 Research article
 Open Access
Fast and accurate haplotype frequency estimation for large haplotype vectors from pooled DNA data
 Alexandros Iliadis^{1},
 Dimitris Anastassiou^{1} and
 Xiaodong Wang^{1}Email author
https://doi.org/10.1186/147121561394
© Iliadis et al.; licensee BioMed Central Ltd. 2012
Received: 30 May 2012
Accepted: 9 October 2012
Published: 30 October 2012
Abstract
Background
Typically, the first phase of a genome wide association study (GWAS) includes genotyping across hundreds of individuals and validation of the most significant SNPs. Allelotyping of pooled genomic DNA is a common approach to reduce the overall cost of the study. Knowledge of haplotype structure can provide additional information to single locus analyses. Several methods have been proposed for estimating haplotype frequencies in a population from pooled DNA data.
Results
We introduce a technique for haplotype frequency estimation in a population from pooled DNA samples focusing on datasets containing a small number of individuals per pool (2 or 3 individuals) and a large number of markers. We compare our method with the publicly available stateoftheart algorithms HIPPO and HAPLOPOOL on datasets of varying number of pools and marker sizes. We demonstrate that our algorithm provides improvements in terms of accuracy and computational time over competing methods for large number of markers while demonstrating comparable performance for smaller marker sizes. Our method is implemented in the "TreeBased Deterministic Sampling Pool" (TDSPool) package which is available for download at http://www.ee.columbia.edu/~anastas/tdspool.
Conclusions
Using a treebased determinstic sampling technique we present an algorithm for haplotype frequency estimation from pooled data. Our method demonstrates superior performance in datasets with large number of markers and could be the method of choice for haplotype frequency estimation in such datasets.
Keywords
Background
In recent years large genetic association studies involving hundreds or thousands of individuals have become increasingly available, providing opportunities for biological and medical discoveries. In these studies, hundreds of thousands of SNPs are genotyped for the cases and the controls, and discrepancies between the haplotype distributions indicate an association between a genetic region and the disease. Typically, the first phase of a GWAS includes genotyping across hundreds of individuals and validation of the most significant SNPs. One possible approach to reducing the overall cost of GWAS is to replace individual genotyping in phase I with allelotyping of pooled genomic DNA [1–6]. Here, equimolar amounts of DNA are mixed into one sample prior to the amplification and sequencing steps. After genotyping, the frequency of an allele in each position is given [5].
Rather than examining SNPs independent of each other, simultaneously considering the values of multiple SNPs within haplotypes (combinations of alleles at multiple loci in individual chromosomes) can improve the power of detecting associations with disease and is also of general interest with the pooled data. To facilitate haplotypebased association analysis it is necessary to estimate haplotype frequencies from pooled DNA data.
A variety of algorithms have been suggested to estimate haplotype frequencies from pooled data. Available methods fall into two large categories. The first category consists of methods that focus on accurate solutions for small pool sizes (2 or 3 individuals per pool) and considerably large genotype segments. Many well known approaches that focus on small pool sizes use an expectationmaximization (EM) algorithm for maximizing the multinomial likelihood [7–9]. Pirinen et al. [10] extended the gold standard PHASE algorithm [11] to the case of pooled data. They introduced a novel step in the Markov Chain Monte Carlo (MCMC) scheme, during which the haplotypes within each pool were shuffled to simulate individuals on which the original PHASE algorithm could be run to estimate the haplotypes. A method based on perfect phylogeny, HAPLOPOOL, was suggested in [12] and was supplemented with the EM algorithm and linear regression in order to combine haplotype segments. HAPLOPOOL has demonstrated superior performance in terms of accuracy and computational time with respect to the competing EM algorithms. The second category consists of methods that focus on large pools (order of hundred of individuals per pool) and considerably smaller genotype segments. For this scenario, Zhang