 Methodology article
 Open Access
 Published:
Multiallelic epistatic model for an outbred cross and mapping algorithm of interactive quantitative trait loci
BMC Plant Biology volume 11, Article number: 148 (2011)
Abstract
Background
Genetic mapping has proven to be powerful for studying the genetic architecture of complex traits by characterizing a network of the underlying interacting quantitative trait loci (QTLs). Current statistical models for genetic mapping were mostly founded on the biallelic epistasis of QTLs, incapable of analyzing multiallelic QTLs and their interactions that are widespread in an outcrossing population.
Results
Here we have formulated a general framework to model and define the epistasis between multiallelic QTLs. Based on this framework, we have derived a statistical algorithm for the estimation and test of multiallelic epistasis between different QTLs in a fullsib family of outcrossing species. We used this algorithm to genomewide scan for the distribution of multiallelic epistasis for a rooting ability trait in an outbred cross derived from two heterozygous poplar trees. The results from simulation studies indicate that the positions and effects of multiallelic QTLs can well be estimated with a modest sample and heritability.
Conclusions
The model and algorithm developed provide a useful tool for better characterizing the genetic control of complex traits in a heterozygous family derived from outcrossing species, such as forest trees, and thus fill a gap that occurs in genetic mapping of this group of important but underrepresented species.
Background
Approaches for quantitative trait locus (QTL) mapping were developed originally for experimental crosses, such as the backcross, double haploid, RILs or F_{2}, derived from inbred lines [1–3]. Because of the homozygosity of inbred lines, the Mendelian (co)segregation of all markers each with two alternative alleles in such crosses can be observed directly. In practice, there is also a group of species of great economical and environmental importance  outcrossing species, such as forest trees, in which traditional QTL mapping approaches cannot be appropriately used. For these species, it is difficult or impossible to generate inbred lines due to long generation intervals and high heterozygosity [4], although experimental hybrids have been commercially used in practical breeding programs.
For a given outbred line, some markers may be heterozygous, whereas others may be homozygous over the genome. All markers may, or may not, have the same allele system between any two outbred lines used for a cross. Also, for a pair of heterozygous loci, their allelic configuration along two homologous chromosomes (i.e., linkage phase) cannot be observed from the segregation pattern of genotypes in the cross [5, 6]. Unfortunately, a consistent number of alleles across different markers and their known linkage phases are the prerequisites for statistical mapping approaches described for the backcross or F_{2}. Grattapaglia and Sederoff [7] proposed a socalled pseudotest backcross strategy for linkage mapping in a controlled cross between two outbred parents. This strategy is powerful for the linkage analysis of those testcross markers that are heterozygous in one parent and null in the other, although it fails to consider many other marker cross types, such as intercross markers and dominant markers, that occur for an outbred cross. Maliepaard et al. [8] derived numerous formulas for estimating the linkage between different types of markers by correctly determining the linkage phase of markers. A general model has been developed for simultaneous estimation of the linkage and linkage phase for any marker cross type in outcrossing populations [9, 10]. Stam [11] wrote powerful software for integrating genetic linkage maps using different types of markers.
Statistical methods for QTL mapping in a fullsib family of outcrossing species have not received adequate attention. Lin et al. [12] developed a model that takes into account uncertainties about the number of alleles across the genome. Wu et al. [13] used this model to reanalyze a fullsib family data for poplar trees [14], leading to the detection of new QTLs for biomass traits which were not discovered by traditional approaches. With increasing recognition of the role of epistasis in controlling and maintaining quantitative variation [15], it is crucial to extend Lin et al.'s model to map the epistatic of QTLs by which to elucidate a detailed and comprehensive perspective on the genetic architecture of a quantitative trait. However, the wellestablished theory and model for epistasis are mostly based on biallelic genes [16] and their estimation and test are made for a pedigree derived from inbred lines [17]. Until now, no models and algorithms have been available for characterizing the epistasis of multiallelic QTLs in an outcrossing population.
In this article, we will extend the theory for biallelic epistasis to model the epistasis between different QTLs each with multiple alleles. The multiallelic epistatic theory is then implemented into a statistical model for QTL mapping based on a mixture model. We have derived a closed form for the estimation of the main and interactive effects of multiallelic QTLs within the EM framework. Our model allows geneticists to test the effects of individual genetic components on trait variation. The estimating model has been investigated through simulation studies and validated by an example of QTL mapping for poplar trees [18]. The algorithm has been packed to a newly developed package of software, 3FunMap, derived to map QTLs in a fullsib family [19].
Quantitative Genetic Model
Additivedominance Model
Randomly select two heterozygous lines as parents P_{1} and P_{2} to produce a fullsib family, in which a QTL will form four genotypes if the two lines have completely different allele systems. Let μ_{ uv }be the value of a QTL genotype inheriting allele u (u = 1,2) from parent P_{1} and allele v (v = 3, 4) from parent P_{2}. Based on quantitative genetic theory, this genotypic value can be partitioned into the additive and dominant effects as follows:
where μ is the overall mean, α_{ u }and β_{ v }are the allelic (additive) effects of allele u and v, respectively, and γ_{ uv }is the interaction (dominant) effect at the QTL. Considering all possible alleles and allele combinations between the two parent, there are a total of four additive effects (α_{1} and α_{2} from parent P_{1} and β_{3} and β_{4} from parent P_{2} and four dominant effects (γ_{13}, γ_{14}, γ_{23} and γ_{34}). But these additive and dominant effects are not independent and, therefore, are not estimable. After parameterization, there are two independent additive effects, α = α_{1} = α_{2} and β_{3} = β_{3} = β_{4}, and one dominant effect, γ = γ_{13} = γ_{14} = γ_{23} = γ_{24}, to be estimated.
Let u = (μ_{ uv })_{4 × 1} and a = (μ, α, β, γ)^{T}, which can be connected by a design matrix D. We have
where
The expression of a can be obtained from the expression of u by
Additivedominanceepistatic Model
If there are two segregating QTL in the fullsib family, the epistatic effects due to their nonallelic interactions should be considered. The theory for epistasis in an inbred family [16] can be readily extended to specify different epistatic components for outbred crosses. Consider two epistatic multiallelic QTL, each of which has four different genotypes, 13, 14, 23, and 24, in the outbred progeny. Let ${\mu}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}}$ be the genotypic value for QTL genotype u_{1}v_{1}/u_{2}v_{2} for u_{1},u_{2} = 1,2 and v_{1},v_{2} = 3,4 and $u=\left({\mu}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}}\right)$ be the corresponding mean vector. The twoQTL genotypic value is partitioned into different components as follows:
where

