Home LiteratureArticle Details
PMID: 15781700 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Quantitative trait locus study design from an information perspective.

Genetics ·Vol. 170 ·No. 1 ·2005-05-00 ·Pages 447-64

Sen S, Satagopan JM, Churchill GA

Abstract

We examine the efficiency of different genotyping and phenotyping strategies in inbred line crosses from an information perspective. This provides a mathematical framework for the statistical aspects of QTL experimental design, while guiding our intuition. Our central result is a simple formula that quantifies the fraction of missing information of any genotyping strategy in a backcross. It includes the special case of selectively genotyping only the phenotypic extreme individuals. The formula is a function of the square of the phenotype and the uncertainty in our knowledge of the genotypes at a locus. This result is used to answer a variety of questions. First, we examine the cost-information trade-off varying the density of markers and the proportion of extreme phenotypic individuals genotyped. Then we evaluate the information content of selective phenotyping designs and the impact of measurement error in phenotyping. A simple formula quantifies the information content of any combined phenotyping and genotyping design. We extend our results to cover multigenotype crosses, such as the F(2) intercross, and multiple QTL models. We find that when the QTL effect is small, any contrast in a multigenotype cross benefits from selective genotyping in the same manner as in a backcross. The benefit remains in the presence of a second unlinked QTL with small effect (explaining <20% of the variance), but diminishes if the second QTL has a large effect. Software for performing power calculations for backcross and F(2) intercross incorporating selective genotyping and marker spacing is available from http://www.biostat.ucsf.edu/sen.

MeSH Terms
Animals Chromosome Mapping/statistics & numerical data Data Interpretation, Statistical Genotype Likelihood Functions Lod Score Mice Models, Genetic Quantitative Trait Loci Research Design
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sen Saunak
Department of Epidemiology and Biostatistics, University of California, San Francisco, 94143, USA. sen@biostat.ucsf.edu
Satagopan Jaya M
Churchill Gary A
References (19)
19 references, click to expand
  1. A bayesian approach to detect quantitative trait loci using Markov chain Monte Carlo.
    Genetics. 1996 Oct;144(2):805-16 PMID: 8889541
  2. Concordance of murine quantitative trait loci for salt-induced hypertension with rat and human loci.
    Genomics. 2001 Jan 1;71(1):70-7 PMID: 11161799
  3. Effect of within-strain sample size on QTL detection and mapping using recombinant inbred mouse strains.
    Behav Genet. 1998 Jan;28(1):29-38 PMID: 9573644
  4. Selective phenotyping for increased efficiency in genetic mapping studies.
    Genetics. 2004 Dec;168(4):2285-93 PMID: 15611192
  5. Trait-based analyses for the detection of linkage between marker loci and quantitative trait loci in crosses between inbred lines.
    Theor Appl Genet. 1987 Feb;73(4):556-62 PMID: 24241113
  6. Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.
    Genetics. 1989 Jan;121(1):185-99 PMID: 2563713
  7. Two-stage designs for gene-disease association studies.
    Biometrics. 2002 Mar;58(1):163-70 PMID: 11890312
  8. Optimum spacing of genetic markers for determining linkage between marker loci and quantitative trait loci.
    Theor Appl Genet. 1994 Oct;89(2-3):351-7 PMID: 24177853
  9. R/qtl: QTL mapping in experimental crosses.
    Bioinformatics. 2003 May 1;19(7):889-90 PMID: 12724300
  10. Extreme selection strategies in gene mapping studies of oligogenic quantitative traits do not always increase power.
    Hum Hered. 1998 Mar-Apr;48(2):97-107 PMID: 9526169
  11. Maximum likelihood analysis of quantitative trait loci under selective genotyping.
    Heredity (Edinb). 2000 May;84 ( Pt 5):525-37 PMID: 10849077
  12. A simple regression method for mapping quantitative trait loci in line crosses using flanking markers.
    Heredity (Edinb). 1992 Oct;69(4):315-24 PMID: 16718932
  13. On the differences between maximum likelihood and regression interval mapping in the analysis of quantitative trait loci.
    Genetics. 2000 Oct;156(2):855-65 PMID: 11014831
  14. The effects of selective genotyping on estimates of proportion of recombination between linked quantitative trait loci.
    Theor Appl Genet. 1996 Dec;93(8):1261-6 PMID: 24162538
  15. Selective genotyping for determination of linkage between a marker locus and a quantitative trait locus.
    Theor Appl Genet. 1992 Nov;85(2-3):353-9 PMID: 24197326
  16. A statistical framework for quantitative trait mapping.
    Genetics. 2001 Sep;159(1):371-87 PMID: 11560912
  17. Optimal two-stage genotyping in population-based association studies.
    Genet Epidemiol. 2003 Sep;25(2):149-57 PMID: 12916023
  18. High-resolution mapping of quantitative trait loci by selective recombinant genotyping.
    Genetics. 2003 Aug;164(4):1657-66 PMID: 12930769
  19. The effect of selective genotyping on QTL mapping accuracy.
    Mamm Genome. 1997 Jan;8(1):67-8 PMID: 9021156
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
2005-05-00
Epub
2005-00-21
Pages
447-64
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1449722
Subset
IM
Grants
NIGMS NIH HHS · GM070683 · United States
NIGMS NIH HHS · GM60457 · United States
NCI NIH HHS · R01 CA098438 · United States
NCI NIH HHS · CA098438 · United States
NIGMS NIH HHS · R01 GM070683 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com