Estimation of significance thresholds for genomewide association scans
暂无分享,去创建一个
[1] N. Morton. Sequential tests for the detection of linkage. , 1955, American journal of human genetics.
[2] Z. Šidák. Rectangular Confidence Regions for the Means of Multivariate Normal Distributions , 1967 .
[3] A. Tamhane,et al. Multiple Comparison Procedures , 1989 .
[4] S. S. Young,et al. Resampling-Based Multiple Testing: Examples and Methods for p-Value Adjustment , 1993 .
[5] R. Doerge,et al. Empirical threshold values for quantitative trait mapping. , 1994, Genetics.
[6] E. Lander,et al. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.
[7] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[8] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[9] R. Gürtler,et al. Modeling Household Transmission of American Trypanosomiasis , 2001, Science.
[10] R. Tibshirani,et al. Empirical bayes methods and false discovery rates for microarrays , 2002, Genetic epidemiology.
[11] Frank Dudbridge,et al. Rank truncated product of P‐values, with application to genomewide association scans , 2003, Genetic epidemiology.
[12] K. Manly,et al. Genomics, prior probability, and statistical tests of multiple hypotheses. , 2004, Genome research.
[13] Nathaniel Rothman,et al. Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. , 2004, Journal of the National Cancer Institute.
[14] D. Clayton,et al. Betting odds and genetic associations. , 2004, Journal of the National Cancer Institute.
[15] Frank Dudbridge,et al. Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies. , 2004, American journal of human genetics.
[16] M. Olivier. A haplotype map of the human genome , 2003, Nature.
[17] M. Olivier. A haplotype map of the human genome. , 2003, Nature.
[18] J. Ioannidis. Why Most Published Research Findings Are False , 2005, PLoS medicine.
[19] H. Keselman,et al. Multiple Comparison Procedures , 2005 .
[20] D. Reich,et al. Population Structure and Eigenanalysis , 2006, PLoS genetics.
[21] M. Daly,et al. Evaluating and improving power in whole-genome association studies using fixed marker sets , 2006, Nature Genetics.
[22] Lon R Cardon,et al. Evaluating coverage of genome-wide association studies , 2006, Nature Genetics.
[23] P. Donnelly,et al. A new multipoint method for genome-wide association studies by imputation of genotypes , 2007, Nature Genetics.
[24] Jon Wakefield,et al. A Bayesian measure of the probability of false discovery in genetic epidemiology studies. , 2007, American journal of human genetics.
[25] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[26] K. Mossman. The Wellcome Trust Case Control Consortium, U.K. , 2008 .