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Association mapping through heuristic evolutionary history reconstructionapplication to GAW15 Problem 3
BMC Proceedings volume 1, Article number: S131 (2007)
Abstract
This paper presents a novel method of identifying phenotypically important regions of the genome. It involves a form of association mapping that works by summarizing properties of the ancestral recombination graph (ARG) of a sample of unrelated phenotyped and genotyped individuals. By breaking the sample into many small subsamples and averaging the results, it becomes computationally tractable to measure the degree to which the evolutionary history of any locus is consistent with the distribution of the phenotypes in the sample. Analysis of simulated rheumatoid arthritis data demonstrates the efficiency and effectiveness of this method in identifying loci of large phenotypic effect.
Background
Explicit reconstruction of the evolutionary history of a sample can provide a powerful tool for detecting genetic contributions to phenotypic variation in a population. This new method exploits the fact that an allele shared among individuals in a sample that contributes to similarities of those individuals' phenotypes must have originated in an ancestral lineage shared only by those individuals. Therefore, regions of the genome containing genes that contribute to the differences among individuals in the sample will tend to have evolutionary histories that reflect the phenotypic distributions of those individuals. Other regions not contributing to the phenotype in question, will, due to recombination, have histories that are uncorrelated with the distribution of phenotypes.
Cladistic analyses in association studies are a concept that date back to the late 1980s [1], and have been implemented several times since then [2–7]. Due to the complexities of withinpopulation evolutionary histories, they have tended to employ clustering algorithms which result in decidedly nonevolutionary cladograms of individuals.
This paper considers the case of phased haplotype data drawn from a population of binary phenotypes. Given infinite computing power, the process would involve using the genetic data to infer the entire ancestral recombination graph (ARG) of the sample. This would give the entire set of evolutionary relationships of every piece of every haplotype with every other piece of every haplotype. From there it would be a simple matter to pick the branches of the graph that most consistently divide the sample into groups of cases and controls, and then to infer which segments of the haplotypes those branches describe. This is not a feasible approach with current or developing technology, so it is necessary to describe a heuristic method for capturing the most important signal from this graph without reconstructing it in its entirety.
What makes ARGs so difficult to reconstruct is that the number of possible ARGs for a sample increases exponentially with the number of haplotypes in the sample. While it is not difficult to infer an optimal ARG for a sample of extremely small size, it quickly becomes intractable for sample sizes even in the tens of haplotypes. This method capitalizes on the relative ease of estimating ARGs for small sample sizes by successively computing ARGs for many small subsamples from within the set of haplotypes. For each site in each subsample, it is easy to determine whether that ARG correctly divides the subsample cases from the subsample controls. The frequency across subsamples is then the test statistic for determining the general trend in the topology of the overall ARG at each site. This statistic is a measure of the degree to which the history of a locus is consistent with the resulting phenotypic distribution of the haplotypes and will be referred to as the consistency of the sample.
Methods
Algorithm
This algorithm is an iterative process of selecting and analyzing subsets of the data. Each iteration starts with randomly selecting quartets of haplotypes composed of two control haplotypes and two unrelated case haplotypes. The program beagle [8] is used to infer the minimum number and location of recombinations necessary for each quartet to conform to an infinite sites model of evolution. Beagle scans the haplotypes for pairs of markers at which all four possible gametes are present. Without invoking recurrent mutation, this pattern indicates the presence of a recombination event somewhere between such marker pairs. Beagle assigns a minimum set of locations of recombination events that satisfies all such pairs. These are used to divide the haplotypes in the quartet into a set of genomic segments each consistent with a single tree for an evolutionary history.
Next, each of these segments is passed to the pars program in the package PHYLIP [9] to generate a single most parsimonious tree reflecting the history of that segment. This is the inferred evolutionary tree that minimizes the number of mutation events to describe all of the differences between the sequences. Of the three possible topologies for an unrooted tree with four taxa and no ambiguities (Fig. 1), only one will contain a branch that separates the two cases from the two controls. Segments generating a tree with this topology are considered "consistent". Either of the other two topologies is considered "inconsistent". Segments that do not unambiguously generate a maximum parsimony tree that is either consistent or inconsistent are thrown out.
After each segment is analyzed, the frequency across quartets in which each site finds itself in a consistent segment is calculated. This frequency, the consistency of the sample, is used as the test statistic. Elevated levels of consistency correspond to sites better able to explain the differences between case and control phenotypes. The amount of information learned from the data increases with each iteration but does so with asymptotically diminishing returns once every possible quartet has been picked.
