Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

ABSTRACT: In order to provide a faster, more comprehensive and cost effective assay, we constructed a DNA fluidic array, CapitalBioMiamiOtoArray, for the detection of sequence variants in five genes that are common in most populations of European descent. Our results show 100% concordance between the fluidic array biochip-based approach and the established Sanger sequencing method, thus proving its robustness and reliability at a relatively low cost.

ORGANISM(S): Homo sapiens

PROVIDER: GSE94994 | GEO | 2017/02/17

SECONDARY ACCESSION(S): PRJNA375095

REPOSITORIES: GEO