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Functional modules, mutational load and human genetic disease
The ability to generate a massive amount of sequencing and genotyping data is transforming the study of human genetic disorders. Driven by such innovation, it is likely that whole exome and whole-genome resequencing will replace regionally focused approaches for gene discovery and clinical testing i...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3740181/ https://ncbi.nlm.nih.gov/pubmed/20226561 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2010.01.006 |
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