Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases

Human genome variation may cause differences in traits and disease risks. Disease-causal/susceptible genes and variants for both common and rare diseases can be detected by comprehensive whole-genome analyses, such as whole-genome sequencing (WGS), using next-generation sequencing (NGS) technology a...

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Detalles Bibliográficos
Autores principales: HITOMI, Yuki, TOKUNAGA, Katsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743846/
https://www.ncbi.nlm.nih.gov/pubmed/29129848
http://dx.doi.org/10.2183/pjab.93.042

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743846/
https://www.ncbi.nlm.nih.gov/pubmed/29129848
http://dx.doi.org/10.2183/pjab.93.042

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