(1)
μ is the overall mean;

(2)
α _{1} is the additive effect due to the substitution from allele 1 to 2 at the first QTL;

(3)
β _{1} is the additive effect due to the substitution from allele 3 to 4 at the first QTL;

(4)
γ _{1} is the dominant effect due to the interaction between alleles from different parents;

(5)
α _{2} is the additive effect due to the substitution from allele 1 to 2 at the second QTL;

(6)
β _{2} is the additive effect due to the substitution from allele 3 to 4 at the second QTL;

(7)
γ _{2} is the dominant effect due to the interaction between alleles from different parents;

(8)
I _{ αα }is the additive × additive epistatic effect due to the interaction between the substitutions from allele 1 to 2 at the first and second QTLs;

(9)
I _{ αβ }is the additive × additive epistatic effect due to the interaction between the substitutions from allele 1 to 2 at the first QTL and from allele 3 to 4 at the second QTL;

(10)
I _{ βα }is the additive × additive epistatic effect due to the interaction between the substitutions from allele 3 to 4 at the first QTL and from allele 1 to 2 at the second QTL;

(11)
I _{ αβ }is the additive × additive epistatic effect due to the interaction between the substitutions from allele 3 to 4 at the first and second QTLs;

(12)
J _{ αγ }is the additive × dominant epistatic effect due to the interaction between the substitutions from allele 1 to 2 at the first QTL and the dominant effect at the second QTL;

(13)
J _{ βγ }is the additive × dominant epistatic effect due to the interaction between the substitutions from allele 3 to 4 at the first QTL and the dominant effect at the second QTL;

(14)
K _{ γα }is the dominant × additive epistatic effect due to the interaction between the dominant effect at the first QTL and the substitutions from allele 1 to 2 at the second QTL;

(15)
K _{ γβ }is the dominant × additive epistatic effect due to the interaction between the dominant effect at the first QTL and the substitutions from allele 3 to 4 at the second QTL;

