|
|
Single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data
|
|
|
|
|
نویسنده
|
Yu Chenglong ,Baune Bernhard T ,Licinio Julio ,Wong Ma-Li
|
منبع
|
journal of human genetics - 2017 - دوره : 62 - شماره : 5 - صفحه:577 -580
|
چکیده
|
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.
|
|
|
آدرس
|
South Australian Health and Medical Research Institute, Australia. Flinders University, Australia, University of Adelaide, Australia, South Australian Health and Medical Research Institute, Australia. Flinders University, Australia, South Australian Health and Medical Research Institute, Australia. Flinders University, Australia
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Authors
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|