about
DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disordersVirtual Pharmacist: A Platform for PharmacogenomicsFrom Molecules to Patients: The Clinical Applications of Translational BioinformaticsIntegrative visual analysis of protein sequence mutations.INPS: predicting the impact of non-synonymous variations on protein stability from sequence.In silico comparative characterization of pharmacogenomic missense variants.Non-synonymous variations in cancer and their effects on the human proteome: workflow for NGS data biocuration and proteome-wide analysis of TCGA data.A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE)Collective judgment predicts disease-associated single nucleotide variantsVariBench: a benchmark database for variations.Variation Interpretation Predictors: Principles, Types, Performance, and Choice.tmVar: a text mining approach for extracting sequence variants in biomedical literature.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.SIFT Indel: predictions for the functional effects of amino acid insertions/deletions in proteinsPaPI: pseudo amino acid composition to score human protein-coding variants.Computational methods and resources for the interpretation of genomic variants in cancerIncorporating molecular and functional context into the analysis and prioritization of human variants associated with cancerDiMeX: A Text Mining System for Mutation-Disease Association Extraction.Bioinformatics and variability in drug response: a protein structural perspective.PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions.VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics.Bioinformatics Methods and Tools to Advance Clinical Care. Findings from the Yearbook 2015 Section on Bioinformatics and Translational InformaticsCurrent and emerging technology approaches in genomicsAssessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel).PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations.Blind prediction of deleterious amino acid variations with SNPs&GO.PhD-SNPg: a webserver and lightweight tool for scoring single nucleotide variants.Tools for Predicting the Functional Impact of Nonsynonymous Genetic Variation.Protein function in precision medicine: deep understanding with machine learning.DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach.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.GABBR1 has a HERV-W LTR in its regulatory region--a possible implication for schizophrenia.
P2860
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P2860
description
2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2012
@ast
im Juli 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: July 2012)
@en
vedecký článok (publikovaný 2012-07)
@sk
vědecký článek publikovaný v roce 2012
@cs
wetenschappelijk artikel (gepubliceerd in 2012-07)
@nl
наукова стаття, опублікована в липні 2012
@uk
مقالة علمية (نشرت في يوليو 2012)
@ar
name
Bioinformatics for personal genome interpretation
@ast
Bioinformatics for personal genome interpretation
@en
Bioinformatics for personal genome interpretation
@nl
type
label
Bioinformatics for personal genome interpretation
@ast
Bioinformatics for personal genome interpretation
@en
Bioinformatics for personal genome interpretation
@nl
prefLabel
Bioinformatics for personal genome interpretation
@ast
Bioinformatics for personal genome interpretation
@en
Bioinformatics for personal genome interpretation
@nl
P2860
P3181
P356
P1476
Bioinformatics for personal genome interpretation
@en
P2093
Maricel G Kann
Nathan L Nehrt
P2860
P304
P3181
P356
10.1093/BIB/BBR070
P407
P577
2012-07-01T00:00:00Z