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Single nucleotide variations: Biological impact and theoretical interpretation
Genome-wide association studies (GWAS) and whole-exome sequencing (WES) generate massive amounts of genomic variant information, and a major challenge is to identify which variations drive disease or contribute to phenotypic traits. Because the majority of known disease-causing mutations are exonic...
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| Publicado no: | Protein Sci |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BlackWell Publishing Ltd
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4253807/ https://ncbi.nlm.nih.gov/pubmed/25234433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pro.2552 |
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