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Items: 3

1.

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

(Submitter supplied) Illumina Infinium whole genome genotyping (WGG) arrays are increasingly being applied in cancer genomics to study gene copy number alterations and allele-specific aberrations such as loss-of-heterozygosity (LOH). Methods developed for normalization of WGG arrays have mostly focused on diploid, normal samples. However, for cancer samples genomic aberrations may confound normalization and data interpretation. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL6981
6 Samples
Download data: TXT
Series
Accession:
GSE11977
ID:
200011977

PubMed Full text in PMC Similar studies

2.

Illumina HumanHap550v3 Genotyping BeadChip (HumanHap550v3_B)

(Submitter supplied) over 555,000 tag SNP markers derived from the International HapMap Project Protocol: See manufacturer's website
Organism:
Homo sapiens
1 Series
2 Related Platforms
6 Samples
Download data: CSV
Platform
Accession:
GPL6981
ID:
100006981

3.

BT4

Organism:
Homo sapiens
Source name:
Breast carcinoma
Platform:
GPL6981
Series:
GSE11977
Download data
Sample
Accession:
GSM302902
ID:
300302902

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db=gds|term=GSM302902[Accession]|query=1|qty=2|blobid=MCID_678be5cbf5211606908d7294|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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