Efficient whole-genome association mapping using local phylogenies for unphased genotype data
暂无分享,去创建一个
[1] 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.
[2] Hamid Pezeshk,et al. BMC Bioinformatics BioMed Central Methodology article Global haplotype partitioning for maximal associated SNP pairs , 2009 .
[3] M. De Iorio,et al. Bayesian logistic regression using a perfect phylogeny. , 2007, Biostatistics.
[4] Maria De Iorio,et al. Genetic Association Mapping via Evolution-Based Clustering of Haplotypes , 2007, PLoS genetics.
[5] Sonja W. Scholz,et al. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data , 2006, The Lancet Neurology.
[6] M. Daly,et al. Evaluating and improving power in whole-genome association studies using fixed marker sets , 2006, Nature Genetics.
[7] A. Gylfason,et al. A common variant associated with prostate cancer in European and African populations , 2006, Nature Genetics.
[8] Yufeng Wu,et al. Association Mapping of Complex Diseases with Ancestral Recombination Graphs: Models and Efficient Algorithms , 2007, RECOMB.
[9] Thomas Mailund,et al. CoaSim: A flexible environment for simulating genetic data under coalescent models , 2005, BMC Bioinformatics.
[10] I. Măndoiu,et al. Highly Scalable Genotype Phasing by Entropy Minimization , 2008, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[11] Lon R Cardon,et al. Evaluating coverage of genome-wide association studies , 2006, Nature Genetics.
[12] C. Hoggart,et al. Sequence-Level Population Simulations Over Large Genomic Regions , 2007, Genetics.
[13] Eran Halperin,et al. Haplotype reconstruction from genotype data using Imperfect Phylogeny , 2004, Bioinform..
[14] D. Clayton,et al. A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region , 2006, Nature Genetics.
[15] R. Marttila,et al. Changing epidemiology of Parkinson's disease: Predicted effects of levodopa treatment , 1979, Acta neurologica Scandinavica.
[16] R. Durbin,et al. Mapping trait loci by use of inferred ancestral recombination graphs. , 2006, American journal of human genetics.
[17] Thomas Mailund,et al. Whole genome association mapping by incompatibilities and local perfect phylogenies , 2006, BMC Bioinformatics.
[18] 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.
[19] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[20] Richard M. Karp,et al. The minimum-entropy set cover problem , 2005, Theor. Comput. Sci..
[21] D. Balding,et al. Fine mapping of disease genes via haplotype clustering , 2006, Genetic epidemiology.
[22] Dan Gusfield,et al. A Linear-Time Algorithm for the Perfect Phylogeny Haplotyping (PPH) Problem , 2005, RECOMB.
[23] Amar Mukherjee,et al. An efficient algorithm for perfect phylogeny haplotyping , 2005, 2005 IEEE Computational Systems Bioinformatics Conference (CSB'05).
[24] Hannu Toivonen,et al. TreeDT: tree pattern mining for gene mapping , 2006, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[25] Michael Doebeli,et al. Adaptive Diversification in Genes That Regulate Resource Use in Escherichia coli , 2007, PLoS genetics.
[26] H Helenius,et al. Changing epidemiology of Parkinson’s disease in southwestern Finland , 1999, Neurology.
[27] Sebastian Zöllner,et al. Coalescent-Based Association Mapping and Fine Mapping of Complex Trait Loci , 2005, Genetics.
[28] Christian Gieger,et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization , 2006, Nature Genetics.