Interpretation of personal genome sequencing data in terms of disease ranks based on mutual information

BACKGROUND: The rapid advances in genome sequencing technologies have resulted in an unprecedented number of genome variations being discovered in humans. However, there has been very limited coverage of interpretation of the personal genome sequencing data in terms of diseases. METHODS: In this pap...

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Detalles Bibliográficos
Autores principales: Na, Young-Ji, Sohn, Kyung-Ah, Kim, Ju Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460593/
https://www.ncbi.nlm.nih.gov/pubmed/26045178
http://dx.doi.org/10.1186/1755-8794-8-S2-S4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460593/
https://www.ncbi.nlm.nih.gov/pubmed/26045178
http://dx.doi.org/10.1186/1755-8794-8-S2-S4

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