Volume 6 Supplement 7
Proceedings of the Great Lakes Bioinformatics Conference 2012
A ν-support vector regression based approach for predicting imputation quality
- Yi-Hung Huang^{1, 2}Email author,
- John P Rice^{3},
- Scott F Saccone^{3},
- José Luis Ambite^{4},
- Yigal Arens^{4},
- Jay A Tischfield^{5} and
- Chun-Nan Hsu^{1, 4}Email author
DOI: 10.1186/1753-6561-6-S7-S3
© Huang et al.; licensee BioMed Central Ltd. 2012
Published: 13 November 2012
Abstract
Background
Decades of genome-wide association studies (GWAS) have accumulated large volumes of genomic data that can potentially be reused to increase statistical power of new studies, but different genotyping platforms with different marker sets have been used as biotechnology has evolved, preventing pooling and comparability of old and new data. For example, to pool together data collected by 550K chips with newer data collected by 900K chips, we will need to impute missing loci. Many imputation algorithms have been developed, but the posteriori probabilities estimated by those algorithms are not a reliable measure the quality of the imputation. Recently, many studies have used an imputation quality score (IQS) to measure the quality of imputation. The IQS requires to know true alleles to estimate. Only when the population and the imputation loci are identical can we reuse the estimated IQS when the true alleles are unknown.
Methods
Here, we present a regression model to estimate IQS that learns from imputation of loci with known alleles. We designed a small set of features, such as minor allele frequencies, distance to the nearest known cross-over hotspot, etc., for the prediction of IQS. We evaluated our regression models by estimating IQS of imputations by BEAGLE for a set of GWAS data from the NCBI GEO database collected from samples from different ethnic populations.
Results
We construct a ν-SVR based approach as our regression model. Our evaluation shows that this regression model can accomplish mean square errors of less than 0.02 and a correlation coefficient close to 0.75 in different imputation scenarios. We also show how the regression results can help remove false positives in association studies.
Conclusion
Reliable estimation of IQS will facilitate integration and reuse of existing genomic data for meta-analysis and secondary analysis. Experiments show that it is possible to use a small number of features to regress the IQS by learning from different training examples of imputation and IQS pairs.
Background
In the past decade, the data sets collected for genome wide association studies (GWAS) have grown geometrically. Reusing these valuable data in new studies is difficult because they are collected through different study designs and on different platforms. Various imputation algorithms (e.g., IMPUTE [1], BEAGLE [2–7], and MACH [8]) have been developed to predict the individual genotypes at un-typed markers. Although these imputation algorithms have already been put to use, the methods of measuring imputation quality are still rarely addressed. The imputation quality score of the single-nucleotide polymorphism (SNP) genotypes are quite different at distinct loci. For this reason, we want to investigate how to measure the imputation quality for a particular SNP that is imputed by these algorithms. After the imputation quality measurement is established, researchers can pay more attention to those poorly-imputed SNPs in the data integration process. Recently, [9] proposed a new statistic for assessing the imputation reliability and it is designated as the imputation quality score (IQS). The IQS has been shown to be commensurate with the true quality of the imputation and successfully applied to filter false positive associations in GWAS studies that use imputed genotypes [9].
Marginal cross classification of the genotypes used for the computation of IQS
True genotypes | ||||
---|---|---|---|---|
Imputed Genotypes | AA | AB | BB | Total |
AA | n _{11} | n _{12} | n_{13} | n _{1.} |
AB | n _{21} | n _{22} | n _{23} | n _{2.} |
BB | n _{31} | n _{32} | n _{33} | n _{3.} |
Total | n _{.1} | n _{.2} | n._{3} | n.. |
Assessment of P_{ o }, P_{ c }, and IQS needs the true genotypes to be known. [9] showed that for the same population and the same locus imputed using the same set of loci with known genotypes, the estimated IQS are highly correlated. We showed it by dividing a sample by half and imputing SNPs of the Illumina 1 M array using the SNP genotyping results from the Illumina 550 K array, and then we estimated the IQS scores. We obtained a correlation coefficient of 0.99 for the IQS scores for the same set of imputed SNPs. That is, we can expect that IQS scores will be nearly the same if the population, the imputed SNPs, and the SNPs of known genotypes, are identical. If there are previously estimated IQS scores available that match these conditions, then the scores can be reused. Therefore, it is possible to obtain IQS scores without knowing true genotypes by querying the IQS from a pre-constructed IQS database.
