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“ChromHMM: automating chromatin-state discovery and characterization”
Jason Ernst and Manolis Kellis · 1906
Earlier work this paper cites.
“Tests for linear trends in proportions and frequencies”
P. Armitage · 1955
Earlier work this paper cites.
“A tutorial on hidden Markov models and selected applications in speech recognition”
L.. Rabiner · 1989
Earlier work this paper cites.
“Hidden Markov models for speech recognition”
B.. Juang and L.. Rabiner · 1991
Earlier work this paper cites.
“Hidden Markov models in computational biology”
Anders Krogh et al · 1994
Earlier work this paper cites.
“Controlling the false discovery rate: a practical and powerful approach to multiple testing”
Yoav Benjamini and Yosef Hochberg · 1995
Earlier work this paper cites.
“Hidden Markov models for sequence analysis: extension and analysis of the basic method”
Richard Hughey and Anders Krogh · 1996
Earlier work this paper cites.
“Two methods for improving performance of a HMM and their application for gene finding”
Anders Krogh · 1997
Earlier work this paper cites.
“A hidden Markov model framework for video segmentation using audio and image features”
J.. Boreczky and L.. Wilcox · 1998
Earlier work this paper cites.
“Bayesian adaptive sequence alignment algorithms.”
J Zhu, J Liu and C Lawrence · 1998
Earlier work this paper cites.
“Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21”
N. Patil et al · 2001
Earlier work this paper cites.
“A new statistical method for haplotype reconstruction from population data”
M. Stephens, N.. Smith and P. Donnelly · 2001
Earlier work this paper cites.
“A dynamic programming algorithm for haplotype block partitioning”
K. Zhang et al · 2002
Earlier work this paper cites.
“Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms”
Z.. Qin, T. Niu and J.. Liu · 2002
Earlier work this paper cites.
“Statistical significance for genomewide studies” 12883005[pmid]
John. Storey and Robert Tibshirani · 2003
Earlier work this paper cites.
“False discovery rate in linkage and association genome screens for complex disorders.” 12807801[pmid]
Chiara Sabatti, Susan Service and Nelson Freimer · 2003
Earlier work this paper cites.
“Haplotype blocks and linkage disequilibrium in the human genome”
Jeffrey. Wall and Jonathan. Pritchard · 2003
Earlier work this paper cites.
“Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies.” 12930761[pmid]
Daniel Falush, Matthew Stephens and Jonathan. Pritchard · 2003
Earlier work this paper cites.
“Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data”
Na Li and Matthew Stephens · 2003
Earlier work this paper cites.
“HMM sampling and applications to gene finding and alternative splicing”
Simon. Cawley and Lior Pachter · 2003
Earlier work this paper cites.
“Epistasis: too often neglected in complex trait studies?”
Orjan Carlborg and Chris. Haley · 2004
Earlier work this paper cites.
“False Discovery Control for Random Fields”
M. Pacifico, C. Genovese, I. Verdinelli and L. Wasserman · 2004
Cited alongside, same era.
“Identifying SNPs predictive of phenotype using random forests”
Alexandre Bureau et al · 2005
Cited alongside, same era.
“Reconstructing genetic ancestry blocks in admixed individuals”
H. Tang et al · 2006
Cited alongside, same era.
“A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase” 43035[PII]
Paul Scheet and Matthew Stephens · 2006
Cited alongside, same era.
“On model selection consistency of Lasso”
Peng Zhao and Bin Yu · 2006
Cited alongside, same era.
“Principal components analysis corrects for stratification in genome-wide association studies”
Alkes. Price et al · 2006
“MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes” 21058334[pmid]
Yun Li et al · 2010
Later among the works it cites.
“Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci”
Andre Franke et al · 2010
Later among the works it cites.
“Inference of human population history from individual whole-genome sequences”
Heng Li and Richard Durbin · 2011
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“Haplotype phasing: existing methods and new developments”
Sharon. Browning and Brian. Browning · 2011
Later among the works it cites.
“The Bayesian lasso for genome-wide association studies” 21156729[pmid]
Jiahan Li et al · 2011
Later among the works it cites.
“Bayesian variable selection regression for genome-wide association studies and other large-scale problems”
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Cited alongside, same era.
“PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data”
K. Wang et al · 2007
Cited alongside, same era.
“A new multipoint method for genome-wide association studies by imputation of genotypes”
Jonathan Marchini et al · 2007
Cited alongside, same era.
“Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering” 17924348[pmid]
Sharon?R? Browning and Brian?L? Browning · 2007
Cited alongside, same era.
“Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls”
WTCCC · 2007
Cited alongside, same era.
“Practical issues in imputation-based association mapping”
Yongtao Guan and Matthew Stephens · 2008
Cited alongside, same era.
“Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies”
Clive. Hoggart, John. Whittaker, Maria De and David. Balding · 2008
Cited alongside, same era.
Yongtao Guan and Matthew Stephens · 2011
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“Stability selection for genome-wide association”
David. Alexander and Kenneth Lange · 2011
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“False discovery rate for scanning statistics”
D.. Siegmund, N.. Zhang and B. Yakir · 2011
Later among the works it cites.
“The mystery of missing heritability: Genetic interactions create phantom heritability” 22223662[pmid]
Or Zuk, Eliana Hechter, Shamil. Sunyaev and Eric. Lander · 2012
Later among the works it cites.
“Discovery and refinement of loci associated with lipid levels” Article
Global Consortium · 2013
Later among the works it cites.
“On asymptotically optimal confidence regions and tests for high-dimensional models”
Sara van Geer, Peter Bühlmann, Ya’acov Ritov and Ruben Dezeure · 2014
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“Defining the role of common variation in the genomic and biological architecture of adult human height” Article
Andrew. Wood et al · 2014
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“Estimation and inference of heterogeneous treatment effects using random forests”
S. Wager and S. Athey · 2015
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“Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations” Article
Jimmy. Liu et al · 2015
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“Panning for gold: model-free knockoffs for high-dimensional controlled variable selection”
E. Candes, Y. Fan, L. Janson and J. Lv · 2016
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“A knockoff filter for high-dimensional selective inference”
R. Foygel Barber and E.. Candes · 2016
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“The knockoff filter for FDR control in group-sparse and multitask regression”
Ran Dai and Rina Barber · 2016
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“Controlling the rate of GWAS false discoveries” 27784720[pmid]
Damian Brzyski et al · 2017
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“Rare and low-frequency coding variants alter human adult height” Article
Eirini Marouli et al · 2017
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“Controlling the false discovery rate via knockoffs”
Rina Barber and Emmanuel. Candès · 2085
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