(16)
L _{ γγ }is the dominant × dominant epistatic effect due to the interaction between the dominant effects at the first and second QTLs.
Genetic effect parameters for two interacting QTL are arrayed in a = (μ, α_{1}, β_{1}, γ_{1}, α_{2}, β_{2}, γ_{2}, I_{ αα }, I_{ αβ }, I_{ βα }, I_{ ββ }, J_{ αγ }, J_{ βγ }, K_{ γα }, K_{ γβ }, L_{ γγ })^{T}. We relate the genotypic value vector and genetic effect vector by
where design matrix
Thus, the genetic effect vector can be expressed, in terms of the genotypic value vector, as
If we have alleles 1 = 3 and 2 = 4 for an outbred family, Equations 1 and 3 will be reduced to traditional biallelic additivedominant and biallelic additivedominantepistatic genetic models, respectively [20].
Statistical Model
Likelihood
Suppose there is a fullsib family of size n derived from two outbred lines. Consider two interacting QTLs for a quantitative trait. Let u_{1}v_{1} and u_{2}v_{2} denote a general genotype at QTL 1 and 2, respectively, where u_{1} and u_{2} (u_{1},u_{2} = 1,2) are the alleles inherited from parent P_{1} and v_{1} and v_{2} (v_{1},v_{2} = 3,4) are the alleles inherited from parent P_{2}. The linear model of the trait value (y_{ i }) for individual i affected by the two QTLs is written as
where ${\xi}_{i{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}}$ is the indicator variable for QTL genotypes defined as 1 if a particular genotype u_{1}v_{1}/u_{2}v_{2} is considered for individual i and 0 otherwise, and e_{ i }is the residual error normally distributed with mean 0 and variance σ^{2}. The probability with which individual i carries QTL genotype u_{1}v_{1}/u_{2}v_{2} can be inferred from its marker genotype, with this conditional probability expressed as ${\omega}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}i}$[20].
The loglikelihood of the putative QTLs given the trait value (y) and marker information (M) is given by
where Θ is the vector for unknown parameters that include the QTL position expressed by the conditional probabilities $\left({\omega}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}i}\right)$, QTL genotypic values $\left({\mu}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}}\right)$ and the residual variance (σ^{2}). The first parameters, denoted by Θ_{ p }, are contained in the mixture proportions of the above model, whereas the second two, denoted by Θ_{ q }, are quantitative genetic parameters. Normal distribution density $f{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}\left({y}_{i}\right)$ has mean ${\mu}_{{u}_{1}{v}_{1}\u2215{u}_{2}{v}_{2}}$ and variance σ^{2}.
EM Algorithm
The standard EM algorithm is developed to obtain the estimates of the unknown vector. By differentiating the loglikelihood of equation (6) with respect to two groups of unknown parameters (Θ_{ p }, Θ_{ q }), we have
where we define
which could be thought of as a posterior probability that individual i has a QTL genotype u_{1}v_{1}/u_{2}v_{2}.
In the E step, calculate the posterior probabilities of QTL genotypes given the marker genotype of individual i by equation (7). In the M step, estimate the maximum likelihood estimates (MLEs) of the unknown parameters by solving $\frac{\partial}{\partial \Theta}logL\left(\Theta y,M\right)=0.$. The closed forms for estimating the genotypic values and residual variance are derived as
By giving initial values for the parameters, the E and M steps are iterated until the estimates are stable. The stable values are the MLEs of the unknown parameters. Note that the QTL position within a marker interval can be estimated by treating the position is fixed. Using a grid search, we can obtain the MLE of the QTL position from the peak of the profile of the loglikelihood ratio test statistics across a chromosome.
Hypothesis Tests
After the parameters are estimated, a number of hypothesis tests can be made. The existence of a QTL can be tested by formulating the null hypothesis expressed as
The likelihoods under the reduced (H_{0}) and full model (H_{1}) are calculated and their loglikelihood ratio (LR) is then estimated by
where the tildes and hats are the MLEs under the H_{0} and H_{1}, respectively. The critical threshold for declaring the existence of a QTL can be empirically determined from permutation tests [21].
Hypothesis tests for different genetic effects including the additive (α_{1}, β_{1}, α_{2}, β_{2}), dominant (γ_{1}, γ_{2}) and additive × additive (I_{αα}, I_{ αβ }, I_{ βα }, I_{ ββ }), additive × dominant (J_{ αγ }, J_{ βγ }), dominant × additive (K_{ γα }, K_{ γβ }) and dominant × dominant (L_{ γγ }) epistatic effects can be formulated, with the respective null hypotheses:
