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Using ancestry matching to combine family‐based and unrelated samples for genome‐wide association studies
Authors:Andrew Crossett  Brian P. Kent  Lambertus Klei  Steven Ringquist  Massimo Trucco  Kathryn Roeder  Bernie Devlin
Affiliation:1. Department of Statistics, Carnegie Mellon University, Pittsburgh, PA 15213, U.S.A.;2. Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, U.S.A.;3. Division of Immunogenetics, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224, U.S.A.
Abstract:We propose a method to analyze family‐based samples together with unrelated cases and controls. The method builds on the idea of matched case–control analysis using conditional logistic regression (CLR). For each trio within the family, a case (the proband) and matched pseudo‐controls are constructed, based upon the transmitted and untransmitted alleles. Unrelated controls, matched by genetic ancestry, supplement the sample of pseudo‐controls; likewise unrelated cases are also paired with genetically matched controls. Within each matched stratum, the case genotype is contrasted with control/pseudo‐control genotypes via CLR, using a method we call matched‐CLR (mCLR). Eigenanalysis of numerous SNP genotypes provides a tool for mapping genetic ancestry. The result of such an analysis can be thought of as a multidimensional map, or eigenmap, in which the relative genetic similarities and differences amongst individuals is encoded in the map. Once constructed, new individuals can be projected onto the ancestry map based on their genotypes. Successful differentiation of individuals of distinct ancestry depends on having a diverse, yet representative sample from which to construct the ancestry map. Once samples are well‐matched, mCLR yields comparable power to competing methods while ensuring excellent control over Type I error. Copyright © 2010 John Wiley & Sons, Ltd.
Keywords:conditional logistic regression  family‐based design  genome‐wide association  matched case–  control  population stratification
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