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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
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| 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 |