Assessing significance
The significance of results is addressed through classical hypothesis testing. The data are modeled as being drawn at random from two populations, one of case haplotypes and one of control haplotypes. Every mutation in the history of the sample distinguishes between two alleles and creates two types of haplotypes, one with the ancestral allele at that site and one with the derived allele. If a particular mutation contributes to the probability of disease, then haplotypes containing that allele will be overrepresented in the case population. The null hypothesis is that the two types are represented with equal frequency in both the case and control populations.
A given data set can be summarized as having K_{1} case haplotypes with a_{1} copies of one type of haplotype and (K_{1}  a_{1}) of the other, and K_{2} control haplotypes with a_{2} and (K_{2}  a_{2}) copies of the two types of haplotypes respectively. As all the trees are unrooted, it is not necessary to identify which type is ancestral and which is derived. Therefore, which type is labeled (a) is an arbitrary designation.
The probability of a randomly drawn quartet being counted as consistent, p(a_{1}, a_{2}, K_{1}, K_{2}), can be calculated as
This is the probability of selecting a quartet composed of two haplotypes of one type from the control set and two haplotypes of the other type from the case set (which are the quartets that contribute to the signal in the data) plus 1/3 times the probability of selecting a quartet that contains three or four haplotypes of the same type and one or zero of the other (these quartets are uninformative and contribute only random noise).
The probability of a site being counted as consistent x times after N quartets have been analyzed should be calculated as
This is essentially a binomial sampling probability with p(a_{1}, a_{2}, K_{1}, K_{2}) being the chance of success on a particular trial, summed over all the possible values of the random variables a_{1} and a_{2} times their probability densities, g(a_{1}, K_{1}, α) and g(a_{2}, K_{2}, α), which are the binomial sampling probabilities of drawing a of the arbitrarily labeled haplotypes in K samples from a total population where the labeled type of haplotype is at frequency α.
Because the probability densities of a_{1} and a_{2} depend on the random variable α, the whole statement has to be integrated over all possible values of α times its probability density, f(α). Unfortunately, f(α) is unknown, so exact marginal probabilities cannot be calculated directly. However, for values of consistency above 1/3, which are the only ones of interest, the likelihood of the null hypothesis is at a maximum when α = 0.5, so assuming α = 0.5 and calculating pvalues by summing the probabilities of finding the observed or higher number of consistent quartets is conservative.
Results
Applied to the highdensity simulated SNPs of Replicate 1 of the Genome Analysis Workshop 15 Problem 3 data set, the algorithm correctly identifies Locus D as a site of great importance in determining simulated disease status. Figure 2 shows calculated consistency values along the chromosome after analyzing 1000 quartets. Using the entire data set of 3000 case haplotypes and 2000 control haplotypes gives an estimated pvalue of less than 10^{308} at the correct locus. This is the lowest pvalue for the chromosome, and in fact, the pvalue may be considerably lower than this because smaller values are difficult to compute accurately. The actual numerical value has little meaning beyond demonstrating the vanishingly small probability of getting such a signal by chance. Figures 2b and 2c represent the same analysis carried out on smaller random subsets of the data. In Figure 2b only a random subset of 10% of the haplotypes are used. The algorithm still correctly identifies the simulated locus and estimates a pvalue less than 10^{65}. In comparison, a simple chisquared test yields a pvalue of 10^{52} at the correct locus. Figure 2c uses a random subset of 1% of the haplotypes, still correctly identifies the proper locus, and gives a pvalue of less than 10^{11}. The chisquared test on these data gives a pvalue of 10^{5}.
Discussion
There are several practical matters to consider in applying this method. The first is that while the simulated data analyzed in this paper were given as fully phased haplotypes, most real data are only known as unphased genotypes. Therefore, an additional step of estimating phase is necessary. There are several widely used algorithms for accomplishing this, such as fastPHASE [10] or HAPLOTYPER [11]. These algorithms use the population genotype frequencies in the samples to estimate the haplotype frequencies contributing to the sample. They are generally very accurate over short ranges but can introduce errors, essentially artificial recombination events between haplotypes, between markers with very little linkage disequilibrium. These types of errors do not influence consistency estimates much at all, because all of the information used in estimating consistency comes from closely linked markers. Furthermore, introducing artificial recombinations into the data set can only increase the type II error rate, not the type I error rate.
