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PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations.
Bendl, Jaroslav; Stourac, Jan; Salanda, Ondrej; Pavelka, Antonin; Wieben, Eric D; Zendulka, Jaroslav; Brezovsky, Jan; Damborsky, Jiri.
Afiliación
  • Bendl J; Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic ; Department of Information Systems, Faculty of Information Technology, Brno University of Technology, Brno, Czech Repub
  • Stourac J; Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic ; Center of Biomolecular and Cellular Engineering, International Centre for Clinical Research, St. Anne's University Hos
  • Salanda O; Department of Information Systems, Faculty of Information Technology, Brno University of Technology, Brno, Czech Republic.
  • Pavelka A; Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic.
  • Wieben ED; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, New York, United States of America.
  • Zendulka J; Department of Information Systems, Faculty of Information Technology, Brno University of Technology, Brno, Czech Republic.
  • Brezovsky J; Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic.
  • Damborsky J; Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic ; Center of Biomolecular and Cellular Engineering, International Centre for Clinical Research, St. Anne's University Hos
PLoS Comput Biol ; 10(1): e1003440, 2014 Jan.
Article en En | MEDLINE | ID: mdl-24453961
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biología Computacional / Polimorfismo de Nucleótido Simple / Enfermedades Genéticas Congénitas / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2014 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biología Computacional / Polimorfismo de Nucleótido Simple / Enfermedades Genéticas Congénitas / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2014 Tipo del documento: Article