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Computational approaches to interpreting genomic sequence variation
Identifying sequence variants that play a mechanistic role in human disease and other phenotypes is a fundamental goal in human genetics and will be important in translating the results of variation studies. Experimental validation to confirm that a variant causes the biochemical changes responsible...
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| Publicado no: | Genome Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4254438/ https://ncbi.nlm.nih.gov/pubmed/25473426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-014-0087-1 |
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