However, exhausting all populations and combinations of imputation loci to establish such a database of all useful IQS may take considerable resources. Here, we try to develop a computational method to estimate IQS without known true genotypes. We assess whether or not it is possible to build a regression model from imputations of SNP sites with known alleles, and then use the regression model to estimate IQS for SNPs with unknown alleles. The idea is to use additional statistical information to build a regression model to predict the IQS. Also, in practice, people work with specific sets of variants and this method will facilitate creation of a database of the IQS of those variants.
Methods and materials
ν -Support vector regression
In a multi-dimensional regression problem, we have a data set of l d-dimensional independent variables x_{ i } ∈ ℝ^{ d }, i = 1,..., l and dependent variables y_{ i } ∈ ℝ. In our IQS regression problem, y_{ i } represents the true IQS and x_{ i } denotes the input feature vector. The goal is to find a function that approximates y_{ i }. A solution of this problem based on a kernel method is to find the function y_{ i } ≈ f(x_{ i }, w, b) = w. φ (x_{ i }) - b, where w and b ∈ ℝ^{ d } are parameters and φ : ℝ^{ d } → ℝ^{ d } is a mapping such that there exists a kernel function that computes the inner product φ (x_{ i }). φ (x_{ j }) = k(x_{ i }, x_{ j }). Because the radial basis function (RBF) can preserve a relatively high accuracy in comparison with other kernel functions (data not shown), our choice of the kernel function is the RBF kernel [11, 12].
The parameter C is used to determine the complexity of model and controls the tradeoff between the training error minimization and the model complexity. If it is too small, the model may underfit the data. The parameter ε serves as the tolerance of errors of the regression. Combined with the slack variables ξ_{ i } ${\xi}_{i}^{*}$ we have a soft-margin approach to regression that can be flexibly adjusted [11, 12].
Moreover, the parameter ν can serve as an upper bound for the fraction of margin errors, and a lower bound for the fraction of the number of support vectors. In comparison with C, to select a suitable ν would be more intuitive [13, 14]. Therefore, we chose ν-SVR over ε-SVR for our IQS prediction model. This model is also known to provide high out-of-sample generalization performance.
We chose LibSVM [16] as our implementation of the ν-SVR model. The parameter γ in the radial basis function is set as 1/d. The parameter ν was searched within {0.1, 0.2, 0.3, . . . 1.0} and an optimal value of ν were selected by applying a 10-fold cross validation on the training data set. The regression model can be applied to approximate P_{ o } and P_{ c } as well as the IQS.
Features generation
- 1.
Chromosome position: The chromosome where the SNP located.
- 2.
Physical position: The position of the imputed SNP in bp.
- 3.
Minor allele frequency (MAF): Previously, [9] have shown that the minor allele frequency is an important variable correlated with the true IQS. The above three features are available in the annotation file from the genotyping platform provider.
- 4.
B allele frequency: This is derived from the allele signal intensity measurement for each locus of each individual in the raw CEL files. The raw CEL files are available from the Hapmap samples [17]. For each imputed SNP, we used the mean of the B allele frequency of the SNP on the samples of the corresponding ethnic population.
- 5.
MAF in the reference panel: In addition to using the available MAF provided by the annotation file, we also consider the MAF in the reference panel.
- 6.
Ratio of genotypes AA/AB: It is used to to indicate the proportion of genotype AA for each imputed SNP in the reference panel.
- 7.
Ratio of genotypes BB/AB: Similar to feature 6, it is used to to indicate the proportion of genotype BB for each imputed SNP in the reference panel.
- 8.
Distance to the nearest genotyped SNP: This is to capture an indication that the imputation quality will be better if the nearest genotyped SNP in the inference panel is closer.
- 9.
Distance to the nearest recombination hotspot: The distance to the nearest recombination hotspot also plays an important role in the quality of the imputation. We used the recombination rates and hotspots available in the release version phase II build b35 to GRCh37 from the International HapMap Project [17].
- 10.
The nearest recombination hotspot's recombination rate (cM/Mb, centiMorgans per megabase): This variable is important in the imputation process. The IMPUTE2 program uses it explicitly as a required input for the imputation [1, 18].
- 11.
Posterior probability estimated by the imputation program: This variable is available from the output of the imputation program. The Beagle program provides the genotype probabilities file and the genotype dosage file. We used the mean values of the posterior probabilities estimated for all the individuals in the inference panel.
- 12.