et al. [13] first proposed a method (PoooL) for estimating haplotype frequencies using a normal approximation for the distribution of pooled allele counts. Imposing a set of linear constraints they transformed the EM algorithm to a constrained maximum entropy problem which they solved using the iterative scaling method. Kuk et al. [14] improved the PoooL methodology, using the ratio of normal densities approximation in the EM, which resulted to the AEM method. Gasbarra et al. [15] introduced a Bayesian haplotype frequency estimation method combining the pooled allele frequency data with prior database knowledge about the set of existing haplotypes in the population. Finally, HIPPO [16] used a multinormal approximation of the likelihood and a reversiblejump Markov chain Monte Carlo (RJMCMC) algorithm to estimate the existing haplotypes in the population and their frequencies. The HIPPO framework is also able to accommodate prior database knowledge for the existing haplotypes in the population and has demonstrated improvements in the performance over the approximate EM  algorithm [16]. In this study we will therefore compare our proposed algorithm with the top performing methods from each category as discussed above, namely HIPPO and HAPLOPOOL.
Naturally, pooling techniques are more prone to errors and offer less possibilities for assessing the quality of the data than individual genotyping. As argued and discussed by Kirkpatrick et al. [12], pooling errors have much greater effect on larger pool sizes as opposed to small pool sizes with respect to the number of incorrect allele calls and the subsequent haplotype estimation. In specific, if σ is the error standard deviation (SD) in the estimates of allele frequencies, 2* σ should be less than the difference between allowable frequency estimates, in order for clustering algorithms to be able to correct the error. As more individuals are included in each pool, the difference between allowable allele frequencies decreases, which results in a higher percentage of incorrect calls. For example in pools of two individuals where the difference between allowable frequency calls is 0.25 (0,0.25, 0.5 ,0.75,1), an accuracy of σ <0.125 will ensure a low rate of incorrect calls (<1%).
In a recent study Kuk et al. [17] examined the efficiency of pooling relative to no pooling using asymptotic statistical theory. They found that under linkage equilibrium (not a typical case!) pooling suffers loss in efficiency when there are more than three independent loci (2^{3} haplotypes) and up to four individuals per pool, whereas accuracy decreases with increasing pool size and number of loci. Rare alleles or linkage disequilibrium (LD) (or both) decrease the number of haplotypes that appear with nonnegligible frequencies and thus pooling could remain efficient for larger haplotype blocks. In general, pooling could still remain more efficient in the case where only a small number of haplotypes can occur with appreciable frequency, as also suggested in Barratt et al. [18], and while pool size is kept considerably small.
In this paper we propose a new treebased deterministic sampling method (TDSPool) for haplotype frequency estimation from pooled DNA data. Our method specifically focuses on small pool sizes and can handle arbitrarily large block sizes. In our study, we examine real data focusing on dense SNP areas, in which only a small number of haplotypes appear with appreciable frequency, so that our scenarios are within the limits of Kuk et al. [17]. We demonstrate that using our methodology we can achieve improved performance over existing stateoftheart methods in datasets with large number of markers.
Results
In order to compare the accuracy of frequency estimation between the different methods and under the different scenarios examined, we compared the predicted haplotype frequencies from a given method, f, to the goldstandard frequencies, g, observed in the actual population. The measure we used was the χ^{2} distance between the two distributions which is simply the result of the χ^{2} statistic, where g is the expected distribution, i.e., χ^{2}(f, g) = Σ_{i=1}^{ d }(f_{ i } − g_{ i })^{2}/g_{ i } and d is the number of gold standard haplotypes [12].
Datasets
To examine the performance of our methodology we have considered in our experiments real datasets for which estimates of the haplotype frequencies were already available and which cover a variety of dataset sizes.
Haplotypes and their estimated frequencies for the 3 loci dataset
Haplotype  Frequency 

