about
Phased whole-genome genetic risk in a family quartet using a major allele reference sequenceI-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.Bioinformatics for personal genome interpretationThe pros and cons of predicting protein contact maps.A three-state prediction of single point mutations on protein stability changes.Quantifying the relationship between sequence and three-dimensional structure conservation in RNA.Comparative modeling: the state of the art and protein drug target structure prediction.Improving the prediction of disease-related variants using protein three-dimensional structureWALTZ-DB: a benchmark database of amyloidogenic hexapeptides.In silico comparative characterization of pharmacogenomic missense variants.SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease.Collective judgment predicts disease-associated single nucleotide variantsComputational and theoretical methods for protein folding.Hierarchical mechanochemical switches in angiostatin.The WWWH of remote homolog detection: the state of the art.The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules.WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation.Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations.WebRASP: a server for computing energy scores to assess the accuracy and stability of RNA 3D structures.Functional annotations improve the predictive score of human disease-related mutations in proteins.Bioinformatics challenges for personalized medicineSARA-Coffee web server, a tool for the computation of RNA sequence and structure multiple alignmentsComputational methods and resources for the interpretation of genomic variants in cancerBioinformatics and variability in drug response: a protein structural perspective.VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics.VpreB serves as an invariant surrogate antigen for selecting immunoglobulin antigen-binding sites.Blind prediction of deleterious amino acid variations with SNPs&GO.Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.PhD-SNPg: a webserver and lightweight tool for scoring single nucleotide variants.A new disease-specific machine learning approach for the prediction of cancer-causing missense variants.VarI-SIG 2014--From SNPs to variants: interpreting different types of genetic variants.ContrastRank: a new method for ranking putative cancer driver genes and classification of tumor samples.SARA: a server for function annotation of RNA structures.All-atom knowledge-based potential for RNA structure prediction and assessment.A neural-network-based method for predicting protein stability changes upon single point mutations.Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.Dynamics of the minimally frustrated helices determine the hierarchical folding of small helical proteins.Using tertiary structure for the computation of highly accurate multiple RNA alignments with the SARA-Coffee package.RNA structure alignment by a unit-vector approach.Predicting protein stability changes from sequences using support vector machines.
P50
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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type
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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prefLabel
Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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Emidio Capriotti
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P1053
D-9318-2011
P106
P1153
8851983500
P21
P2456
P31
P3829
P496
0000-0002-2323-0963