Literature DB >> 22865126

A fast expectation-maximum algorithm for fine-scale QTL mapping.

Ming Fang1.   

Abstract

The recent technology of the single-nucleotide-polymorphism (SNP) array makes it possible to genotype millions of SNP markers on genome, which in turn requires to develop fast and efficient method for fine-scale quantitative trait loci (QTL) mapping. The single-marker association (SMA) is the simplest method for fine-scale QTL mapping, but it usually shows many false-positive signals and has low QTL-detection power. Compared with SMA, the haplotype-based method of Meuwissen and Goddard who assume QTL effect to be random and estimate variance components (VC) with identity-by-descent (IBD) matrices that inferred from unknown historic population is more powerful for fine-scale QTL mapping; furthermore, their method also tends to show continuous QTL-detection profile to diminish many false-positive signals. However, as we know, the variance component estimation is usually very time consuming and difficult to converge. Thus, an extremely fast EMF (Expectation-Maximization algorithm under Fixed effect model) is proposed in this research, which assumes a biallelic QTL and uses an expectation-maximization (EM) algorithm to solve model effects. The results of simulation experiments showed that (1) EMF was computationally much faster than VC method; (2) EMF and VC performed similarly in QTL detection power and parameter estimations, and both outperformed the paired-marker analysis and SMA. However, the power of EMF would be lower than that of VC if the QTL was multiallelic.

Mesh:

Year:  2012        PMID: 22865126     DOI: 10.1007/s00122-012-1949-9

Source DB:  PubMed          Journal:  Theor Appl Genet        ISSN: 0040-5752            Impact factor:   5.699


  22 in total

1.  Fine mapping of quantitative trait loci using linkage disequilibria with closely linked marker loci.

Authors:  T H Meuwissen; M E Goddard
Journal:  Genetics       Date:  2000-05       Impact factor: 4.562

2.  Fine mapping of complex trait genes combining pedigree and linkage disequilibrium information: a Bayesian unified framework.

Authors:  Miguel Pérez-Enciso
Journal:  Genetics       Date:  2003-04       Impact factor: 4.562

Review 3.  Genome-wide association studies: theoretical and practical concerns.

Authors:  William Y S Wang; Bryan J Barratt; David G Clayton; John A Todd
Journal:  Nat Rev Genet       Date:  2005-02       Impact factor: 53.242

4.  Simultaneous fine mapping of multiple closely linked quantitative trait Loci using combined linkage disequilibrium and linkage with a general pedigree.

Authors:  S H Lee; J H J Van der Werf
Journal:  Genetics       Date:  2006-06-04       Impact factor: 4.562

5.  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

6.  A new multipoint method for genome-wide association studies by imputation of genotypes.

Authors:  Jonathan Marchini; Bryan Howie; Simon Myers; Gil McVean; Peter Donnelly
Journal:  Nat Genet       Date:  2007-06-17       Impact factor: 38.330

7.  Multipoint identity-by-descent prediction using dense markers to map quantitative trait loci and estimate effective population size.

Authors:  Theo H E Meuwissen; Mike E Goddard
Journal:  Genetics       Date:  2007-06-11       Impact factor: 4.562

8.  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

9.  Likelihood methods for locating disease genes in nonequilibrium populations.

Authors:  N L Kaplan; W G Hill; B S Weir
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

10.  A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci.

Authors:  J D Terwilliger
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

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  1 in total

1.  Use of diplotypes - matched haplotype pairs from homologous chromosomes - in gene-disease association studies.

Authors:  Lingjun Zuo; Kesheng Wang; Xingguang Luo
Journal:  Shanghai Arch Psychiatry       Date:  2014-06
  1 in total

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