标题
Blind prediction of deleterious amino acid variations with SNPs&GO
作者
关键词
-
出版物
HUMAN MUTATION
Volume 38, Issue 9, Pages 1064-1071
出版商
Wiley
发表日期
2017-01-20
DOI
10.1002/humu.23179
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- VarI-SIG 2015: methods for personalized medicine – the role of variant interpretation in research and diagnostics
- (2016) Yana Bromberg et al. BMC GENOMICS
- Variation Interpretation Predictors: Principles, Types, Performance, and Choice
- (2016) Abhishek Niroula et al. HUMAN MUTATION
- Crowdsourcing biomedical research: leveraging communities as innovation engines
- (2016) Julio Saez-Rodriguez et al. NATURE REVIEWS GENETICS
- An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
- (2014) Catherine A Brownstein et al. GENOME BIOLOGY
- WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation
- (2013) Emidio Capriotti et al. BMC GENOMICS
- The Cancer Genome Atlas Pan-Cancer analysis project
- (2013) John N Weinstein et al. NATURE GENETICS
- How to evaluate performance of prediction methods? Measures and their interpretation in variation effect analysis
- (2012) Mauno Vihinen BMC GENOMICS
- Bioinformatics for personal genome interpretation
- (2012) E. Capriotti et al. BRIEFINGS IN BIOINFORMATICS
- Guidelines for Reporting and Using Prediction Tools for Genetic Variation Analysis
- (2012) Mauno Vihinen HUMAN MUTATION
- Bioinformatics challenges for personalized medicine
- (2011) Guy Haskin Fernald et al. BIOINFORMATICS
- A new disease-specific machine learning approach for the prediction of cancer-causing missense variants
- (2011) Emidio Capriotti et al. GENOMICS
- Exploring the functional consequences of genomic variation: The 2010 Human Genome Variation Society Scientific Meeting
- (2011) William S. Oetting HUMAN MUTATION
- Performance of mutation pathogenicity prediction methods on missense variants
- (2011) Janita Thusberg et al. HUMAN MUTATION
- Easy retrieval of single amino-acid polymorphisms and phenotype information using SwissVar
- (2010) Anaïs Mottaz et al. BIOINFORMATICS
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- International network of cancer genome projects
- (2010) Thomas J. Hudson (Chairperson) et al. NATURE
- Automated inference of molecular mechanisms of disease from amino acid substitutions
- (2009) B. Li et al. BIOINFORMATICS
- Functional annotations improve the predictive score of human disease-related mutations in proteins
- (2009) Remo Calabrese et al. HUMAN MUTATION
- Distance-scaled, finite ideal-gas reference state improves structure-derived potentials of mean force for structure selection and stability prediction
- (2002) Hongyi Zhou et al. PROTEIN SCIENCE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search