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Items: 3

1.

Evaluation of copy number variation detection between high-resolution array CGH and low-coverage short-insert and mate-pair whole-genome sequencing

(Submitter supplied) In principle, whole-genome sequencing (WGS) of the human genome even at low coverage offers higher resolution for genomic copy number variation (CNV) detection compared to array-based technologies, which is currently the first-tier approach in clinical cytogenetics. There are, however, obstacles in replacing array-based CNV detection with that of low-coverage WGS such as cost, turnaround time, and lack of systematic performance comparisons. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL24127
2 Samples
Download data: IDAT
Series
Accession:
GSE105092
ID:
200105092

PubMed Full text in PMC Similar studies Analyze with GEO2R

2.

Illumina Infinium Multi-Ethnic Global-8 v1.0 Array

(Submitter supplied) See manufacturer's website
Organism:
Homo sapiens
5 Series
113 Samples
Download data: CSV
Platform
Accession:
GPL24127
ID:
100024127

3.

NA16595_rep1

Organism:
Homo sapiens
Source name:
DNA from Coriell
Platform:
GPL24127
Series:
GSE105092
Download data: IDAT
Sample
Accession:
GSM2817863
ID:
302817863

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db=gds|term=GSM2817863[Accession]|query=1|qty=2|blobid=MCID_66df22adfadf6d74e1212e52|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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