none6noIn silico approaches are routinely adopted to predict the effects of genetic variants and their relation to diseases. The critical assessment of genome interpretation (CAGI) has established a common framework for the assessment of available predictors of variant effects on specific problems and our group has been an active participant of CAGI since its first edition. In this paper, we summarize our experience and lessons learned from the last edition of the experiment (CAGI-5). In particular, we analyze prediction performances of our tools on five CAGI-5 selected challenges grouped into three different categories: prediction of variant effects on protein stability, prediction of variant pathogenicity, and prediction of complex functi...
The NAGLU challenge of the fourth edition of the Critical Assessment of Genome Interpretation experi...
The sequencing of the human genome has opened up completely new avenues in research and the notion o...
Accurate prediction of the impact of genomic variation on phenotype is a major goal of computational...
In silico approaches are routinely adopted to predict the effects of genetic variants and their rela...
Computational tools are widely used for ranking and prioritizing variants for characterizing their d...
Correct phenotypic interpretation of variants of unknown significance for cancer-associated genes is...
The CAGI-5 pericentriolar material 1 (PCM1) challenge aimed to predict the effect of 38 transgenic h...
The CAGI-5 pericentriolar material 1 (PCM1) challenge aimed to predict the effect of 38 transgenic h...
Whole-genome sequencing (WGS) holds great potential as a diagnostic test. However, the majority of p...
The availability of disease-specific genomic data is critical for developing new computational metho...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine and sequence-based clinical diagnostics seek to predict disease risk or to identi...
The NAGLU challenge of the fourth edition of the Critical Assessment of Genome Interpretation experi...
The sequencing of the human genome has opened up completely new avenues in research and the notion o...
Accurate prediction of the impact of genomic variation on phenotype is a major goal of computational...
In silico approaches are routinely adopted to predict the effects of genetic variants and their rela...
Computational tools are widely used for ranking and prioritizing variants for characterizing their d...
Correct phenotypic interpretation of variants of unknown significance for cancer-associated genes is...
The CAGI-5 pericentriolar material 1 (PCM1) challenge aimed to predict the effect of 38 transgenic h...
The CAGI-5 pericentriolar material 1 (PCM1) challenge aimed to predict the effect of 38 transgenic h...
Whole-genome sequencing (WGS) holds great potential as a diagnostic test. However, the majority of p...
The availability of disease-specific genomic data is critical for developing new computational metho...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using th...
Precision medicine and sequence-based clinical diagnostics seek to predict disease risk or to identi...
The NAGLU challenge of the fourth edition of the Critical Assessment of Genome Interpretation experi...
The sequencing of the human genome has opened up completely new avenues in research and the notion o...
Accurate prediction of the impact of genomic variation on phenotype is a major goal of computational...