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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

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