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VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data
PURPOSE: To develop and validate VisCap, a software program targeted to clinical laboratories for inference and visualization of germ-line copy-number variants (CNVs) from targeted next-generation sequencing data. Genet Med 18 7, 712–719. METHODS: VisCap calculates the fraction of overall sequence c...
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Publicado no: | Genet Med |
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Main Authors: | , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Nature Publishing Group
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4940431/ https://ncbi.nlm.nih.gov/pubmed/26681316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2015.156 |
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