Literature DB >> 33789342

Ghost QTL and hotspots in experimental crosses: novel approach for modeling polygenic effects.

Jonas Wallin1, Małgorzata Bogdan1,2, Piotr A Szulc2, R W Doerge3,4, David O Siegmund5.   

Abstract

Ghost quantitative trait loci (QTL) are the false discoveries in QTL mapping, that arise due to the "accumulation" of the polygenic effects, uniformly distributed over the genome. The locations on the chromosome that are strongly correlated with the total of the polygenic effects depend on a specific sample correlation structure determined by the genotypes at all loci. The problem is particularly severe when the same genotypes are used to study multiple QTL, e.g. using recombinant inbred lines or studying the expression QTL. In this case, the ghost QTL phenomenon can lead to false hotspots, where multiple QTL show apparent linkage to the same locus. We illustrate the problem using the classic backcross design and suggest that it can be solved by the application of the extended mixed effect model, where the random effects are allowed to have a nonzero mean. We provide formulas for estimating the thresholds for the corresponding t-test statistics and use them in the stepwise selection strategy, which allows for a simultaneous detection of several QTL. Extensive simulation studies illustrate that our approach eliminates ghost QTL/false hotspots, while preserving a high power of true QTL detection.
© The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  QTL mapping; expression quantitative trait loci (e-QTL) mapping; ghost QTL; hotspots; mixed effect model; polygenes

Mesh:

Year:  2021        PMID: 33789342      PMCID: PMC8045733          DOI: 10.1093/genetics/iyaa041

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  37 in total

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Authors:  Malgorzata Bogdan; Jayanta K Ghosh; R W Doerge
Journal:  Genetics       Date:  2004-06       Impact factor: 4.562

2.  Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations.

Authors:  Bjarke Feenstra; Ib M Skovgaard; Karl W Broman
Journal:  Genetics       Date:  2006-05-15       Impact factor: 4.562

3.  A simple regression method for mapping quantitative trait loci in line crosses using flanking markers.

Authors:  C S Haley; S A Knott
Journal:  Heredity (Edinb)       Date:  1992-10       Impact factor: 3.821

4.  Least squares interval mapping of quantitative trait loci under the infinitesimal genetic model in outbred populations.

Authors:  Z Liu; J C Dekkers
Journal:  Genetics       Date:  1998-01       Impact factor: 4.562

5.  Permutation tests for multiple loci affecting a quantitative character.

Authors:  R W Doerge; G A Churchill
Journal:  Genetics       Date:  1996-01       Impact factor: 4.562

6.  Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

Authors:  E S Lander; D Botstein
Journal:  Genetics       Date:  1989-01       Impact factor: 4.562

7.  The nature of confounding in genome-wide association studies.

Authors:  Bjarni J Vilhjálmsson; Magnus Nordborg
Journal:  Nat Rev Genet       Date:  2012-11-20       Impact factor: 53.242

8.  Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent.

Authors:  E Feingold; P O Brown; D Siegmund
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

9.  Evidence of widespread selection on standing variation in Europe at height-associated SNPs.

Authors:  Michael C Turchin; Charleston W K Chiang; Cameron D Palmer; Sriram Sankararaman; David Reich; Joel N Hirschhorn
Journal:  Nat Genet       Date:  2012-08-19       Impact factor: 38.330

10.  Genetical genomics: spotlight on QTL hotspots.

Authors:  Rainer Breitling; Yang Li; Bruno M Tesson; Jingyuan Fu; Chunlei Wu; Tim Wiltshire; Alice Gerrits; Leonid V Bystrykh; Gerald de Haan; Andrew I Su; Ritsert C Jansen
Journal:  PLoS Genet       Date:  2008-10-24       Impact factor: 5.917

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