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Items: 3

1.

Comparative genomic hybridization of BRCAX breast tumors

(Submitter supplied) Only about 25% of familial breast cancer is explained by mutations in BRCA1 and BRCA2, fewer by moderate penetrance genes like P53, PTEN, CHEK2, ATM and PALB2 and an unknown fraction by common variants of genes with low penetrance. Evidence suggests that additional dominant breast cancer genes exist and these are referred to as BRCAX. Clinical presentation of families with highly increased incidence of breast cancer that are non-BRCA1/BRCA2, suggests dominant inheritance of such high penetrance breast cancer genes. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL4560
106 Samples
Download data: TXT
Series
Accession:
GSE18626
ID:
200018626
2.

Netherlands Cancer Institute human 3.5k BAC array

(Submitter supplied) Slides: Code Link Activated Slides (Amersham Biosciences, Prod. No. 300011 00) Protocol: Degenerate oligonucleotide PCR-products from all BAC clones were prepared for spotting according to detailed protocols (Pinkel et al, 1998) with some modifications (Alers et al, 1999). All clones (three replicates for each probe) were spotted in randomised fashion across 48 subarrays, each containing 270 spots.
Organism:
Homo sapiens
11 Series
582 Samples
Download data
Platform
Accession:
GPL4560
ID:
100004560
3.

non-BRCA1/2 hereditary breast tumor (BRCAx)_BX403_HB376-13

Organism:
Homo sapiens
Source name:
FFPE primary breast tumor material BRCAx family (channel 1) genomic DNA from blood from 8 healthy females (channel 2)
Platform:
GPL4560
Series:
GSE18626
Download data: TXT
Sample
Accession:
GSM462909
ID:
300462909
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db=gds|term=GSM462909[Accession]|query=4|qty=2|blobid=MCID_672a74ff098d4d34592502bc|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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