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Items: 3

1.

Hereditary Hearing Loss SNP-Microarray Pilot Study

(Submitter supplied) Objectives: Despite recent advancements in diagnostic tools, the genomic landscape of hereditary hearing loss remains largely uncharacterized. One strategy to understand genome-wide aberrations includes the analysis of copy number variation that can be mapped using SNP-microarray technology. A growing collection of literature has begun to uncover the importance of copy number variation in hereditary hearing loss. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL24663
108 Samples
Download data: CSV, IDAT, TXT, XLS
Series
Accession:
GSE111131
ID:
200111131

PubMed Full text in PMC Similar studies

2.

Illumina HumanOmni1-Quad BeadChip

(Submitter supplied) see manufacturer's website
Organism:
Homo sapiens
1 Series
108 Samples
Download data
Platform
Accession:
GPL24663
ID:
100024663

3.

arr-12-074 Blood

Organism:
Homo sapiens
Source name:
Blood
Platform:
GPL24663
Series:
GSE111131
Download data: IDAT
Sample
Accession:
GSM3022652
ID:
303022652

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db=gds|term=GSM3022652[Accession]|query=1|qty=2|blobid=MCID_6748ef82462e1a751e1515bf|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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