Single-nucleotide variant proportion in genes: A new concept to explore major depression based on DNA sequencing data

Chenglong Yu, Bernhard T. Baune, Julio Licinio, Ma Li Wong

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Major depressive disorder (MDD) is a common psychiatric illness with significant medical and socioeconomic impact. Genetic factors are likely to play important roles in the development of this condition. DNA sequencing technology has the ability to identify all private genetic mutations and provides new channels for studying the biology of MDD. In this proof-of-concept study we proposed a novel concept, single-nucleotide variant proportion (SNVP), to investigate MDD based on whole-genome sequencing (WGS) data. Our SNVP-based approach can be used to test newly found candidate genes as a complement to genome-wide genotyping analysis. Furthermore, we performed cluster analysis for MDD patients and ethnically matched healthy controls, and found that clusters based on SNVP may predict MDD diagnosis. Our results suggest that SNVP may be used as a potential biomarker associated with major depression. Our methodology could be a valuable predictive/diagnostic tool as one can test whether a new subject falls within or close to an existing MDD cluster. Advances in this study design have the potential to personalized treatments and could include the ability to diagnose patients based on their full or part DNA sequencing data.

LanguageEnglish
Pages577-580
Number of pages4
JournalJournal of Human Genetics
Volume62
Issue number5
DOIs
Publication statusPublished - 1 Apr 2017

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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