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Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations
Accurate methods to assess the pathogenicity of mutations are needed to fully leverage the possibilities of genome sequencing in diagnosis. Current data-driven and bioinformatics approaches are, however, limited by the large number of new variations found in each newly sequenced genome, and often do...
Autores principales: | Nielsen, Sofie V., Stein, Amelie, Dinitzen, Alexander B., Papaleo, Elena, Tatham, Michael H., Poulsen, Esben G., Kassem, Maher M., Rasmussen, Lene J., Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415204/ https://www.ncbi.nlm.nih.gov/pubmed/28422960 http://dx.doi.org/10.1371/journal.pgen.1006739 |
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