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BrowseVCF: a web-based application and workflow to quickly prioritize disease-causative variants in VCF files
Following variant calling and annotation, accurate variant filtering is a crucial step to extract meaningful information from sequencing data and to investigate disease aetiology. However, the variant call format (VCF) used to store this information is not easy to handle for non-bioinformaticians. W...
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| Publicado no: | Brief Bioinform |
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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/PMC5862253/ https://ncbi.nlm.nih.gov/pubmed/27373737 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbw054 |
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