Problems with the nested granularity of feature domains in bioinformatics: the eXtasy case
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Bart De Moor | Jesse Davis | Yves Moreau | Dusan Popovic | Alejandro Sifrim | B. Moor | Y. Moreau | D. Popovic | Jesse Davis | A. Sifrim
[1] David Hinkley,et al. Bootstrap Methods: Another Look at the Jackknife , 2008 .
[2] D. Haussler,et al. Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. , 2005, Genome research.
[3] A Ziegler,et al. EDITOR Comments on ‘Practical experiences on the necessity of external validation’ , 2008 .
[4] P. Bork,et al. A method and server for predicting damaging missense mutations , 2010, Nature Methods.
[5] Insuk Lee,et al. Characterising and Predicting Haploinsufficiency in the Human Genome , 2010, PLoS genetics.
[6] P. Stankiewicz,et al. Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. , 2010, The New England journal of medicine.
[7] Leo Breiman,et al. Random Forests , 2001, Machine Learning.
[8] N. Stanietsky,et al. The interaction of TIGIT with PVR and PVRL2 inhibits human NK cell cytotoxicity , 2009, Proceedings of the National Academy of Sciences.
[9] Justin C. Fay,et al. Identification of deleterious mutations within three human genomes. , 2009, Genome research.
[10] Steven Henikoff,et al. SIFT: predicting amino acid changes that affect protein function , 2003, Nucleic Acids Res..
[11] Tom Fawcett,et al. An introduction to ROC analysis , 2006, Pattern Recognit. Lett..
[12] BMC Bioinformatics , 2005 .
[13] Fiona Cunningham,et al. A Combined Functional Annotation Score for Non-Synonymous Variants , 2012, Human Heredity.
[14] Janez Demsar,et al. Statistical Comparisons of Classifiers over Multiple Data Sets , 2006, J. Mach. Learn. Res..
[15] Bassem A. Hassan,et al. Gene prioritization through genomic data fusion , 2006, Nature Biotechnology.
[16] R. Polikar,et al. Ensemble based systems in decision making , 2006, IEEE Circuits and Systems Magazine.
[17] J. Shaffer. Multiple Hypothesis Testing , 1995 .
[18] Vanessa E. Gray,et al. Evolutionary diagnosis method for variants in personal exomes , 2012, Nature Methods.
[19] Bart De Moor,et al. eXtasy: variant prioritization by genomic data fusion , 2013, Nature Methods.
[20] Mark Goadrich,et al. The relationship between Precision-Recall and ROC curves , 2006, ICML.
[21] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[22] M. Vihinen. How to evaluate performance of prediction methods? Measures and their interpretation in variation effect analysis , 2012, BMC Genomics.
[23] Thomas G. Dietterich. Approximate Statistical Tests for Comparing Supervised Classification Learning Algorithms , 1998, Neural Computation.
[24] J.,et al. The New England Journal of Medicine , 2012 .
[25] Leo Breiman,et al. Bagging Predictors , 1996, Machine Learning.
[26] Jana Marie Schwarz,et al. MutationTaster evaluates disease-causing potential of sequence alterations , 2010, Nature Methods.
[27] Roumiana Tsenkova,et al. Near Infrared Spectroscopy Using Short Wavelengths and Leave-One-Cow-Out Cross-Validation for Quantification of Somatic Cells in Milk , 2009 .
[28] P. Stenson,et al. The Human Gene Mutation Database: 2008 update , 2009, Genome Medicine.
[29] Steven Salzberg,et al. Detection of lineage-specific evolutionary changes among primate species , 2011, BMC Bioinformatics.
[30] E. Boerwinkle,et al. dbNSFP: A Lightweight Database of Human Nonsynonymous SNPs and Their Functional Predictions , 2011, Human mutation.
[31] D. Stone,et al. Prediction of clinical drug efficacy by classification of drug-induced genomic expression profiles in vitro , 2003, Proceedings of the National Academy of Sciences of the United States of America.