Interpretation of genetic variants

Research output: Contribution to journalArticlepeer-review

Abstract

Sequencing of the human genome and introduction of clinical next-generation sequencing enable discovery of all DNA variants carried by an individual. Variants may be solely responsible for disease, may contribute to disease, or may have no influence on the development of disease. Interpreting the effect of these variants upon disease is a major challenge for medicine. Although the process is still evolving, certain methods are useful in discriminating the effect of variants upon phenotype. These methods have been employed to the greatest extent in Mendelian disorders where deleterious changes in one gene can cause disease. Here, we briefly review the relative merits of these methods, with emphasis on using a comprehensive approach modelled after the analysis of variants that causes cystic fibrosis.

Original languageEnglish (US)
Pages (from-to)295-297
Number of pages3
JournalThorax
Volume69
Issue number3
DOIs
StatePublished - Mar 2014

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

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