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kinmut2.bioinfo.cnio.es

KinMut2

Submit variants for analysis. WKinMut-2 is an integrated framework for the analysis and interpretation of the consequences of variants in the human kinome. It displays information from diverse sources, that include:. Protein/Gene general information, Gene Ontology terms, estimations of gene essentiality in orthologues and known drug targets. Structural information from PDB and Structure-PPI. Predictions of variant pathogenicity with 9 different methods, including our own kinase-specific Random Forest.

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Submit variants for analysis. WKinMut-2 is an integrated framework for the analysis and interpretation of the consequences of variants in the human kinome. It displays information from diverse sources, that include:. Protein/Gene general information, Gene Ontology terms, estimations of gene essentiality in orthologues and known drug targets. Structural information from PDB and Structure-PPI. Predictions of variant pathogenicity with 9 different methods, including our own kinase-specific Random Forest.
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KinMut2 | kinmut2.bioinfo.cnio.es Reviews

https://kinmut2.bioinfo.cnio.es

Submit variants for analysis. WKinMut-2 is an integrated framework for the analysis and interpretation of the consequences of variants in the human kinome. It displays information from diverse sources, that include:. Protein/Gene general information, Gene Ontology terms, estimations of gene essentiality in orthologues and known drug targets. Structural information from PDB and Structure-PPI. Predictions of variant pathogenicity with 9 different methods, including our own kinase-specific Random Forest.

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Submit variants for analysis. WKinMut-2 is an integrated framework for the analysis and interpretation of the consequences of variants in the human kinome. It displays information from diverse sources, that include:. Protein/Gene general information, Gene Ontology terms, estimations of gene essentiality in orthologues and known drug targets. Structural information from PDB and Structure-PPI. Predictions of variant pathogenicity with 9 different methods, including our own kinase-specific Random Forest.

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