B-allele dosage: Given the posterior genotype probabilities for a SNP (Pr(AA), Pr(AB), and Pr(BB)), the estimated B-allele dosage for each individual is equal to 0 × Pr(AA) + 1 × Pr(AB) + 2 × Pr(BB), which is reported in the genotype dosage file. We used the mean values of the B-allele dosage values of all the individuals in the inference panel.
It is worth mentioning that the posterior probability estimated by the imputation program and the B-allele dosage are highly correlated to predicting the IQS under the statistical correlation analysis. These features will be used in the regression model for the IQS as well as the regression for the observed agreement P_{ o } and the chance agreement P_{ c }. We will show that these 12 features are useful to construct an adequate regression model.
Data preparation
We prepared three data sets to evaluate the performance of our regression models. These data sets contain genotyping results of samples chosen to cover different ethnic backgrounds collected in different disease studies. We selected recent data sets genotyped with advanced platforms that cover a large number of SNPs so that we can flexibly keep those SNPs covered by old, obsolete platforms (with less SNPs probed) and hold out the rest to impute. Meanwhile, since we have their true genotypes, we can use the true genotypes of these SNPs as the gold standard to evaluate imputation quality and regression.
The Merlion Lung Cancer Study 2 DNA [19] and Oral Squamous Cell Carcinoma samples [20] from the NCBI GEO database [21] were used for evaluating the regression model. The Merlion Lung Cancer samples consist of two ethnic populations, East-Asian (EA) and Western-European (WE). Samples were all genotyped on the Affymetrix Genome-Wide Human SNP Array 6.0 platform. This platform contains more than 906,600 SNP probes, including the historical 482,000 SNPs in the Affymetrix GeneChip Human Mapping 500K Array Set. After the preprocessing of raw CEL files, there are 763,252 SNPs reported for the EA population of Merlion Lung Cancer samples, 778,058 SNPs for the WE population of Merlion Lung Cancer samples, and 693,494 SNPs for the oral Squamous Cell Carcinoma samples.
Regression performance evaluation
We designed scenarios to simulate the imputation of missing SNPs in a data set genotyped using an old platform to the large set of SNPs on the Affymetrix SNP 6.0 array. These scenarios involve a training set to construct our regression model in advance. This involves holding out a set of SNPs to impute, evaluating true IQS with known alleles, using the true IQS to train the regression model. Then the trained regression model can be applied to estimate IQS of imputed SNPs in a test set, where a set of SNPs is assumed to have missing genotypes. The design of the scenarios is to create different combinations of the training and test sets and see how the regression performance is affected.
To create both training and test sets, we basically divided the SNPs on the Affymetrix SNP 6.0 array into two sets. One contains those SNPs genotyped in both an old platform and Affymetrix SNP 6.0 array. This set simulates SNPs with "known" genotypes to be used to impute other SNPs. The other contains the remaining SNPs covered only by the Affymetrix SNP 6.0 array. This set simulates "missing" SNPs to be imputed.
Summary of training set composition for different evaluation scenarios
Scenarios | Ethnic population | Samples | from Platform | to Platform |
---|---|---|---|---|
Scenario 1 | Western European | Lung cancer | from Affymetrix 500k | to Affymetrix 500k |
Scenario 2 | Western European | Lung cancer | from Illumina 550k | to Illumina 550k |
Scenario 3 | East Asian | Lung cancer | from Affymetrix 500k | to Affymetrix 500k |
Scenario 4 | East Asian | Lung cancer | from Affymetrix 500k | to Affymetrix 500k |
Summary of test set composition for different evaluation scenarios
Scenarios | Ethnic population | Samples | from Platform | to Platform |
---|---|---|---|---|
Scenario 1 | Western European | Lung cancer | from Affymetrix 500k | to Affymetrix SNP 6.0 |
Scenario 2 | Western European | Lung cancer | from Affymetrix 500k | to Affymetrix SNP 6.0 |
Scenario 3 | Western European | Lung cancer | from Affymetrix 500k | to Affymetrix SNP 6.0 |
Scenario 4 | East Asian | Oral cancer | from Affymetrix 500k | to Affymetrix SNP 6.0 |
In Scenario 2, the generalization performance of our IQS regression model was evaluated when it was trained using "known" and "missing" SNPs covered by platforms different from those to be used in testing. We used the WE lung cancer sample again but used the Illumina 550k array instead of the Affymetrix SNP 6.0 array to choose SNPs. There are 41,304 SNPs of the WE lung cancer sample on the Illumina 550k array. After the regression model is constructed, we then used the same test set created in Scenario 1.
