Evaluation of algorithms used to order markers on genetic maps


Autoria(s): MOLLINARI, M.; MARGARIDO, G. R. A.; VENCOVSKY, R.; GARCIA, A. A. F.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2009

Resumo

When building genetic maps, it is necessary to choose from several marker ordering algorithms and criteria, and the choice is not always simple. In this study, we evaluate the efficiency of algorithms try (TRY), seriation (SER), rapid chain delineation (RCD), recombination counting and ordering (RECORD) and unidirectional growth (UG), as well as the criteria PARF (product of adjacent recombination fractions), SARF (sum of adjacent recombination fractions), SALOD (sum of adjacent LOD scores) and LHMC (likelihood through hidden Markov chains), used with the RIPPLE algorithm for error verification, in the construction of genetic linkage maps. A linkage map of a hypothetical diploid and monoecious plant species was simulated containing one linkage group and 21 markers with fixed distance of 3 cM between them. In all, 700 F(2) populations were randomly simulated with and 400 individuals with different combinations of dominant and co-dominant markers, as well as 10 and 20% of missing data. The simulations showed that, in the presence of co-dominant markers only, any combination of algorithm and criteria may be used, even for a reduced population size. In the case of a smaller proportion of dominant markers, any of the algorithms and criteria (except SALOD) investigated may be used. In the presence of high proportions of dominant markers and smaller samples (around 100), the probability of repulsion linkage increases between them and, in this case, use of the algorithms TRY and SER associated to RIPPLE with criterion LHMC would provide better results. Heredity (2009) 103, 494-502; doi:10.1038/hdy.2009.96; published online 29 July 2009

Conselho Nacional de Desenvolvimento Tecnologico (CNPq)[132314/2006-1]

Conselho Nacional de Desenvolvimento Tecnologico (CNPq)[308139/2007-0]

Fundacao de Amparo a Pesquisa de Sao Paulo (FAPESP)[2008/54402-4]

Fundacao de Amparo a Pesquisa de Sao Paulo (FAPESP)[2007/02775-9]

Identificador

HEREDITY, v.103, n.6, p.494-502, 2009

0018-067X

http://producao.usp.br/handle/BDPI/19165

10.1038/hdy.2009.96

http://dx.doi.org/10.1038/hdy.2009.96

Idioma(s)

eng

Publicador

NATURE PUBLISHING GROUP

Relação

Heredity

Direitos

restrictedAccess

Copyright NATURE PUBLISHING GROUP

Palavras-Chave #multipoint estimates #seriation #rapid chain delineation #recombination counting and ordering #unidirectional growth #MULTILOCUS LINKAGE ANALYSIS #QUANTITATIVE TRAIT LOCI #CONSTRUCTION #HUMANS #RECOMBINATION #GENOMICS #SORGHUM #VALUES #DART #AFLP #Ecology #Evolutionary Biology #Genetics & Heredity
Tipo

article

original article

publishedVersion