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Items: 3

1.

Analysis of copy number changes and complex rearrangements in patients with congenital abnormalities

(Submitter supplied) Chromothripsis represents a novel phenomenon in the structural variation landscape of cancer genomes. Here, we analyzed the genomes of ten patients with congenital disease that were preselected to carry complex chromosomal rearrangements (CCRs) with more than two breakpoints. The rearrangements displayed unanticipated complexity resembling chromothripsis. We find that eight of them contain hallmarks of multiple clustered double-stranded DNA breaks (DSBs) on one or more chromosomes. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL8855 GPL6979 GPL6985
13 Samples
Download data: TXT
Series
Accession:
GSE37906
ID:
200037906

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2.

Illumina HumanHap300v1 Genotyping BeadChip (HumanHap300_(v1.0.0))

(Submitter supplied) over 317,000 tagSNP markers derived from the International HapMap Project Protocol: See manufacturer's website
Organism:
Homo sapiens
2 Series
80 Samples
Download data: CSV
Platform
Accession:
GPL6979
ID:
100006979

3.

Patient5_mother

Organism:
Homo sapiens
Source name:
DNA from blood, patient 5 mother
Platform:
GPL6979
Series:
GSE37906
Download data
Sample
Accession:
GSM929765
ID:
300929765

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db=gds|term=GSM929765[Accession]|query=1|qty=2|blobid=MCID_673391e15c1af07374741212|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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