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BALL-SNP: combining genetic and structural information to identify candidate non-synonymous single nucleotide polymorphisms
BACKGROUND: High-throughput genetic testing is increasingly applied in clinics. Next-Generation Sequencing (NGS) data analysis however still remains a great challenge. The interpretation of pathogenicity of single variants or combinations of variants is crucial to provide accurate diagnostic informa...
Autores principales: | Mueller, Sabine C., Backes, Christina, Kalinina, Olga V., Meder, Benjamin, Stöckel, Daniel, Lenhof, Hans-Peter, Meese, Eckart, Keller, Andreas |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506604/ https://www.ncbi.nlm.nih.gov/pubmed/26191084 http://dx.doi.org/10.1186/s13073-015-0190-y |
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