EXPERIMENTAL-DESIGN AND ERROR-DETECTION FOR POLYPLOID RADIATION HYBRID MAPPING

Citation
Kl. Lunetta et al., EXPERIMENTAL-DESIGN AND ERROR-DETECTION FOR POLYPLOID RADIATION HYBRID MAPPING, PCR methods and applications, 5(2), 1995, pp. 151-163
Citations number
21
Categorie Soggetti
Biothechnology & Applied Migrobiology",Biology
ISSN journal
10549803
Volume
5
Issue
2
Year of publication
1995
Pages
151 - 163
Database
ISI
SICI code
1054-9803(1995)5:2<151:EAEFPR>2.0.ZU;2-M
Abstract
In this paper we consider issues of experimental design and error dete ction and correction for polyploid radiation hybrid mapping. Using ana lytic methods and computer simulation, we first consider the combinati ons of fragment retention rate, ploidy, and marker spacing that provid e the best chance to order markers. We find that in general, combinati ons of ploidy and chromosome-specific retention rates that lead to a p er-hybrid retention rate of similar to 50% result in the greatest powe r to order markers. We also find that analyzing polyploid radiation hy brids as if they were haploid does not compromise the ability to order markers but does result in less accurate intermarker distance estimat es. Second, we examine the effect of typing errors on two-locus inform ation, ability to order multiple loci, and estimation of intermarker d istances and total map length. Even low levels of error result in larg e losses of information about breakage probabilities, markedly reduce ability to order loci, and inflate estimates of intermarker distances and total map length. We compare the ordering accuracy that results fr om duplicate typing of hybrids to that of single typing twice as many hybrids and find that duplicate typing resuts in a higher probability of identifying the true order as one of the best orders, but that sing le typing of twice as many hybrids results in stronger support for the true order. For low error rates, framework maps constructed from the larger single-typed panels are only slightly less likely to be correct and include substantially more markers than the smaller double-typed panels. Third, we develop a method to calculate the distribution of th e number of obligate chromosome breaks for a polyploid radiation hybri d under a given locus order and discuss how this method may be used to identify hybrids with suspiciously large numbers of chromosome breaks .