1 0 0  0.082 
0 0 1  0.525 
1 0 1  0.283 
1 1 1  0.106 
Haplotypes and their estimated frequencies for the 10 loci dataset
Haplotype  Frequency 

1 1 1 1 0 1 1 0 0 0  0.033 
1 1 0 1 0 1 1 1 1 0  0.016 
1 1 0 1 0 0 1 0 0 1  0.017 
1 0 0 1 0 1 1 0 0 1  0.017 
1 1 0 1 0 1 1 0 0 1  0.017 
1 1 1 1 0 1 1 1 0 1  0.507 
0 1 0 1 1 0 0 1 1 1  0.017 
1 1 0 0 0 0 1 1 1 1  0.033 
0 1 0 1 0 0 1 1 1 1  0.1 
1 1 0 1 0 1 1 1 1 1  0.193 
1 1 1 1 1 1 1 1 1 1  0.05 
The third dataset consisted of SNPs from the first 7Mb (742 kb to 7124.8 kb) of the HapMap CEU population (HapMap 3 release 2 Phasing data). This chromosomal region was partitioned based on physical distance into disjoint blocks of 15 kb. The resulting blocks had a varying number of markers ranging from 2–28. For our purposes we have considered only the datasets that had more than 10 SNPs and less than 20 (which was the maximum number of loci so that HAPLOPOOL could produce estimates within a reasonable amount of time) which resulted in selecting a total of 80 blocks. On each block the parental haplotypes and their estimated frequencies were used as the true haplotype distribution. As in the previous cases, in each block two different pool sizes, 2 and 3 individuals per pool, were considered and four different number of pools per dataset.
Frequency estimation
For the 3 and 10 loci datasets the result presented is the average χ^{2} distance from a 100 simulation experiments, whereas in the HapMap dataset the result presented is the average χ^{2} distance on the 80 datasets considered. For the 3 loci dataset it can be seen that TDSPool and HAPLOPOOL produced similar accuracy. For the remaining two datasets with larger number of loci TDSPool demonstrated superior performance. For the HapMap dataset only TDSPool and HAPLOPOOL were evaluated since the maximum number of loci HIPPO can handle without prior knowledge of the major haplotypes in the population is 10. At the same time even though HAPLOPOOL can in principle handle larger datasets, due to excessive computational time for datasets with 24 and 28 loci we restricted our comparisons to datasets between 10 and 20 loci. We note here as well that since HIPPO is based on a central limit theorem it is likely to be a better approximation in large pools as opposed to small ones that we focus in our study.
From our experiments we can also see that the number of pools also affected accuracy. All algorithms demonstrated improved performance with increasing number of pools in the dataset.
Noise and missing data
In the previous subsection we have evaluated the performance of our method by simulating DNA pools without missing data and measurement errors. However, in allelotyping pooled DNA, allele frequencies may not be estimated properly in some practical situations and the data are consequently missing or have measurement errors.
For small number of loci, HAPLOPOOL achieves the best performance. However, for larger datasets TDSPool outperforms all competing methods.
Timing results
Timing results
Number of pools  

