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PMID: 8476393 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A maximum-likelihood model-fitting approach to conducting a Hayman analysis of diallel tables with complete or missing data.

Behavior genetics ·Vol. 23 ·No. 1 ·1993-01-00 ·Pages 69-76

Rodriguez LA, Fulker DW, Cherny SS

Abstract

A method is presented for conducting a Hayman analysis of non-replicated diallel tables using a maximum-likelihood (ML) model-fitting approach, rather than a traditional analysis of variance (ANOVA) approach. Hayman's linear model for a diallel analysis is used to generate a table of expected cell means. This table of expected cell means is fit to a table of observed cell means, and the fit is assessed using a chi-square value. Often data collected from diallel crosses fail to meet the underlying assumptions of ANOVA. The ML method makes no assumptions about equal cell sizes or homogeneity of variance. Thus, the ML method for diallel analysis provides some statistical advantages over ANOVA methods. The ML method also offers the advantage of having the ability to analyze diallels with missing cells. Using the ML method, incomplete diallel tables can be analyzed, and the partitioning of all the sources of variation in a diallel table is still accomplished from the remaining crosses. These advantages make the ML method an attractive approach for extracting the maximum amount of information from a diallel table.

MeSH Terms
Alleles Animals Arousal/genetics Crosses, Genetic Exploratory Behavior Likelihood Functions Mice Mice, Inbred Strains Models, Genetic Motor Activity/genetics Phenotype
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rodriguez L A
Institute for Behavioral Genetics, University of Colorado, Boulder 80309-0447.
Fulker D W
Cherny S S
References (6)
6 references, click to expand
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Article Info
Journal
Behavior genetics
Abbr.
Behav Genet
ISSN
0001-8244
Published
1993-01-00
Pages
69-76
Language
English
Region
United States
NLM ID
0251711
Subset
IM
Grants
NICHD NIH HHS · HD-07289 · United States
NICHD NIH HHS · HD-21709 · United States
NCRR NIH HHS · RR-07013-25 · United States
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