Statistical Methods of SNP Data Analysis and Applications
暂无分享,去创建一个
Alexander Bulinski | Victor Sadovnichy | Oleg Butkovsky | Alexey Shashkin | Pavel Yaskov | Alexander V. Balatskiy | L. M. Samokhodskaya | Vsevolod A. Tkachuk | P. Yaskov | O. Butkovsky | V. Tkachuk | A. Bulinski | A. Shashkin | L. Samokhodskaya | V. Sadovnichy | A. Balatskiy
[1] H. Firth,et al. Comprar Oxford Handbook of Genetics | Guy Bradley-Smith | 9780199545360 | Oxford University Press , 2009 .
[2] Nitesh V. Chawla,et al. Data Mining for Imbalanced Datasets: An Overview , 2005, The Data Mining and Knowledge Discovery Handbook.
[3] Zhi-Hua Zhou,et al. Exploratory Under-Sampling for Class-Imbalance Learning , 2006, Sixth International Conference on Data Mining (ICDM'06).
[4] Scott M. Williams,et al. A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction , 2007, Genetic epidemiology.
[5] Holger Schwender,et al. Identification of SNP interactions using logic regression. , 2008, Biostatistics.
[6] E. Lehmann. Testing Statistical Hypotheses , 1960 .
[7] T. Hansen,et al. A Bayesian Multilocus Association Method: Allowing for Higher-Order Interaction in Association Studies , 2007, Genetics.
[8] T. Ogihara,et al. Identification of Hypertension-Susceptibility Genes and Pathways by a Systemic Multiple Candidate Gene Approach: The Millennium Genome Project for Hypertension , 2008, Hypertension Research.
[9] David W. Hosmer,et al. Applied Logistic Regression , 1991 .
[10] Robert Tibshirani,et al. The Elements of Statistical Learning: Data Mining, Inference, and Prediction, 2nd Edition , 2001, Springer Series in Statistics.
[11] Gérard Biau,et al. Analysis of a Random Forests Model , 2010, J. Mach. Learn. Res..
[12] Taesung Park,et al. Log-linear model-based multifactor dimensionality reduction method to detect gene-gene interactions , 2007, Bioinform..
[13] Trevor Hastie,et al. The Elements of Statistical Learning , 2001 .
[14] Alison A Motsinger,et al. The effect of reduction in cross‐validation intervals on the performance of multifactor dimensionality reduction , 2006, Genetic epidemiology.
[15] Timothy B. Stockwell,et al. The Sequence of the Human Genome , 2001, Science.
[16] J. A. Bondy,et al. Graph Theory , 2008, Graduate Texts in Mathematics.
[17] Qiang Yang,et al. MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study , 2009, BMC Bioinformatics.
[18] J. Friedman. Stochastic gradient boosting , 2002 .
[19] Achim Zeileis,et al. Bias in random forest variable importance measures: Illustrations, sources and a solution , 2007, BMC Bioinformatics.
[20] Leo Breiman,et al. Random Forests , 2001, Machine Learning.
[21] Junyong Park,et al. Independent rule in classification of multivariate binary data , 2009, J. Multivar. Anal..
[22] P. Massart,et al. Concentration inequalities and model selection , 2007 .
[23] J. H. Moore,et al. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. , 2001, American journal of human genetics.
[24] Holger Schwender,et al. Empirical Bayes Analysis of Single Nucleotide Polymorphisms Empirical Bayes Analysis of Single Nucleotide Polymorphisms , 2008 .
[25] Sayan Mukherjee,et al. Permutation Tests for Classification , 2005, COLT.
[26] Ingo Wegener,et al. Detecting high-order interactions of single nucleotide polymorphisms using genetic programming , 2007, Bioinform..
[27] Vineet Bafna,et al. RAPID detection of gene-gene interactions in genome-wide association studies , 2010, Bioinform..
[28] D. Cox. The Analysis of Multivariate Binary Data , 1972 .
[29] Samuel P. Dickson,et al. Interpretation of association signals and identification of causal variants from genome-wide association studies. , 2010, American journal of human genetics.
[30] G. Rossi,et al. Association of gene polymorphisms with coronary artery disease in low- or high-risk subjects defined by conventional risk factors. , 2004, Journal of the American College of Cardiology.
[31] Holger Schwender,et al. Testing SNPs and sets of SNPs for importance in association studies. , 2011, Biostatistics.
[32] Yan V. Sun,et al. Machine learning in genome‐wide association studies , 2009, Genetic epidemiology.
[33] J. Friedman. Greedy function approximation: A gradient boosting machine. , 2001 .
[34] Alison A. Motsinger-Reif,et al. A comparison of internal validation techniques for multifactor dimensionality reduction , 2010, BMC Bioinformatics.
[35] Sylvain Arlot,et al. A survey of cross-validation procedures for model selection , 2009, 0907.4728.
[36] Achim Zeileis,et al. BMC Bioinformatics BioMed Central Methodology article Conditional variable importance for random forests , 2008 .
[37] Nicholas L. Smith,et al. SHARE: an adaptive algorithm to select the most informative set of SNPs for candidate genetic association , 2009, Biostatistics.
[38] Kathryn A. Dowsland,et al. Simulated Annealing , 1989, Encyclopedia of GIS.
[39] Luc Devroye,et al. Consistency of Random Forests and Other Averaging Classifiers , 2008, J. Mach. Learn. Res..
[40] Jason H. Moore,et al. An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene Interactions on risk of myocardial infarction: The importance of model validation , 2004, BMC Bioinformatics.
[41] T. Rydén,et al. Fast simulated annealing in R-d with an application to maximum likelihood estimation in state-space models , 2009 .
[42] Bruce E. Hajek,et al. Cooling Schedules for Optimal Annealing , 1988, Math. Oper. Res..
[43] Arpad Kelemen,et al. Statistical advances and challenges for analyzing correlated high dimensional SNP data in genomic study for complex diseases , 2008, 0803.4065.
[44] Thomas Lumley,et al. Logic regression for analysis of the association between genetic variation in the renin-angiotensin system and myocardial infarction or stroke. , 2006, American journal of epidemiology.
[45] T. Murohara,et al. Preventive cardiology: abstractAssociation of gene polymorphisms with coronary artery disease in low- or high-risk subjects defined by conventional risk factors , 2004 .
[46] Jason H. Moore,et al. Renin-angiotensin system gene polymorphisms and coronary artery disease in a large angiographic cohort: detection of high order gene-gene interaction. , 2007, Atherosclerosis.
[47] Rachel Karchin,et al. Next generation tools for the annotation of human SNPs , 2009, Briefings Bioinform..
[48] T. Hu,et al. STRONG LAWS OF LARGE NUMBERS FOR ARRAYS OF ROWWISE INDEPENDENT RANDOM ELEMENTS , 1987 .
[49] Katja Ickstadt,et al. Comparing Logic Regression Based Methods for Identifying SNP Interactions , 2007, BIRD.