SuSPect: enhanced prediction of single amino acid variant (SAV) phenotype using network features
about
Genomic Characterization of the Genus Nairovirus (Family Bunyaviridae)Analysis of genetic variation and potential applications in genome-scale metabolic modelingThe 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2AThe Phyre2 web portal for protein modeling, prediction and analysisDeciphering the impact of somatic mutations in exon 20 and exon 9 of PIK3CA gene in breast tumors among Indian women through molecular dynamics approach.Structure prediction and analysis of neuraminidase sequence variants.PinSnps: structural and functional analysis of SNPs in the context of protein interaction networksBiological function derived from predicted structures in CASP11.Three-Dimensional Model of Human Nicotinamide Nucleotide Transhydrogenase (NNT) and Sequence-Structure Analysis of its Disease-Causing Variations.Molecular Determinants of Mutant Phenotypes, Inferred from Saturation Mutagenesis DataSingle nucleotide variations: biological impact and theoretical interpretation.X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 geneSystematic Mapping of Protein Mutational Space by Prolonged Drift Reveals the Deleterious Effects of Seemingly Neutral MutationsENTPRISE: An Algorithm for Predicting Human Disease-Associated Amino Acid Substitutions from Sequence Entropy and Predicted Protein StructuresExploring the cellular basis of human disease through a large-scale mapping of deleterious genes to cell typesThe structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants.Germline mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.Alpha Helices Are More Robust to Mutations than Beta StrandsAccurate prediction of functional effects for variants by combining gradient tree boosting with optimal neighborhood properties.aura (mid1ip1l) regulates the cytoskeleton at the zebrafish egg-to-embryo transition.Computational assessment of feature combinations for pathogenic variant prediction.Associating mutations causing cystinuria with disease severity with the aim of providing precision medicine.Predicting phenotype from genotype: Improving accuracy through more robust experimental and computational modeling.Annotating Mutational Effects on Proteins and Protein Interactions: Designing Novel and Revisiting Existing Protocols.Functional variomics and network perturbation: connecting genotype to phenotype in cancer.PTENpred: A Designer Protein Impact Predictor for PTEN-related Disorders.Prediction of the impact of coding missense and nonsense single nucleotide polymorphisms on HD5 and HBD1 antibacterial activity against Escherichia coli.Evolutionary and functional implications of hypervariable loci within the skin virome.The Contribution of Missense Mutations in Core and Rim Residues of Protein-Protein Interfaces to Human Disease.Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia.Induced Mutagenesis in UGT74S1 Gene Leads to Stable New Flax Lines with Altered Secoisolariciresinol Diglucoside (SDG) Profiles.Anatomy of protein disorder, flexibility and disease-related mutationsMolecular evolution of herpes simplex virus 2 complete genomes: Comparison between primary and recurrent infections.The identification of protein domains that mediate functional interactions between Rab-GTPases and RabGAPs using 3D protein modeling.Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding.Systematic Identification of Machine-Learning Models Aimed to Classify Critical Residues for Protein Function from Protein Structure.Comparative analyses of putative toxin gene homologs from an Old World viper, Daboia russelii.Mapping genetic variations to three-dimensional protein structures to enhance variant interpretation: a proposed framework.Experimental determination and prediction of the fitness effects of random point mutations in the biosynthetic enzyme HisA.Prediction of protein disorder based on IUPred.
P2860
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P2860
SuSPect: enhanced prediction of single amino acid variant (SAV) phenotype using network features
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
SuSPect: enhanced prediction o ...... enotype using network features
@ast
SuSPect: enhanced prediction o ...... enotype using network features
@en
SuSPect: enhanced prediction of single amino acid variant
@nl
type
label
SuSPect: enhanced prediction o ...... enotype using network features
@ast
SuSPect: enhanced prediction o ...... enotype using network features
@en
SuSPect: enhanced prediction of single amino acid variant
@nl
prefLabel
SuSPect: enhanced prediction o ...... enotype using network features
@ast
SuSPect: enhanced prediction o ...... enotype using network features
@en
SuSPect: enhanced prediction of single amino acid variant
@nl
P2093
P2860
P1476
SuSPect: enhanced prediction o ...... enotype using network features
@en
P2093
Christopher M Yates
Ioannis Filippis
Lawrence A Kelley
P2860
P304
P356
10.1016/J.JMB.2014.04.026
P407
P577
2014-05-05T00:00:00Z