Under each null hypothesis, the genotypic values should be constrained by
for H_{0} : α_{1} = 0,
for H_{0} : β_{1} = 0,
for H_{0} : α_{2} = 0,
for H_{0} : β_{2} = 0,
for H_{0} : γ_{1} = 0,
for H_{0} : γ_{2} = 0,
for H_{0} : I_{ αα }= 0,
for H_{0} : I_{ αβ }= 0,
for H_{0} : I_{ βα }= 0,
for H_{0} : I_{ ββ }= 0,
for H_{0} : J_{ αγ }= 0,
for H_{0} : J_{ βγ }= 0,
for H_{0} : K_{ γα }= 0,
for H_{0} : K_{ γβ }= 0, and
for H_{0} : L_{ γγ }= 0, respectively. Each of these constraints is implemented with the EM algorithm as described above, which will lead to the MLEs of the genotypic values that satisfies equations (11)  (25), respectively. The critical thresholds for each of the tests (11)  (25) can be determined from simulation studies.
Results
A Worked Example
We use a real example of a forest tree to illustrate our multiallelic epistiatic QTL mapping method in an outbred population. The material was an interspecific F_{1} hybrid population between Populus deltoides (P_{1}) and P. euramericana (P_{2}). A total of 86 individuals were selected for QTL mapping. A genetic linkage map was constructed by using 74 SSR markers of segregating genotypes 12 × 34, which covers 822.35 cM of the whole genome and contains 14 linkage groups. The total number of roots per cutting (TNR) was measured and showed large variation in the hybrid population during the later development stage of adventitious rooting in water culture.
Through a systematic search over these linkage groups, the multiallelic espistatic model identifies six significant pairs of QTLs from different groups for TNR at the 5% significance level (Figure 1). The group × groupwide LR threshold for asserting that a pair of interacting QTLs exist was determined from 1000 permutation tests. Linkage group 2 has multiple regions that contain QTLs, which are located between markers L2_G_3592 and L2_O_10, markers L2_P_422 and L2_P_667, markers L2_P_667 and L2_G_876, and markers L2_O_286 and L2_O_222. These QTLs form five epistatic combinations by interacting with each other or with those on linkage groups 4, 7, 12 and 14 (Table 1). The sixth pair comes from linkage groups 6 and 12.
Table 1 gives the estimates of genetic effect parameters for the six pairs of interacting QTLs. At QTLs on linkage group 2, parent P. euramericana tends to contribute unfavorable alleles to root number, as seen by many negative β values, although this parent shows a better rooting capacity than parent P. deltoides. At these QTLs, parent P. deltoides generally contributes a smalleffect allele to root number, as seen by small α values. At the QTL on linkage group 6, this parent triggers a large positive additive effect. It is interesting to find that there are pronounced interactions between alleles from these two parents, as seen by large γ values, suggesting the importance of dominance in rooting capacity. In many cases, additive × additive epistatic effects are important, as indicated by many large I values. Our model can further discern which kind of additive × additive epistasis contribute. For example, the additive × additive epistasis between QTLs from linkage group 2 is due to the interaction between alleles from parent P. euramericana, while for QTL pair from linkage groups 2 and 14 this is due to the interaction between alleles from parent P. deltoides. The pattern of how the QTLs interact with each other in terms of additive × dominant, dominant × additive, and dominant × dominant epistasis can also be identified (Table 1).
Monte Carlo Simulation
We performed simulation studies to investigate the statistical properties of the multiallelic epistatic model. We simulated a fullsib family of sample size 400, 800 and 2000 derived from two outcrossing parents. Two QTLs were assumed at different locations of a 100 cMlong linkage group with 6 evenspaced markers. Phenotypic values of a quantitative trait for each individual were simulated as the genotypic values at these QTLs plus normally distributed errors (scaled to have different heritabilities, 0.1 and 0.4). Genotypic values are expressed in terms of genetic actions and interactions with true values tabulated in Table 2.
