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Computational and statistical approaches to analyzing variants identified by exome sequencing
New sequencing technology has enabled the identification of thousands of single nucleotide polymorphisms in the exome, and many computational and statistical approaches to identify disease-association signals have emerged.
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3308043/ https://ncbi.nlm.nih.gov/pubmed/21920052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2011-12-9-227 |
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