Harmonizing the interpretation of genetic variants across the world: the Malaysian experience

BACKGROUND: Databases for gene variants are very useful for sharing genetic data and to facilitate the understanding of the genetic basis of diseases. This report summarises the issues surrounding the development of the Malaysian Human Variome Project Country Node. The focus is on human germline var...

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Detalles Bibliográficos
Autores principales: Nik Hassan, Nik Norliza, Plazzer, John-Paul, Smith, Timothy D., Halim-Fikri, Hashim, Macrae, Finlay, Zubaidi AL, A., Zilfalil, Bin Alwi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768322/
https://www.ncbi.nlm.nih.gov/pubmed/26915360
http://dx.doi.org/10.1186/s13104-015-1798-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768322/
https://www.ncbi.nlm.nih.gov/pubmed/26915360
http://dx.doi.org/10.1186/s13104-015-1798-0

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