Found: 59
Select item for more details and to access through your institution.
Identification of Driver Epistatic Gene Pairs Combining Germline and Somatic Mutations in Cancer.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 11, p. 9323, doi. 10.3390/ijms24119323
- By:
- Publication type:
- Article
Analysis and Interpretation of the Impact of Missense Variants in Cancer.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 11, p. 5416, doi. 10.3390/ijms22115416
- By:
- Publication type:
- Article
The complex impact of cancer-related missense mutations on the stability and on the biophysical and biochemical properties of MAPK1 and MAPK3 somatic variants.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00544-x
- By:
- Publication type:
- Article
Evaluating the relevance of sequence conservation in the prediction of pathogenic missense variants.
- Published in:
- Human Genetics, 2022, v. 141, n. 10, p. 1649, doi. 10.1007/s00439-021-02419-4
- By:
- Publication type:
- Article
PhD-SNP<sup>g</sup>: a webserver and lightweight tool for scoring single nucleotide variants.
- Published in:
- Nucleic Acids Research, 2017, v. 45, n. W1, p. W247, doi. 10.1093/nar/gkx369
- By:
- Publication type:
- Article
SARA-Coffee web server, a tool for the computation of RNA sequence and structure multiple alignments.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. W1, p. W356, doi. 10.1093/nar/gku459
- By:
- Publication type:
- Article
SARA: a server for function annotation of RNA structures.
- Published in:
- Nucleic Acids Research, 2009, v. 37, n. suppl_2, p. W260, doi. 10.1093/nar/gkp433
- By:
- Publication type:
- Article
The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules.
- Published in:
- Nature Structural & Molecular Biology, 2011, v. 18, n. 1, p. 107, doi. 10.1038/nsmb.1936
- By:
- Publication type:
- Article
Calibrating variant-scoring methods for clinical decision making.
- Published in:
- Bioinformatics, 2020, v. 36, n. 24, p. 5709, doi. 10.1093/bioinformatics/btaa943
- By:
- Publication type:
- Article
Bioinformatics for personal genome interpretation.
- Published in:
- Briefings in Bioinformatics, 2012, v. 13, n. 4, p. 495, doi. 10.1093/bib/bbr070
- By:
- Publication type:
- Article
The WWWH of remote homolog detection: The state of the art.
- Published in:
- Briefings in Bioinformatics, 2007, v. 8, n. 2, p. 78, doi. 10.1093/bib/bb1032
- By:
- Publication type:
- Article
Diffusion-collision of foldons elucidates the kinetic effects of point mutations and suggests control strategies of the folding process of helical proteins.
- Published in:
- Proteins, 2006, v. 64, n. 1, p. 198, doi. 10.1002/prot.20980
- By:
- Publication type:
- Article
A Shannon entropy-based filter detects high- quality profileprofile alignments in searches for remote homologues.
- Published in:
- Proteins, 2004, v. 54, n. 2, p. 351
- By:
- Publication type:
- Article
VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics.
- Published in:
- 2016
- By:
- Publication type:
- Proceeding
Improving the prediction of disease-related variants using protein three-dimensional structure.
- Published in:
- BMC Bioinformatics, 2011, v. 12, p. 1, doi. 10.1186/1471-2105-12-S4-S3
- By:
- Publication type:
- Article
Quantifying the relationship between sequenceand three-dimensional structure conservation inRNA.
- Published in:
- BMC Bioinformatics, 2010, v. 11, p. 322, doi. 10.1186/1471-2105-11-322
- By:
- Publication type:
- Article
A three-state prediction of single point mutations on protein stability changes.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-S2-S6
- By:
- Publication type:
- Article
I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.
- Published in:
- Nucleic Acids Research, 2005, v. 33, n. suppl 2, p. w306, doi. 10.1093/nar/gki375
- By:
- Publication type:
- Article
DDGun: an untrained method for the prediction of protein stability changes upon single and multiple point variations.
- Published in:
- BMC Bioinformatics, 2019, v. 20, p. N.PAG, doi. 10.1186/s12859-019-2923-1
- By:
- Publication type:
- Article
VpreB serves as an invariant surrogate antigen for selecting immunoglobulin antigen-binding sites.
- Published in:
- Science Immunology, 2016, v. 1, n. 1, p. 1, doi. 10.1126/sciimmunol.aaf6628
- By:
- Publication type:
- Article
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset.
- Published in:
- Briefings in Bioinformatics, 2022, v. 23, n. 2, p. 1, doi. 10.1093/bib/bbab555
- By:
- Publication type:
- Article
Predicting protein stability changes from sequences using support vector machines.
- Published in:
- Bioinformatics, 2005, v. 21, p. ii54, doi. 10.1093/bioinformatics/bti1109
- By:
- Publication type:
- Article
A neural-network-based method for predicting protein stability changes upon single point mutations.
