Cargando…
CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations
Exome sequencing is now mainstream in clinical practice. However, identification of pathogenic Mendelian variants remains time-consuming, in part, because the limited accuracy of current computational prediction methods requires manual classification by experts. Here we introduce CAPICE, a new machi...
Autores principales: | Li, Shuang, van der Velde, K. Joeri, de Ridder, Dick, van Dijk, Aalt D. J., Soudis, Dimitrios, Zwerwer, Leslie R., Deelen, Patrick, Hendriksen, Dennis, Charbon, Bart, van Gijn, Marielle E., Abbott, Kristin, Sikkema-Raddatz, Birgit, van Diemen, Cleo C., Kerstjens-Frederikse, Wilhelmina S., Sinke, Richard J., Swertz, Morris A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446154/ https://www.ncbi.nlm.nih.gov/pubmed/32831124 http://dx.doi.org/10.1186/s13073-020-00775-w |
Ejemplares similares
-
Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital
por: Imafidon, Miriam E., et al.
Publicado: (2021) -
A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature
por: van der Velde, K. Joeri, et al.
Publicado: (2020) -
GAVIN: Gene-Aware Variant INterpretation for medical sequencing
por: van der Velde, K. Joeri, et al.
Publicado: (2017) -
Feasibility of predicting allele specific expression from DNA sequencing using machine learning
por: Zhang, Zhenhua, et al.
Publicado: (2021) -
Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis
por: Deelen, Patrick, et al.
Publicado: (2019)