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VCF.Filter: interactive prioritization of disease-linked genetic variants from sequencing data
Next generation sequencing is widely used to link genetic variants to diseases, and it has massively accelerated the diagnosis and characterization of rare genetic diseases. After initial bioinformatic data processing, the interactive analysis of genome, exome, and panel sequencing data typically st...
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| Publicado no: | Nucleic Acids Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5570181/ https://ncbi.nlm.nih.gov/pubmed/28520890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx425 |
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