Similarly, this method is conservative to errors introduced by violations of the infinite sites model of evolution. Beagle invokes the infinite sites model to infer the existence of a recombination event. Recurrent mutation could cause beagle to include extra recombination points. The only detriment to this is that pars must now estimate two trees from the information that it would otherwise use to estimate just a single tree. This would cause a very local reduction in power but cannot create false positives. A massive departure from the infinite sites model could mean that the trees produced by pars are poor reconstructions of the true historical events. However, this too should only reduce the sensitivity of the test, not inflate the type I error rate.
The consistency estimate is unbiased for all values of N. As N increases, the pvalue of any consistency estimate above 1/3 decreases. There are diminishing returns as N becomes a sizeable fraction of all the possible quartets. As the number of possible quartets is generally far larger than is reasonable (or worthwhile) to examine, a practical guideline would be to continue running the algorithm until effects of a minimally interesting consistency value are significant.
Conclusion
Population genetic data arise through a well understood and well modeled process of evolution. In association mapping studies, treating each locus and each haplotype as independent, unrelated trials, as in the chisquared test and other simple regression analyses, robs an investigator of much useful information in her or his data and opens the door to spurious results. Making use of our understanding of the process through which these data are created allows us to fashion more powerful and more reliable methods. The method of consistency shows that even a simple algorithm using piecewise approximations of evolutionary histories can offer a great increase in statistical power. Additionally, statistics built on biological models can represent easily intuited biological properties. Unlike a chisquared statistic, consistency is itself a measurement that relates directly to the biological phenomenon that it tests.
Abbreviations
 ARG:

ancestral recombination graph
References
 1.
Templeton A, Boerwinkle E, Sing C: A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila. Genetics. 1987, 117: 343351.
 2.
Templeton A: A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping or DNA sequencing. V. Analysis of case/control sampling designs: Alzheimer's disease and the apoprotein E locus. Genetics. 1995, 140: 403409.
 3.
Molitor J, Marjoram P, Thomas D: Finescale mapping of diseases with multiple mutations via spatial clustering techniques. Am J Hum Genet. 2003, 73: 13681384. 10.1086/380415.
 4.
Durrant C, Zondervan K, Cardon L, Hunt S, Deloukas P, Morris A: Linkage disequilibrium mapping via cladistic analysis of singlenucleotide polymorphism haplotypes. Am J Hum Genet. 2004, 75: 3543. 10.1086/422174.
 5.
Sillanpaa M, Bhattacharjee M: Bayesian associationbased fine mapping in small chromosomal segments. Genetics. 2005, 169: 427439. 10.1534/genetics.104.032680.
 6.
Templeton A, Maxwell T, Posada D, Stengård J, Boerwinkle E, Sing C: Tree scanning: a method for using haplotype trees in phenotype/genotype association studies. Genetics. 2005, 169: 441453. 10.1534/genetics.104.030080.
 7.
Tzeng J: Evolutionarybased grouping of haplotypes in association analysis. Genet Epidemiol. 2005, 28: 220231. 10.1002/gepi.20063.
 8.
Lyngsø R, Song Y, Hein J: Minimum recombination histories by branch and bound, proceedings of workshop on algorithms in bioinformatics. Lect Notes Comput Sci. 2005, 3692: 239250.
 9.
Felsenstein J: PHYLIP (Phylogeny Inference Package) Version 3.6. 2005, Seattle: Department of Genome Sciences, University of Washington
 10.
Scheet P, Stephens M: A fast and flexible statistical model for largescale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet. 2006, 78: 629644. 10.1086/502802.
 11.
Niu T, Qin Z, Xu X, Liu J: Bayesian haplotype inference for multiple linked single nucleotide polymorphisms. Am J Hum Genet. 2002, 70: 157169. 10.1086/338446.
Acknowledgements
AP appreciates discussions with Paul Marjoram, Magnus Nordborg, Simon Tavaré, and John Molitor.
This article has been published as part of BMC Proceedings Volume 1 Supplement 1, 2007: Genetic Analysis Workshop 15: Gene Expression Analysis and Approaches to Detecting Multiple Functional Loci. The full contents of the supplement are available online at http://0www.biomedcentral.com.brum.beds.ac.uk/17536561/1?issue=S1.
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Platt, A. Association mapping through heuristic evolutionary history reconstructionapplication to GAW15 Problem 3. BMC Proc 1, S131 (2007). https://0doiorg.brum.beds.ac.uk/10.1186/175365611S1S131
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DOI: https://0doiorg.brum.beds.ac.uk/10.1186/175365611S1S131
Keywords
 Association Mapping
 Phase Haplotype
 Ancestral Recombination Graph
 Unrelated Trial
 Infinite Site Model