MDS, but the genes affected have remained largely unknown. To identify relevant genetic lesions involved in the pathogenesis of MDS, we performed SNP-array-based genomic profiling and genomic sequencing in 102 patients. We identified acquired deletions, missense and nonsense mutations in a new gene, TET2, in 26% of MDS patients. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platforms:
GPL3718 GPL6801
122 Samples
Download data: CEL, CHP
Series
Accession:
GSE15688
ID:
200015688
2.

[Mapping250K_Nsp] Affymetrix Mapping 250K Nsp 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...
Organism:
Homo sapiens
193 Series
11192 Samples
Download data
Platform
Accession:
GPL3718
ID:
100003718
3.

UPN02_T-cell

Organism:
Homo sapiens
Source name:
T-cell fraction
Platform:
GPL3718
Series:
GSE15688
Download data: CEL, CHP
Sample
Accession:
GSM392663
ID:
300392663
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db=gds|term=GSM392663[Accession]|query=1|qty=2|blobid=MCID_6748d5e9462e1a751e11cb9f|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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