- Published in:
- Bioinformatics, 2004, v. 20, n. suppl_1, p. i63, doi. 10.1093/bioinformatics/bth928
- By:
- Publication type:
- Article
A neural-network-based method for predicting protein stability changes upon single point mutations.
- Published in:
- Bioinformatics, 2004, v. 20, p. i63, doi. 10.1093/bioinformatics/bth928
- By:
- Publication type:
- Article
PhD-SNPg: updating a webserver and lightweight tool for scoring nucleotide variants.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. W1, p. W451, doi. 10.1093/nar/gkad455
- By:
- Publication type:
- Article
DDGun: an untrained predictor of protein stability changes upon amino acid variants.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. W1, p. W222, doi. 10.1093/nar/gkac325
- By:
- Publication type:
- Article
Fido-SNP: the first webserver for scoring the impact of single nucleotide variants in the dog genome.
- Published in:
- Nucleic Acids Research, 2019, v. 47, n. W1, p. W136, doi. 10.1093/nar/gkz420
- By:
- Publication type:
- Article
VarI-COSI 2018: a forum for research advances in variant interpretation and diagnostics.
- Published in:
- 2019
- By:
- Publication type:
- Editorial
Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002280
- By:
- Publication type:
- Article
Assessing computational predictions of the phenotypic effect of cystathionine‐beta‐synthase variants.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1530, doi. 10.1002/humu.23868
- By:
- Publication type:
- Article
Assessing predictions on fitness effects of missense variants in calmodulin.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1463, doi. 10.1002/humu.23857
- By:
- Publication type:
- Article
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI‐5.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1474, doi. 10.1002/humu.23856
- By:
- Publication type:
- Article
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1612, doi. 10.1002/humu.23849
- By:
- Publication type:
- Article
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1314, doi. 10.1002/humu.23825
- By:
- Publication type:
- Article
Characterization of human frataxin missense variants in cancer tissues.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1400, doi. 10.1002/humu.23789
- By:
- Publication type:
- Article
Are machine learning based methods suited to address complex biological problems? Lessons from CAGI‐5 challenges.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1455, doi. 10.1002/humu.23784
- By:
- Publication type:
- Article
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.
- Published in:
- Human Mutation, 2017, v. 38, n. 9, p. 1042, doi. 10.1002/humu.23235
- By:
- Publication type:
- Article
Blind prediction of deleterious amino acid variations with SNPs&GO.
- Published in:
- Human Mutation, 2017, v. 38, n. 9, p. 1064, doi. 10.1002/humu.23179
- By:
- Publication type:
- Article
Functional annotations improve the predictive score of human disease-related mutations in proteins.
- Published in:
- 2009
- By:
- Publication type:
- Other
Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.
- Published in:
- Human Mutation, 2008, v. 29, n. 1, p. 198, doi. 10.1002/humu.20628
- By:
- Publication type:
- Article
A Deep-Learning Sequence-Based Method to Predict Protein Stability Changes Upon Genetic Variations.
- Published in:
- Genes, 2021, v. 13, n. 6, p. 911, doi. 10.3390/genes12060911
- By:
- Publication type:
- Article
Computational methods and resources for the interpretation of genomic variants in cancer.
- Published in:
- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/1471-2164-16-S8-S7
- By:
- Publication type:
- Article
VarI-SIG 2014 - From SNPs to variants: interpreting different types of genetic variants.
- Published in:
- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/1471-2164-16-S8-I1
- By:
- Publication type:
- Article
SNP-SIG 2013: from coding to non-coding - new approaches for genomic variant interpretation.
- Published in:
- BMC Genomics, 2014, v. 15, p. 1, doi. 10.1186/1471-2164-15-S4-S1
- By:
- Publication type:
- Article
In silico comparative characterization of pharmacogenomic missense variants.
- Published in:
- BMC Genomics, 2014, v. 15, p. 1, doi. 10.1186/1471-2164-15-S4-S4
- By:
- Publication type:
- Article
WS-SNPs&GO: a web server for predicting the eleterious effect of human protein variants sing functional annotation.
- Published in:
- BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S6
- By:
- Publication type:
- Article
Collective judgment predicts disease-associated ingle nucleotide variants.
- Published in:
- BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S2
- By:
- Publication type:
- Article
Thoughts from SNP-SIG 2012: future challenges in he annotation of genetic variations.
- Published in:
- 2013
- By:
- Publication type:
- Proceeding
SNP-SIG Meeting 2011: Identification and annotation of SNPs in the context of structure, function, and disease.
- Published in:
- 2012
- By:
- Publication type:
- Proceeding
Cover Picture: Hierarchical Mechanochemical Switches in Angiostatin (ChemBioChem 11/2006).
- Published in:
- ChemBioChem, 2006, v. 7, n. 11, p. 1629, doi. 10.1002/cbic.200690033
- By:
- Publication type:
- Article