In Scenario 3, our IQS regression model is applied to different ethnic populations. We used the EA lung cancer sample to create the training set, resulting in 37,611 SNPs of the EA lung cancer sample on the Affymetrix 500k array. The regression model constructed by the EA lung cancer samples was used to predict the IQS of SNPs of the WE lung cancer samples as in Scenario 1.
Scenario 4 tests if our regression model can be generalized across samples collected for different disease studies. We used the same training set as in the scenarios above and used the EA Oral Squamous Cell Carcinoma sample as the test set. This test set also simulates imputation from the Affymetrix mapping 500k array to the Affymetrix SNP 6.0 array and consists of 320,172 SNPs.
For all scenarios, we chose the imputation program Beagle. Beagle is based on the Hidden Markov Model (HMM) [22]. To estimate missing alleles, an EM algorithm is adopted to optimize the parameters to fit the HMM model from a given genotyped reference panel [2, 7]. In terms of imputation accuracy, Beagle perform as well as other imputation programs but is known to be more efficient with regard to running time and memory space required [23].
The 1000 Genomes Project samples (August 2010 release) served as the reference panel. As the larger reference panel has developed, researchers have become more confident to combine two studies or extend a specific study on different platforms [23]. We removed those SNPs with MAF less than 1% that usually lead to decreased imputation accuracy [9, 23]. About 2% of SNPs were removed before the imputation. Notably, there are a few SNPs with inconsistent genotyped markers compared to the reference panel. These few SNPs (< 0.01%) will be excluded from the training or test set in order to focus only on the reasonable imputation results.
Results and discussion
Summary of the IQS regression results for each scenario
IQS regression results | ||
---|---|---|
Scenario | Mean Squared Error | Correlation Coefficient |
Scenario 1 | 0.0182 | 0.740 |
Scenario 2 | 0.0174 | 0.748 |
Scenario 3 | 0.0178 | 0.736 |
Scenario 4 | 0.0197 | 0.751 |
The best performance was accomplished in Scenario 2, where the regression model was trained with a set of SNPs derived from different platforms from the test, suggesting that training with a wider variety of SNPs might allow the model to generalize better. The worst performance was from Scenario 4, where samples from studies of different diseases were tested. Nevertheless, the performance difference was not significant.
Summary of the P_{ o } regression results for each scenario
P_{ o }regression results | ||
---|---|---|
Scenario | Mean Squared Error | Correlation Coefficient |
Scenario 1 | 0.00248 | 0.840 |
Scenario 2 | 0.00249 | 0.838 |
Scenario 3 | 0.00256 | 0.835 |
Scenario 4 | 0.00301 | 0.831 |
Summary of the P_{ c } regression results for each scenario
P_{ c }regression results | ||
---|---|---|
Scenario | Mean Squared Error | Correlation Coefficient |
Scenario 1 | 0.00062 | 0.990 |
Scenario 2 | 0.00072 | 0.988 |
Scenario 3 | 0.00071 | 0.989 |
Scenario 4 | 0.00099 | 0.984 |
Conclusion
We propose a ν-SVR based approach to the estimation of the true IQS of imputations of SNPs with unknown true genotypes. We show that our regression model generalizes equally well across SNP selections by different platforms and across different ethnic groups and disease populations. The model performed particularly well for predicting the true chance agreement of imputation. We also showed that the estimated IQS can be used to filter false positive associations in a GWAS to some extent. The results suggest that it is feasible to apply a regression model to predict the true IQS.
Our future work includes an effort to extend the feature set to improve the regression performance for predicting P_{ o } and the IQS and to pool together a wide variety of data sets including different SNPs and populations as the training examples so that one model can be used to estimate the IQS for all imputations. When the model is sufficiently robust, our long-term goal is to impute to the same size all genotype data in repositories of GWAS data (to as large as the most advanced platforms) and apply this regression model to attach an estimated IQS to all imputations in addition to the posteriori probability from the imputation program and make the results available in the public domain.
Declarations
Acknowledgements
This work was supported in part by NIMH/NIH Grant Number MH068457 (CGSMD).
This article has been published as part of BMC Proceedings Volume 6 Supplement 7, 2012: Proceedings from the Great Lakes Bioinformatics Conference 2012. The full contents of the supplement are available online at http://www.biomedcentral.com/bmcproc/supplements/6/S7.
Authors’ Affiliations
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