50  75  100  150  
3loci Dataset  
TDSPool  0.4458  0.4331  0.4743  0.4861  
0.4260  0.4772  0.5346  0.5350  
HaploPool  0.0697  0.0642  0.0607  0.0674  
0.0593  0.0681  0.0607  0.0691  
HIPPO  2.3593  3.0793  3.8856  5.3911  
2.4182  3.2047  4.1161  5.5873  
10loci Dataset  
TDSPool  0.8094  0.7778  1.0367  1.1259  
1.0269  1.0805  1.1804  1.3920  
HaploPool  0.5136  0.7381  0.9554  1.4012  
0.8531  1.2331  1.6247  2.4078  
HIPPO  59.5605  62.7163  64.1563  71.0505  
58.8816  64.6515  64.5386  73.9019  
HapMap  
Dataset  TDSPool  1.0189  1.1660  1.1765  1.5455 
1.8760  2.0830  2.1848  3.2719  
HaploPool  0.6737  0.9577  1.2679  1.8489  
1.1636  1.6928  2.2006  3.2905 
Discussion
We have introduced a new algorithm for estimating haplotype frequencies from datasets with pooled DNA samples and we have compared it with existing available packages. We have shown that for datasets with small number of loci our algorithm has comparable performance to stateoftheart methods in terms of accuracy and computational time but it demonstrates superior performance for datasets with larger number of loci.
Our method specifically focuses on small pool sizes and we have demonstrated the performance on pools of two or three individuals. In our experiments we have partitioned pooled genotype vectors in blocks of 4 SNPs as described in the "PartitionLigation" subsection. We have chosen to partition the pooled genotypes every 4 SNPs so that computations are performed fast and we avoid cases with huge number of solutions. Partitioning the dataset every 3 SNPs had negligible impact on the accuracy of our results (results not shown) whereas partitioning every 5 SNPs in general can produce block pool genotypes with thousands of solutions, especially when missing data occur.
In the framework developed by Pirinen [16], which had resulted in HIPPO, the algorithm was able to accommodate prior database information on existing haplotypes in a population. Similarly, our methodology offers a framework that can easily incorporate prior knowledge in the form of known haplotypes from the same population as that from which the target pools were created. When such existing haplotypes are known (such as those available from the HapMap), they can be easily introduced in the form of a prior for the counts in the TDSPool algorithm. The presence of the extra information will improve the frequency estimation accuracy in the target population.
Conclusions
We have introduced a new algorithm for estimating haplotype frequencies from pooled DNA samples using a TreeBased Deterministic sampling scheme. Algorithms for haplotype frequency estimation from pooled data fall into two categories. The first category consists of algorithms that focus on accurate solutions and allow for considerably large genotype segments and the second category of algorithms that focus on small segments but allow for a large number of individuals per pool. We have compared our methodology with stateoftheart algorithms from each category, namely HAPLOPOOL and HIPPO. We have focused on scenarios and datasets in which the use of pooling data is suggested for haplotype frequency estimation according to the study of Kuk et al. [17]. In specific, our method focuses on scenarios where pools contain 2 or 3 individuals and we have shown that for such scenarios our method demonstrates comparable or better performance compared with competing algorithms for a small number of loci and outperforms these algorithms for a large number of loci. Furthermore, our TDSPool methodology provides a straightforward framework for incorporating prior database knowledge into the haplotype frequency estimation.
Methods
In the beginning of the section we introduce some notation. We then present the prior and posterior distribution given the data and derive the state update equations for the TDSPool estimator. We further present the modified partitionligation procedure adjusted for the pooled data so that we are able to handle larger haplotype vectors and we finally give a summary of the proposed procedure.
Definitions and notation
Suppose we are given a set of pooled DNA measurements on L diallelic loci. We denote the two alleles at each locus by 0 and 1, for convenience of our representation. Following the common notation, we use the counts of allele 1 as the measurement for each allele on each pooled DNA sample, which can be converted from the estimated allele frequencies and consists the pool genotype. Therefore if the size of a pool is N individuals, the counts for each allele can vary between 0 and 2N.
Let us also define Z = {z_{1}, …z_{ M }} , where z_{ m } ∈ {0, 1}^{ L } is a binary string of length L in which 0 and 1 correspond to the two alleles at each locus, as the set containing all haplotype vectors of length L that are consistent with any pool genotype in the set A. To obtain Z from the given dataset A, we first enumerate for each α_{ i } the subset ψ_{ i } = {h_{ i }^{1}, …, h_{ i }^{ Y }} i = 1,…,T that contains all possible haplotype assignments which are consistent with α_{ i }. The set Z is then given simply by Z = ∪ _{i=1}^{ T }ψ_{ i } . A set of population haplotype frequencies θ = {θ_{1}, …, θ_{ M }} is also associated with the set Z of all possible haplotype vectors, where θ_{ m } is the probability with which the haplotype z_{ m } occurs in the total population.
