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Items: 3

1.

A Genome-wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Possibilities for Future Personalized Treatment

(Submitter supplied) In colorectal cancer (CRC), chromosomal instability (CIN) is typically studied using comparative-genomic hybridization (CGH) arrays. We studied paired (tumor and surrounding healthy) fresh-frozen tissue from 86 CRC patients using Illumina’s Infinium-based SNP array. This method allowed us to study CIN in CRC, with simultaneous analysis of copy number (CN) and B-allele frequency (BAF), which is a representation of allelic composition. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL8887 GPL13829
172 Samples
Download data: TXT
Series
Accession:
GSE34678
ID:
200034678
2.

Illumina HumanCytoSNP-12 v2.1 BeadChip

(Submitter supplied) See manufacturer's website
Organism:
Homo sapiens
56 Series
3148 Samples
Download data
Platform
Accession:
GPL13829
ID:
100013829
3.

Colon Tissue Sample_62

Organism:
Homo sapiens
Source name:
Colon tissue, tumor
Platform:
GPL13829
Series:
GSE34678
Download data
Sample
Accession:
GSM853326
ID:
300853326
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Supplemental Content

db=gds|term=GSM853326[Accession]|query=1|qty=2|blobid=MCID_66a1586656cb0a044ea8f659|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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