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Items: 3

1.

SNP data from lymphoma samples

(Submitter supplied) B cell non-Hodgkin's lymphoma (B-NHL) consists of different pathological entities that are frequently characterized by distinct genetic alterations. However, the knowledge on these genetic lesions in B-NHL is still limited. In order to obtain a more comprehensive view of genetic lesions in B-NHL, we performed genome-wide analysis of copy number (CN) alterations as well as allelic imbalances using Affymetrix SNP arrays with B-NHL cases, including SNP array data were analyzed with CNAG/AsCNAR software, which enabled sensitive detection of CN alterations in allele-specific manner, and thus allelic imbalances, without depending on availability of paired normal controls. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
4 related Platforms
332 Samples
Download data: CEL, CHP
Series
Accession:
GSE12906
ID:
200012906
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.

MALT003_Mapping250K_Nsp

Organism:
Homo sapiens
Source name:
lymphoma primary specimen
Platform:
GPL3718
Series:
GSE12906
Download data: CEL, CHP
Sample
Accession:
GSM323924
ID:
300323924
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db=gds|term=GSM323924[Accession]|query=5|qty=2|blobid=MCID_66a8228df6f895792d5122f7|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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