Probabilistic model
Assuming random mating in the population it is clear that the number of each unique haplotype in H is drawn from a multinomial distribution based on the haplotype frequency θ[20]. This leads us to the use of the Dirichlet distribution as the prior distribution for θ[21] so that θ ∼ D(ρ_{1}, …, ρ_{ M })
With mean $E\left\{{\theta}_{i}\right\}=\frac{{\rho}_{i}}{{\displaystyle \sum _{j=1}^{M}{\rho}_{\text{j}}}}$
where we denote ρ_{ m }(t) m = 1,…,M as the parameters of the distribution of θ after the tth pool and I (z_{ m } − h_{ t,i }) with i = 1,…,2N_{ t } is the indicator function which equals 1 when z_{ m } − h_{t,i} is a vector of zeros, and 0 otherwise.
We have shown that the posterior distribution for θ is also Dirichlet with parameters as given in (1) and depends only on the sufficient statistics, T_{ t } = {ρ_{ m }(t), 1 ≤ m ≤ M} which can be easily updated based on T_{t−1}, h_{ t }, α_{ t } as given by (1) i.e. T_{ t } = T_{ t }(T_{t−1}, h_{ t }, α_{ t }).
Inference problem
Following the notation we used in our previous subsections we can summarize the frequency estimation problem as follows: Given A = {α_{1}, …, α_{ T }} the set of observed pool genotype vectors and Z = {z_{1}, …, z_{ M }} the set of haplotypes compatible to the pool genotypes in A we wish to infer H = {h_{1}, …, h_{ T }} the unknown haplotypes in each pool and θ = {θ_{1}, …, θ_{ M }} the haplotype frequencies of all the haplotypes occurring in the population.
Computational algorithm (TDSPool)
Similar to traditional Sequential Monte Carlo (SMC) methods, we assume that by the time we have processed pool genotype α_{ t1 } we have K sets of solution streams (i.e. sets of candidate haplotypes for pools 1,…, t1) and their associated weights $\left\{\left({H}_{t1}^{\left(k\right)}{w}_{t1}^{\left(k\right)}\right),k=1,\dots ,K\right\}$ properly weighted with respect to the posterior distribution p(H_{t−1}A_{t−1}).
where ${W}_{t1}={\displaystyle \sum _{k=1}^{K}{w}_{t1}^{\left(k\right)}\text{,}}$and I (●) is the indicator function such that I (xy)=1 for x = y and I (xy) = 0 otherwise.
When we process the pool genotype t we would like to make an online inference of the haplotypes H_{ t } based on the pool genotypes A_{ t }. Let us further assume that there are K^{ ext } possible haplotype solutions compatible with the genotype of the tth pool, i.e., h_{ t }^{ i }, i = 1, …, K^{ ext } .
Before we move to the derivation of the state update equation we note here that in the following we will use the fact that for the unknown parameters θ, as we have shown in "Probabilistic Model" subsection, under certain assumptions the prior and posterior distribution are Dirichlet and depend only on a set of sufficient statistics T_{ t } = T_{ t }(T_{t−1}, h_{ t }, α_{ t })
where ${\rho}_{{h}_{t,i}}\left(t1\right)=\left\{{\rho}_{{z}_{m}}\left(t1\right):{h}_{t,i}={z}_{m}\right\}$
Assuming that we have approximated p(H_{t−1}A_{t−1}) as in (2), we can approximate p(H_{ t }A_{ t }) using (3) as${\widehat{p}}^{\mathit{ext}}\left({H}_{t}{A}_{t}\right)=\frac{1}{{W}_{t}^{\mathit{ext}}}{\displaystyle \sum _{k=1}^{K}{\displaystyle \sum _{i=1}^{Kext}{w}_{t}^{\left(k,i\right)}I\left({H}_{t}\left[{H}_{t1}^{\left(k\right)},\left({h}_{t,1}^{i},\dots ,{h}_{t,2{N}_{t}}^{i}\right)\right]\right)}}$_{.}
PartitionLigation
In the partition phase the dataset is divided into small segments of consecutive loci. Once the blocks are phased, they are ligated together using a modified extension of the PartitionLigation (PL) method [21] for the case of pooled data.
In our current implementation to be able to derive all possible solution combinations for each pool genotype efficiently we have decided to keep the maximum block length to 4 SNPs. Clearly the more SNPs are included in a block the more information about the LD patterns we can capture but at the same time the number of possible combinations increases and becomes prohibitive for more than 5 SNPs. For our experiments in a dataset with L loci we have considered L/4 blocks of 4 consecutive loci and the remaining SNPs were treated as a separate block.
The result of phasing for each block is a set of haplotype solutions for each pool genotype. Two neighbouring blocks are ligated by creating merged solutions for each pool genotype from all combinations of the block solutions, one from each block. When creating a merged solution for a pool genotype from the two separate solutions (one from each block), since we do not know which haplotypes belong to the same chromosome, all different possible assignments are examined. The TDSPool algorithm is then repeated in the same manner as it was for the individual blocks.
Furthermore, the order in which the individual blocks are ligated is not predetermined. We first ligate the blocks that would produce in each step the minimum entropy ligation. This procedure allows us to ligate first the most homogeneous blocks so that we have more certainty in the solutions that we produce while moving in the ligation procedure.
Summary of the proposed algorithm
Routine 1

