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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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| Publicado no: | BMC Med Genomics |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4460593/ https://ncbi.nlm.nih.gov/pubmed/26045178 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8794-8-S2-S4 |
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