DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indels
出版年份 2013 全文链接
标题
DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indels
作者
关键词
Support Vector Machine, Relative Entropy, Support Vector Machine Model, Accessible Surface Area, Matthews Correlation Coefficient
出版物
GENOME BIOLOGY
Volume 14, Issue 3, Pages R23
出版商
Springer Nature
发表日期
2013-03-13
DOI
10.1186/gb-2013-14-3-r23
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。- Quantifying harmful mutations in human populations
- (2012) Sankar Subramanian EUROPEAN JOURNAL OF HUMAN GENETICS
- 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data
- (2012) Jie Huang et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Evolutionary diagnosis method for variants in personal exomes
- (2012) Sudhir Kumar et al. NATURE METHODS
- The 1000 Genomes Project: data management and community access
- (2012) Laura Clarke et al. NATURE METHODS
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- Predicting the effects of frameshifting indels
- (2012) Jing Hu et al. GENOME BIOLOGY
- Ranking insertion, deletion and nonsense mutations based on their effect on genetic information
- (2011) Amin Zia et al. BMC BIOINFORMATICS
- Clan Genomics and the Complex Architecture of Human Disease
- (2011) James R. Lupski et al. CELL
- Functional Non-Synonymous Polymorphisms Prediction Methods: Current Approaches and Future Developments
- (2011) M. Gonzalez-Castejon et al. CURRENT MEDICINAL CHEMISTRY
- In silico SNP analysis and bioinformatics tools: a review of the state of the art to aid drug discovery
- (2011) James T.L. Mah et al. DRUG DISCOVERY TODAY
- Natural genetic variation caused by small insertions and deletions in the human genome
- (2011) R. E. Mills et al. GENOME RESEARCH
- Performance of mutation pathogenicity prediction methods on missense variants
- (2011) Janita Thusberg et al. HUMAN MUTATION
- Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data
- (2011) Gregory M. Cooper et al. NATURE REVIEWS GENETICS
- Proteome-wide evidence for enhanced positive Darwinian selection within intrinsically disordered regions in proteins
- (2011) Johan Nilsson et al. GENOME BIOLOGY
- The functional spectrum of low-frequency coding variation
- (2011) Gabor T Marth et al. GENOME BIOLOGY
- Evolutionary evidence of the effect of rare variants on disease etiology
- (2010) IP Gorlov et al. CLINICAL GENETICS
- Small insertions and deletions (INDELs) in human genomes
- (2010) J. M. Mullaney et al. HUMAN MOLECULAR GENETICS
- In silico functional profiling of human disease-associated and polymorphic amino acid substitutions
- (2010) Matthew Mort et al. HUMAN MUTATION
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Improving computational protein design by using structure-derived sequence profile
- (2010) Liang Dai et al. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
- Automated inference of molecular mechanisms of disease from amino acid substitutions
- (2009) B. Li et al. BIOINFORMATICS
- Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletions
- (2009) E. M. Kvikstad et al. GENOME RESEARCH
- Identification of deleterious non-synonymous single nucleotide polymorphisms using sequence-derived information
- (2008) Jing Hu et al. BMC BIOINFORMATICS
- Improving the prediction accuracy of residue solvent accessibility and real-value backbone torsion angles of proteins by guided-learning through a two-layer neural network
- (2008) Eshel Faraggi et al. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
- Sequence context affects the rate of short insertions and deletions in flies and primates
- (2008) Amos Tanay et al. GENOME BIOLOGY
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