Set the current number of streams m = 1. Define K as the maximum number of streams allowed. Define H_{0}^{1} ={}.

For t = 1, 2,…

○ Find the K^{ ext } possible haplotype configurations compatible with the pool genotype of the tth pool.

○ For k = 1,2,…, m , j = 1,…,K^{ ext }

▪ Enumerate all possible particle extensions ${H}_{t}^{\left(k,j\right)}=\left[{H}_{t1}^{\left(k\right)},\left({h}_{t,1}^{j},\dots ,{h}_{t,2{N}_{t}}^{j}\right)\right]$

▪j compute the weights w_{ t }^{(k,j)} according to (4)


○ Select and preserve M = min (K, m· K^{ ext }) distinct sample streams {H_{ t }^{(k)}, k = 1,…,M} with the highest importance weights {w_{ t }^{(k)}, k = 1,…,M} from the set {H_{ t }^{(k,j)}, w_{ t }^{(k,j)}, k = 1,…,m, j = 1,…, K^{ ext } }

○ Update the number of counts of each encountered haplotype in each stream

○ Set m = M

TDSPool ALGORITHM

Partition the genotype dataset G into B subsets.

For b = 1,…,B , apply Routine 1 so that all segments are phased and for each one keep all the solutions contained in the top K particles.

Until all blocks are ligated, repeat the following

○ Find the blocks that if ligated would produce the minimum entropy

○ Ligate the blocks, following the procedure described in the PartitionLigation section