It was found that the QTL positions can well be estimated using our model (Table 2). The additive effects at individual QTLs and additive × additive epistatic effects can be reasonably estimated even when a modest sample size is used for a modest heritability. The other genetic effect parameters, especially dominant × dominant epistatic effects, need a large sample size to be reasonably estimated especially when the heritability is low. Because of a large number of parameters involved, the outcrossing design requires much larger sample sizes than backcross or F_{2} designs.
Discussion
The past two decades have seen a tremendous interest in developing statistical models for QTL mapping of complex traits inspired by Lander and Botestin's (1989) pioneered interval mapping [2, 3, 17, 22–25]. However, model development for QTL mapping in outbred populations, a group of species of great environmental and economical importance [26], has not received adequate attention. Only a few publications are available to QTL mapping in outcrossing species [12, 13]. In this article, we present a quantitative genetic model for studying the epistasis of multiallelic QTLs and a computational algorithm for estimating and testing epistatic interactions.
The central issue of QTL mapping for outcrossing populations is how to model genetic actions and interactions between multiple alleles at different QTLs. Traditional quantitative genetic models have been developed for biallelic genetic effects [16] and their extension to multiallelic cases have not been clearly explored. This study gives a first attempt to characterize epistatic interactions between multiallelic QTLs that pervade outcrossing populations. We partition additive effects at each QTL into two subcomponents based on different parental origins of alleles. Similarly, we partition the additive × additive epistasis into four different subcomponents, the additive × dominant epistasis into two subcomponents, and the dominant × additive epistasis into two subcomponents based on the interactions of alleles of different parental origins. These subcomponents have unique biological meanings because they are derived from distinct parents. In practice, hybridization is made between two genetically distant parents, thus an understanding of each of these subcomponent helps to study the genetic basis of heterosis.
We tested the new multiallelic epistasis model through simulation studies. In general, because of a number of parameters involved, a larger sample size is required to obtain reasonably precise estimation for QTL mapping in outcrossing populations. According to our experience, the increased heritability of traits by precise phenotyping can improve parameter estimation and model power than augmented experiment scales. We recommend that more efforts are given to field management that can improve the quality of phenotype measurements than experimental size. By analyzing a real data set from a poplar genetic study, the new model has been well validated. It is interesting to find that interactions between alleles from different poplar species contribute substantially to rooting capacity from cuttings, larger than genetic effects of alleles that operate alone. This result may help to understand the role of dominance in mediating heterosis.
Conclusions
We have developed a statistical model for mapping interactive QTLs in a fullsib family of outcrossing species. By capitalizing on traditional quantitative genetic theory, we define epistatic components due to interactions between two outcrossing multiallelic QTLs. An algorithmic procedure was derived to estimate all types of outcrossing epistasis and test their significance in controlling a quantitative trait. Our model provides a useful tool for studying the genetic architecture of complex traits for outcrossing species, such as forest trees, and fill a gap that occurs in genetic mapping of this group of important but underrepresented species.
References
 1.
Lander ES, Botstein D: Mapping Mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics. 1989, 121: 185199.
 2.
Zeng ZB: Precision mapping of quantitative trait loci. Genetics. 1994, 136: 14571468.
 3.
Lynch M, Walsh B: Genetics and Analysis of Quantitative Traits SinauerAssociates, Sunderland, MA; 1998.
 4.
Wu RL, Zeng ZB, McKend SE, O'Malley DM: The case for molecular mapping in forest tree breeding. Plant Breed Rev. 2000, 19: 4168.
 5.
Ritter E, Gebhardt C, Salamini F: Estimation of recombination frequencies and construction of RFLP linkage maps in plants from crosses between heterozy gous parents. Genetics. 1999, 125: 645654.
 6.
