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FLAGS, frequently mutated genes in public exomes
BACKGROUND: Dramatic improvements in DNA-sequencing technologies and computational analyses have led to wide use of whole exome sequencing (WES) to identify the genetic basis of Mendelian disorders. More than 180 novel rare-disease-causing genes with Mendelian inheritance patterns have been discover...
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| Publicat a: | BMC Med Genomics |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4267152/ https://ncbi.nlm.nih.gov/pubmed/25466818 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-014-0064-y |
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