Declarations
Authors’ Affiliations
References
 Bansal A, van den Boom D, Kammerer S, Honisch C, Adam G, Cantor CR, Kleyn P, Braun A: Association testing by DNA pooling: an effective initial screen. Proc Natl Acad Sci U S A. 2002, 99 (26): 1687116874. 10.1073/pnas.262671399.PubMed CentralView ArticlePubMedGoogle Scholar
 Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G: Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet. 1997, 61 (3): 734747. 10.1086/515512.PubMed CentralView ArticlePubMedGoogle Scholar
 Norton N, Williams NM, O'Donovan MC, Owen MJ: DNA pooling as a tool for largescale association studies in complex traits. Ann Med. 2004, 36 (2): 146152. 10.1080/07853890310021724.View ArticlePubMedGoogle Scholar
 Pearson JV, Huentelman MJ, Halperin RF, Tembe WD, Melquist S, Homer N, Brun M, Szelinger S, Coon KD, Zismann VL: Identification of the genetic basis for complex disorders by use of poolingbased genomewide singlenucleotidepolymorphism association studies. Am J Hum Genet. 2007, 80 (1): 126139. 10.1086/510686.PubMed CentralView ArticlePubMedGoogle Scholar
 Sham P, Bader JS, Craig I, O'Donovan M, Owen M: DNA Pooling: a tool for largescale association studies. Nat Rev Genet. 2002, 3 (11): 862871.View ArticlePubMedGoogle Scholar
 Zuo Y, Zou G, Zhao H: Twostage designs in case–control association analysis. Genetics. 2006, 173 (3): 17471760. 10.1534/genetics.105.042648.PubMed CentralView ArticlePubMedGoogle Scholar
 Ito T, Chiku S, Inoue E, Tomita M, Morisaki T, Morisaki H, Kamatani N: Estimation of haplotype frequencies, linkagedisequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data. Am J Hum Genet. 2003, 72 (2): 384398. 10.1086/346116.PubMed CentralView ArticlePubMedGoogle Scholar
 Wang S, Kidd KK, Zhao H: On the use of DNA pooling to estimate haplotype frequencies. Genet Epidemiol. 2003, 24 (1): 7482. 10.1002/gepi.10195.View ArticlePubMedGoogle Scholar
 Yang Y, Zhang J, Hoh J, Matsuda F, Xu P, Lathrop M, Ott J: Efficiency of singlenucleotide polymorphism haplotype estimation from pooled DNA. Proc Natl Acad Sci U S A. 2003, 100 (12): 72257230. 10.1073/pnas.1237858100.PubMed CentralView ArticlePubMedGoogle Scholar
 Pirinen M, Kulathinal S, Gasbarra D, Sillanpaa MJ: Estimating population haplotype frequencies from pooled DNA samples using PHASE algorithm. Genet Res (Camb). 2008, 90 (6): 509524. 10.1017/S0016672308009877.View ArticleGoogle Scholar
 Stephens M, Scheet P: Accounting for decay of linkage disequilibrium in haplotype inference and missingdata imputation. Am J Hum Genet. 2005, 76 (3): 449462. 10.1086/428594.PubMed CentralView ArticlePubMedGoogle Scholar
 Kirkpatrick B, Armendariz CS, Karp RM, Halperin E: HAPLOPOOL: improving haplotype frequency estimation through DNA pools and phylogenetic modeling. Bioinformatics. 2007, 23 (22): 30483055. 10.1093/bioinformatics/btm435.View ArticlePubMedGoogle Scholar
 Zhang H, Yang HC, Yang Y: PoooL: an efficient method for estimating haplotype frequencies from large DNA pools. Bioinformatics. 2008, 24 (17): 19421948. 10.1093/bioinformatics/btn324.View ArticlePubMedGoogle Scholar
 Kuk AY, Zhang H, Yang Y: Computationally feasible estimation of haplotype frequencies from pooled DNA with and without HardyWeinberg equilibrium. Bioinformatics. 2009, 25 (3): 379386. 10.1093/bioinformatics/btn623.View ArticlePubMedGoogle Scholar
 Gasbarra D, Kulathinal S, Pirinen M, Sillanpaa MJ: Estimating haplotype frequencies by combining data from large DNA pools with database information. IEEE/ACM Trans Comput Biol Bioinform. 2011, 8 (1): 3644.View ArticlePubMedGoogle Scholar
 Pirinen M: Estimating population haplotype frequencies from pooled SNP data using incomplete database information. Bioinformatics. 2009, 25 (24): 32963302. 10.1093/bioinformatics/btp584.View ArticlePubMedGoogle Scholar
 Kuk AY, Xu J, Yang Y: A study of the efficiency of pooling in haplotype estimation. Bioinformatics. 2010, 26 (20): 25562563. 10.1093/bioinformatics/btq492.View ArticlePubMedGoogle Scholar
 Barratt BJ, Payne F, Rance HE, Nutland S, Todd JA, Clayton DG: Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design. Ann Hum Genet. 2002, 66 (Pt 5–6): 393405.View ArticlePubMedGoogle Scholar
 Jain S, Tang X, Narayanan CS, Agarwal Y, Peterson SM, Brown CD, Ott J, Kumar A: Angiotensinogen gene polymorphism at −217 affects basal promoter activity and is associated with hypertension in AfricanAmericans. J Biol Chem. 2002, 277 (39): 3688936896. 10.1074/jbc.M204732200.View ArticlePubMedGoogle Scholar
 Excoffier L, Slatkin M: Maximumlikelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol. 1995, 12 (5): 921927.PubMedGoogle Scholar
 Niu T, Qin ZS, Xu X, Liu JS: Bayesian haplotype inference for multiple linked singlenucleotide polymorphisms. Am J Hum Genet. 2002, 70 (1): 157169. 10.1086/338446.PubMed CentralView ArticlePubMedGoogle Scholar
Copyright
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.