Pages that link to "Q42034988"
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The following pages link to Emidio Capriotti (Q42034988):
Displaying 50 items.
- Phased whole-genome genetic risk in a family quartet using a major allele reference sequence (Q21144940) (← links)
- I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure (Q24812223) (← links)
- Bioinformatics for personal genome interpretation (Q28728835) (← links)
- The pros and cons of predicting protein contact maps. (Q30366465) (← links)
- A three-state prediction of single point mutations on protein stability changes. (Q30368637) (← links)
- Quantifying the relationship between sequence and three-dimensional structure conservation in RNA. (Q30390338) (← links)
- Comparative modeling: the state of the art and protein drug target structure prediction (Q30402152) (← links)
- Improving the prediction of disease-related variants using protein three-dimensional structure (Q30408049) (← links)
- WALTZ-DB: a benchmark database of amyloidogenic hexapeptides (Q30487585) (← links)
- In silico comparative characterization of pharmacogenomic missense variants (Q30583473) (← links)
- SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease (Q34324911) (← links)
- Collective judgment predicts disease-associated single nucleotide variants (Q34354991) (← links)
- Computational and theoretical methods for protein folding (Q34382310) (← links)
- Hierarchical mechanochemical switches in angiostatin (Q34567943) (← links)
- The WWWH of remote homolog detection: the state of the art. (Q34569115) (← links)
- The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules (Q34664947) (← links)
- WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation (Q34789974) (← links)
- Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations (Q34790453) (← links)
- WebRASP: a server for computing energy scores to assess the accuracy and stability of RNA 3D structures (Q34912135) (← links)
- Functional annotations improve the predictive score of human disease-related mutations in proteins (Q34985914) (← links)
- Bioinformatics challenges for personalized medicine (Q35051893) (← links)
- SARA-Coffee web server, a tool for the computation of RNA sequence and structure multiple alignments (Q35196689) (← links)
- Computational methods and resources for the interpretation of genomic variants in cancer (Q35674603) (← links)
- Bioinformatics and variability in drug response: a protein structural perspective (Q36009999) (← links)
- VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics (Q36064333) (← links)
- VpreB serves as an invariant surrogate antigen for selecting immunoglobulin antigen-binding sites (Q37649940) (← links)
- Blind prediction of deleterious amino acid variations with SNPs&GO. (Q38437989) (← links)
- Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI. (Q38691170) (← links)
- PhD-SNPg: a webserver and lightweight tool for scoring single nucleotide variants (Q38798043) (← links)
- A new disease-specific machine learning approach for the prediction of cancer-causing missense variants (Q42034929) (← links)
- VarI-SIG 2014--From SNPs to variants: interpreting different types of genetic variants (Q42407061) (← links)
- ContrastRank: a new method for ranking putative cancer driver genes and classification of tumor samples (Q42565283) (← links)
- SARA: a server for function annotation of RNA structures (Q43103662) (← links)
- All-atom knowledge-based potential for RNA structure prediction and assessment (Q45783105) (← links)
- A neural-network-based method for predicting protein stability changes upon single point mutations. (Q45966727) (← links)
- Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans (Q46952242) (← links)
- Dynamics of the minimally frustrated helices determine the hierarchical folding of small helical proteins (Q47221982) (← links)
- Using tertiary structure for the computation of highly accurate multiple RNA alignments with the SARA-Coffee package (Q47910888) (← links)
- RNA structure alignment by a unit-vector approach (Q48327178) (← links)
- Predicting protein stability changes from sequences using support vector machines (Q48472134) (← links)
- K-Fold: a tool for the prediction of the protein folding kinetic order and rate (Q51927801) (← links)
- A minimal model of three-state folding dynamics of helical proteins (Q51937338) (← links)
- A Shannon entropy-based filter detects high- quality profile-profile alignments in searches for remote homologues. (Q52005742) (← links)
- Diffusion-collision of foldons elucidates the kinetic effects of point mutations and suggests control strategies of the folding process of helical proteins (Q56997925) (← links)
- Integrating molecular networks with genetic variant interpretation for precision medicine (Q90478903) (← links)
- Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI-5 (Q91509994) (← links)
- DDGun: an untrained method for the prediction of protein stability changes upon single and multiple point variations (Q91560858) (← links)
- Assessing predictions on fitness effects of missense variants in calmodulin (Q91702639) (← links)
- Are machine learning based methods suited to address complex biological problems? Lessons from CAGI-5 challenges (Q91842736) (← links)
- Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variants (Q91845107) (← links)