An exact, unifying framework for region-based association testing in family-based designs, including higher criticism approaches, SKATs, multivariate and burden tests
暂无分享,去创建一个
Scott T. Weiss | Christoph Lange | Michael H. Cho | Nan M. Laird | Julian Hecker | Jessica Lasky-Su | F. W. Townes | Priyadarshini Kachroo | John Ziniti | N. Laird | M. Cho | C. Lange | J. Ziniti | J. Lasky-Su | J. Hecker | P. Kachroo | S. Weiss
[1] Iuliana Ionita-Laza,et al. Rare Variant Analysis for Family-Based Design , 2013, PloS one.
[2] Christoph Lange,et al. A multivariate family-based association test using generalized estimating equations: FBAT-GEE. , 2003, Biostatistics.
[3] Suzanne M. Leal,et al. The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data. , 2017, American journal of human genetics.
[4] Wei Chen,et al. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis , 2015, Bioinform..
[5] S. Leal,et al. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. , 2008, American journal of human genetics.
[6] Iuliana Ionita-Laza,et al. A genome-wide scan statistic framework for whole-genome sequence data analysis , 2019, Nature Communications.
[7] Iuliana Ionita-Laza,et al. Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. , 2007, American journal of human genetics.
[8] Wei-Min Chen,et al. A generalized family-based association test for dichotomous traits. , 2009, American journal of human genetics.
[9] D. Donoho,et al. Higher criticism for detecting sparse heterogeneous mixtures , 2004, math/0410072.
[10] Xihong Lin,et al. The Generalized Higher Criticism for Testing SNP-Set Effects in Genetic Association Studies , 2017, Journal of the American Statistical Association.
[11] Scott T. Weiss,et al. A New Powerful Non-Parametric Two-Stage Approach for Testing Multiple Phenotypes in Family-Based Association Studies , 2003, Human Heredity.
[12] Xin Xu,et al. Family‐based tests for associating haplotypes with general phenotype data: Application to asthma genetics , 2004, Genetic epidemiology.
[13] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[14] Xin Xu,et al. A new multimarker test for family‐based association studies , 2007, Genetic epidemiology.
[15] Xihong Lin,et al. HYPOTHESIS TESTING FOR HIGH-DIMENSIONAL SPARSE BINARY REGRESSION. , 2013, Annals of statistics.
[16] W. Ewens,et al. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.
[17] Ingo Ruczinski,et al. A flexible and nearly optimal sequential testing approach to randomized testing: QUICK‐STOP , 2019, Genetic epidemiology.
[18] Scott T. Weiss,et al. On the Analysis of Genome-Wide Association Studies in Family-Based Designs: A Universal, Robust Analysis Approach and an Application to Four Genome-Wide Association Studies , 2009, PLoS genetics.
[19] Wei Zhou,et al. Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts , 2019, Nature Genetics.
[20] Xihong Lin,et al. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[21] Scott T. Weiss,et al. Screening and Replication using the Same Data Set: Testing Strategies for Family-Based Studies in which All Probands Are Affected , 2008, PLoS genetics.
[22] Gao T. Wang,et al. Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data. , 2017, American journal of human genetics.
[23] Jay Shendure,et al. Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data. , 2014, American journal of human genetics.
[24] Christoph Lange,et al. Family‐based association tests for survival and times‐to‐onset analysis , 2004, Statistics in medicine.
[25] Xin Xu,et al. EFBAT: exact family-based association tests , 2007, BMC Genetics.
[26] Iuliana Ionita-Laza,et al. Family-based association tests for sequence data, and comparisons with population-based association tests , 2013, European Journal of Human Genetics.
[27] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[28] Christoph Lange,et al. A comparison of popular TDT‐generalizations for family‐based association analysis , 2019, Genetic epidemiology.
[29] Christoph Lange,et al. On the association analysis of genome‐sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows , 2017, Genetic epidemiology.
[30] Christoph Lange,et al. Family‐based tests for associating haplotypes with general phenotype data , 2018, Genetic epidemiology.
[31] P. Sachs,et al. SMARCAD1 ATPase activity is required to silence endogenous retroviruses in embryonic stem cells , 2019, Nature Communications.
[32] Daniel Rabinowitz,et al. A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information , 2000, Human Heredity.
[33] N. Laird,et al. Family-based designs in the age of large-scale gene-association studies , 2006, Nature Reviews Genetics.
[34] Christoph Lange,et al. New Powerful Approaches for Family‐based Association Tests with Longitudinal Measurements , 2009, Annals of human genetics.
[35] Christoph Lange,et al. Genomic screening and replication using the same data set in family-based association testing , 2005, Nature Genetics.