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Analysis of pathogenic variants from the ClinVar database in healthy people using next-generation sequencing
Next-generation sequencing (NGS) became an effective approach for finding novel causative genomic variants of genetic disorders and is increasingly used for diagnostic purposes. Public variant databases that gather data of pathogenic variants are being relied upon as a source for clinical diagnosis....
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| Publicado no: | Genet Res (Camb) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cambridge University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6865174/ https://ncbi.nlm.nih.gov/pubmed/28851476 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0016672317000040 |
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