Ritter E, Salamini F: The calculation of recombination frequencies in crosses of allogamous plant species with applications to linkage mapping. Genet Res. 1996, 67: 5565. 10.1017/S0016672300033474.
 7.
Grattapaglia D, Sederoff RR: Genetic linkage maps of Eucalyptus grandis and Eucalyptus urophylla using a pseudotestcross: mapping strategy and RAPD markers. Genetics. 1994, 137: 11211137.
 8.
Maliepaard C, Jansen J, van Ooijen JW: Linkage analysis in a fullsib family of an outbreeding plant species: overview and consequences for applications. Genet Res. 1997, 70: 237250. 10.1017/S0016672397003005.
 9.
Wu RL, Ma CX, Painter I, Zeng ZB: Simultaneous maximum likelihood estimation of linkage and linkage phases in outcrossing species. Theor Pop Biol. 2002, 61: 349363. 10.1006/tpbi.2002.1577.
 10.
Lu Q, Cui YH, Wu RL: A multilocus likelihood approach to joint modeling of linkage, parental diplotype and gene order in a fullsib family. BMC Genet. 2004, 5: 20.
 11.
Stam P: Construction of integrated genetic linkage maps by means of a new computer package: JoinMap. Plant J. 1993, 3: 739744. 10.1111/j.1365313X.1993.00739.x.
 12.
Lin M, Lou XY, Chang M, Wu RL: A general statistical framework for mapping quantitative trait loci in nonmodel systems: Issue for characterizing linkage phases. Genetics. 2002, 165: 901913.
 13.
Wu S, Yang J, Huang YJ, Li Y, Yin T, Wullschleger SD, Tuskan GA, Wu RL: An improved approach for mapping quantitative trait loci in a pseudotestcross design: Revisiting a poplar genome study. Bioinformat Biol Insights. 2010, 4: 18.
 14.
Wullschleger SD, Yin TM, DiFazio SP, Tschaplinski TJ, Gunter LE, Davis MF, Tuskan GA: Phenotypic variation in growth and biomass distribution for two advancedgeneration pedigrees of hybrid poplar (Populus spp.). Can J For Res. 2005, 5: 17791789.
 15.
Whitlock MC, Phillips PC, Moore FBG, Tonsor SJ: Multiple fitness peaks and epistasis. Ann Rev Ecol Syst. 1995, 26: 601629. 10.1146/annurev.es.26.110195.003125.
 16.
Mather K, Jinks JL: Biometrical Genetics. Chapman & Hall London;, 3 1982.
 17.
Kao CH, Zeng ZB: Modeling epistasis of quantitative trait loci using Cockerham's model. Genetics. 2002, 160: 12431261.
 18.
Zhang B, Tong CF, Yin TM, Zhang XY, Zhuge Q, Huang MR, Wang MX, Wu RL: Detection of quantitative trait loci influencing growth trajectories of adventitious roots in Populus using functional mapping. Tree Genet Genom. 2009, 5: 539552. 10.1007/s112950090207z.
 19.
Mather K, Jinks JL: Biometrical Genetics. Chapman & Hall London;, 3 1982.
 20.
Wu RL, Ma CX, Casella G: Statistical Genetics of Quantitative Traits: LinkageMaps and QTL SpringerVerlag, New York; 2007.
 21.
Churchill GA, Doerge RW: Empirical threshold values for quantitative trait mapping. Genetics. 1994, 138: 963971.
 22.
Yi NJ, Xu SZ, Allison DB: Bayesian model choice and search strategies for mapping interacting quantitative trait loci. Genetics. 2003, 165: 867883.
 23.
Broman KW: Mapping quantitative trait loci in the case of a spike in the phenotype distribution. Genetics. 2003, 163: 11691175.
 24.
Zou F, Nie L, Wright FA, Sen PK: A robust QTL mapping procedure. J Stat Plan Infer. 2009, 139: 978989. 10.1016/j.jspi.2008.06.009.
 25.
Cheng JY, Tzeng SJ: Parametric and semiparametric methods for mapping quantitative trait loci. Computat Stat Data Analy. 2009, 53: 18431849. 10.1016/j.csda.2008.08.026.
 26.
Bradshaw HD, Stettler RF: Molecular genetics of growth and development in Populus. IV. Mapping QTLs with large effects on growth, form, and phenology traits in a forest tree. Genetics. 1995, 139: 963973.
Acknowledgements
This work is partially supported by NSF/IOS0923975, Changjiang Scholars Award, and "Thousandperson Plan" Award.
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CT derived the model and performed computer simulation and data analysis. BZ and MX collected the data from poplar hybrids. ZW and JS participated in simulation studies. XP participated in model design and result interpretation. MH conceived of the experiment. RW developed the model and algorithm, coordinated simulation and data analysis, and wrote the paper. All authors have read and approved the final manuscript.
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Tong, C., Zhang, B., Wang, Z. et al. Multiallelic epistatic model for an outbred cross and mapping algorithm of interactive quantitative trait loci. BMC Plant Biol 11, 148 (2011) doi:10.1186/1471222911148
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Keywords
 Quantitative Trait Locus
 Linkage Group
 Quantitative Trait Locus Mapping
 Epistatic Effect
 Quantitative Trait Locus Position