Hereditary hearing loss SNP-microarray pilot study

Hereditary hearing loss SNP-microarray pilot study

Abstract 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....

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Bibliographic Details
Main Authors: Barbara Vona, Michaela A. H. Hofrichter, Jörg Schröder, Wafaa Shehata-Dieler, Indrajit Nanda, Thomas Haaf
Format: Article
Language:English
Published: BMC 2018-06-01
Series:BMC Research Notes
Subjects:
Copy number variation
Genotyping arrays
Hereditary hearing loss
Infinium HumanOmni1-Quad
Illumina
SNP-microarray
Online Access:http://link.springer.com/article/10.1186/s13104-018-3466-7

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