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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Shranjeno v:
Bibliografske podrobnosti
izdano v:BMC Res Notes
Main Authors: Nik Hassan, Nik Norliza, Plazzer, John-Paul, Smith, Timothy D., Halim-Fikri, Hashim, Macrae, Finlay, Zubaidi AL, A., Zilfalil, Bin Alwi
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Short Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4768322/
https://ncbi.nlm.nih.gov/pubmed/26915360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1798-0
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