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Comprehensive genetic testing with ethnic‐specific filtering by allele frequency in a Japanese hearing‐loss population
Author(s) -
Moteki H.,
Azaiez H.,
Booth K.T.,
Shearer A.E.,
Sloan C. M.,
Kolbe D.L.,
Nishio S.,
Hattori M.,
Usami S.,
Smith R.J.H.
Publication year - 2016
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12677
Subject(s) - proband , genetics , sanger sequencing , allele frequency , minor allele frequency , allele , hearing loss , biology , genetic testing , ethnic group , mutation , gene , medicine , audiology , sociology , anthropology
Recent advances in targeted genomic enrichment with massively parallel sequencing ( TGE + MPS ) have made comprehensive genetic testing for non‐syndromic hearing loss ( NSHL ) possible. After excluding NSHL subjects with causative mutations in GJB2 and the MT‐RNR1 ( 1555A >G) variant by Sanger sequencing, we completed TGE + MPS on 194 probands with presumed NSHL identified across Japan. We used both publicly available minor allele frequency ( MAF ) datasets and ethnic‐specific MAF filtering against an in‐house database of 200 normal‐hearing Japanese controls. Ethnic‐specific MAF filtering allowed us to re‐categorize as common 203 variants otherwise annotated as rare or novel in non‐Japanese ethnicities. This step minimizes false‐positive results and improves the annotation of identified variants. Causative variants were identified in 27% of probands with solve rates of 35%, 35% and 19% for dominant, recessive and sporadic NSHL , respectively. Mutations in MYO15A and CDH23 follow GJB2 as the frequent causes of recessive NSHL ; copy number variations in STRC are a major cause of mild‐to‐moderate NSHL . Ethnic‐specific filtering by allele frequency is essential to optimize the interpretation of genetic data.