Gene hunting with hidden Markov model knockoffs
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M Sesia | C Sabatti | E J Candès | E. Candès | C. Sabatti | M. Sesia | Matteo Sesia
[1] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[2] D. Haussler,et al. Hidden Markov models in computational biology. Applications to protein modeling. , 1993, Journal of molecular biology.
[3] Peng Zhao,et al. On Model Selection Consistency of Lasso , 2006, J. Mach. Learn. Res..
[4] Laurent Duret,et al. The Impact of Recombination on Nucleotide Substitutions in the Human Genome , 2008, PLoS genetics.
[5] M. Stephens,et al. Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. , 2003, Genetics.
[6] E. Lander,et al. The mystery of missing heritability: Genetic interactions create phantom heritability , 2012, Proceedings of the National Academy of Sciences.
[7] S. P. Fodor,et al. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.
[8] Marcelo P. Segura-Lepe,et al. Rare and low-frequency coding variants alter human adult height , 2016, Nature.
[9] E. Candès,et al. Controlling the false discovery rate via knockoffs , 2014, 1404.5609.
[10] J. Marchini,et al. Genotype imputation for genome-wide association studies , 2010, Nature Reviews Genetics.
[11] M. Stephens,et al. Bayesian variable selection regression for genome-wide association studies and other large-scale problems , 2011, 1110.6019.
[12] M. Stephens,et al. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. , 2003, Genetics.
[13] Tariq Ahmad,et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci , 2010, Nature Genetics.
[14] C. Hoggart,et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population , 2008, Nature Genetics.
[15] Lucas Janson,et al. Panning for gold: ‘model‐X’ knockoffs for high dimensional controlled variable selection , 2016, 1610.02351.
[16] Anders Krogh,et al. Hidden Markov models for sequence analysis: extension and analysis of the basic method , 1996, Comput. Appl. Biosci..
[17] P. Elliott,et al. UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age , 2015, PLoS medicine.
[18] P. Donnelly,et al. A new multipoint method for genome-wide association studies by imputation of genotypes , 2007, Nature Genetics.
[19] John D. Storey,et al. Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[20] Paul Scheet,et al. A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. , 2006, American journal of human genetics.
[21] Kenneth Lange,et al. Stability selection for genome‐wide association , 2011, Genetic epidemiology.
[22] Eleazar Eskin,et al. Identifying Causal Variants at Loci with Multiple Signals of Association , 2014, Genetics.
[23] S. Geer,et al. On asymptotically optimal confidence regions and tests for high-dimensional models , 2013, 1303.0518.
[24] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[25] Wenguang Sun,et al. Large‐scale multiple testing under dependence , 2009 .
[26] B. Browning,et al. Haplotype phasing: existing methods and new developments , 2011, Nature Reviews Genetics.
[27] M. Waterman,et al. A dynamic programming algorithm for haplotype block partitioning , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[28] P. Donnelly,et al. A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.
[29] N. Risch,et al. Reconstructing genetic ancestry blocks in admixed individuals. , 2006, American journal of human genetics.
[30] Ross M. Fraser,et al. Defining the role of common variation in the genomic and biological architecture of adult human height , 2014, Nature Genetics.
[31] Trevor J. Hastie,et al. Genome-wide association analysis by lasso penalized logistic regression , 2009, Bioinform..
[32] Chris S. Haley,et al. Epistasis: too often neglected in complex trait studies? , 2004, Nature Reviews Genetics.
[33] P. Donnelly,et al. Inference of population structure using multilocus genotype data. , 2000, Genetics.
[34] Eun Yong Kang,et al. Identifying Causal Variants at Loci with Multiple Signals of Association , 2014, Genetics.
[35] Tanya M. Teslovich,et al. Discovery and refinement of loci associated with lipid levels , 2013, Nature Genetics.
[36] Yongtao Guan,et al. Practical Issues in Imputation-Based Association Mapping , 2008, PLoS genetics.
[37] J. Wall,et al. Haplotype blocks and linkage disequilibrium in the human genome , 2003, Nature Reviews Genetics.
[38] Joseph T. Glessner,et al. SNP genotyping data high-resolution copy number variation detection in whole-genome PennCNV : An integrated hidden Markov model designed for Material Supplemental , 2007 .
[39] Kai Wang,et al. Multiple testing in genome-wide association studies via hidden Markov models , 2009, Bioinform..
[40] G. Abecasis,et al. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes , 2010, Genetic epidemiology.
[41] Ran Dai,et al. The knockoff filter for FDR control in group-sparse and multitask regression , 2016, ICML.
[42] P. Armitage. Tests for Linear Trends in Proportions and Frequencies , 1955 .
[43] B. Browning,et al. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. , 2007, American journal of human genetics.
[44] K. Sirotkin,et al. The NCBI dbGaP database of genotypes and phenotypes , 2007, Nature Genetics.
[45] E. Candès,et al. Near-ideal model selection by ℓ1 minimization , 2008, 0801.0345.
[46] Manolis Kellis,et al. ChromHMM: automating chromatin-state discovery and characterization , 2012, Nature Methods.
[47] John S. Boreczky,et al. A hidden Markov model framework for video segmentation using audio and image features , 1998, Proceedings of the 1998 IEEE International Conference on Acoustics, Speech and Signal Processing, ICASSP '98 (Cat. No.98CH36181).
[48] Stefan Wager,et al. Estimation and Inference of Heterogeneous Treatment Effects using Random Forests , 2015, Journal of the American Statistical Association.
[49] C. Hoggart,et al. Simultaneous Analysis of All SNPs in Genome-Wide and Re-Sequencing Association Studies , 2008, PLoS genetics.
[50] R. Durbin,et al. Inference of human population history from individual whole-genome sequences. , 2011, Nature.
[51] Anders Krogh,et al. Two Methods for Improving Performance of a HMM and their Application for Gene Finding , 1997, ISMB.
[52] Christine B. Peterson,et al. Controlling the Rate of GWAS False Discoveries , 2016, Genetics.
[53] K. Lunetta,et al. Identifying SNPs predictive of phenotype using random forests , 2005, Genetic epidemiology.
[54] Guifang Fu,et al. The Bayesian lasso for genome-wide association studies , 2011, Bioinform..
[55] Zhaohui S. Qin,et al. Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms. , 2002, American journal of human genetics.
[56] I. Verdinelli,et al. False Discovery Control for Random Fields , 2004 .
[57] Biing-Hwang Juang,et al. Hidden Markov Models for Speech Recognition , 1991 .
[58] Chiara Sabatti. Advances in Statistical Bioinformatics: Multivariate Linear Models for GWAS , 2013 .
[59] 9 Multivariate linear models for GWAS , 2022 .
[60] Chiara Sabatti,et al. False discovery rate in linkage and association genome screens for complex disorders. , 2003, Genetics.
[61] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.