Using whole-exome sequencing to identify variants inherited from mosaic parents

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Whole-exome sequencing (WES) has allowed the discovery of genes and variants causing rare human disease. This is often achieved by comparing nonsynonymous variants between unrelated patients, and particularly for sporadic or recessive disease, often identifies a single or few candidate genes for further consideration. However, despite the potential for this approach to elucidate the genetic cause of rare human disease, a majority of patients fail to realize a genetic diagnosis using standard exome analysis methods. Although genetic heterogeneity contributes to the difficulty of exome sequence analysis between patients, it remains plausible that rare human disease is not caused by de novo or recessive variants. Multiple human disorders have been described for which the variant was inherited from a phenotypically normal mosaic parent. Here we highlight the potential for exome sequencing to identify a reasonable number of candidate genes when dominant disease variants are inherited from a mosaic parent. We show the power of WES to identify a limited number of candidate genes using this disease model and how sequence coverage affects identification of mosaic variants by WES. We propose this analysis as an alternative to discover genetic causes of rare human disorders for which typical WES approaches fail to identify likely pathogenic variants.

Original languageEnglish (US)
Pages (from-to)547-550
Number of pages4
JournalEuropean Journal of Human Genetics
Volume23
Issue number4
DOIs
StatePublished - Apr 14 2015

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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