Volume 5 Supplement 3
Proceedings of the 14th European workshop on QTL mapping and marker assisted selection (QTL-MAS)
Association analyses of the MAS-QTL data set using grammar, principal components and Bayesian network methodologies
- Burak Karacaören^{1}Email author,
- Tomi Silander^{2},
- José M Álvarez-Castro^{1, 3},
- Chris S Haley^{1, 4} and
- Dirk Jan de Koning^{1}
https://doi.org/10.1186/1753-6561-5-S3-S8
© Karacaören et al; licensee BioMed Central Ltd. 2011
Published: 27 May 2011
Abstract
Background
It has been shown that if genetic relationships among individuals are not taken into account for genome wide association studies, this may lead to false positives. To address this problem, we used Genome-wide Rapid Association using Mixed Model and Regression and principal component stratification analyses. To account for linkage disequilibrium among the significant markers, principal components loadings obtained from top markers can be included as covariates. Estimation of Bayesian networks may also be useful to investigate linkage disequilibrium among SNPs and their relation with environmental variables.
For the quantitative trait we first estimated residuals while taking polygenic effects into account. We then used a single SNP approach to detect the most significant SNPs based on the residuals and applied principal component regression to take linkage disequilibrium among these SNPs into account. For the categorical trait we used principal component stratification methodology to account for background effects. For correction of linkage disequilibrium we used principal component logit regression. Bayesian networks were estimated to investigate relationship among SNPs.
Results
Using the Genome-wide Rapid Association using Mixed Model and Regression and principal component stratification approach we detected around 100 significant SNPs for the quantitative trait (p<0.05 with 1000 permutations) and 109 significant (p<0.0006 with local FDR correction) SNPs for the categorical trait. With additional principal component regression we reduced the list to 16 and 50 SNPs for the quantitative and categorical trait, respectively.
Conclusions
GRAMMAR could efficiently incorporate the information regarding random genetic effects. Principal component stratification should be cautiously used with stringent multiple hypothesis testing correction to correct for ancestral stratification and association analyses for binary traits when there are systematic genetic effects such as half sib family structures. Bayesian networks are useful to investigate relationships among SNPs and environmental variables.
Background
It has been shown that ignoring genetic relationships among cases and controls may lead to false positives in genome wide association analyses (GWAS). Genome-wide Rapid Association using Mixed Model and Regression, GRAMMAR, (Aulchenko et al, 2007) approach is a one solution based on correction of quantitative trait for both polygenic and fixed effects. Another approach, introduced by Price et al (2006), uses principal components loadings (PCL) as covariate in linear regression models for detecting and correcting ancestral stratifications for categorical traits in GWAS.
GWAS analyses result in a list of significant SNPs. Some of these SNPs will be in linkage disequilibrium (LD) due to the dense set of markers and this may lead to collinearity among these SNPs. Collinearity among genotype scores could raise problems when applying model selection procedures and different solutions have been proposed from non parametric methods to selective algorithms (Wang and Abbott, 2008). Wang and Abbott (2008) suggested using a principal component regression (PCReg) approach to break the collinearity among marker genotypes using top principal components loadings (PCL) as covariates in the linear regression model. Pant et al (2010) extended the PCReg approach to the categorical traits via logistic regression and model selection strategies.
Most of the GWAS studies do not take into consideration the possible relations among SNPs and/or with other explanatory variables. Bayesian networks are models that present statistical dependencies and independencies in the joint probability distribution of the data. As such they do not state causality, but it is certainly possible to speculate what kind of causal mechanisms would be compatible with the observed dependencies and independencies. Rodin et al (2005) used Bayesian networks to do joint inference on marker variation in the human APOE gene and plasma apolipoprotein E levels. Sebastiani et al (2005) used Bayesian networks in association studies.
The main aim of this study was to apply GRAMMAR, Bayesian Network and principal component stratification models to QTL-MAS 2010 dataset.
Methods
Genome-wide rapid association using mixed model and regression
In the first step of the GRAMMAR analysis, we estimated the heritabilities and residuals for the quantitative trait using an animal model as was implemented in Asreml (http://www.vsni.co.uk/software/asreml);
y = Xb + Za + e (1)
For the random effects, it is assumed that A is the additive genetic relationship matrix for the animals; I is an identity matrix, is the additive genetic variance and is the residual variance. In the second step, assuming a single SNP model for the quantitative trait, we could detect the most significant SNPs using the following model:
y=Xf + η + e (2)
where y represents vector of n observations (residuals from (1)), η is intercept, X is a design matrix relating observations with f regression coefficients vector to be estimated, e is a vector of residuals assumed to be normally distributed. We applied GRAMMAR (Aulchenko et al, 2007) with 1000 permutation to detect most significant SNPs for quantitative trait using residuals obtained (1) and used in (2) as response variable.
Principal components analyses
Principal components analyses can be used to decompose the genomic matrix into a set of new orthogonal variables which account for the total variance of the original variables (Everitt et al., 2001) in decreasing proportions. For the binary trait, we used principal component stratification (Price et al, 2006) methodology to account for ancestral stratification in the QTL-MAS2010 dataset, as was implemented in SAS and JMP Genomics software (SAS institute, Inc, Carey, NC, USA) version 9.1. In order to take LD among significant markers into account for GRAMMAR and principal component stratification approaches we applied principal component analyses with 21 (PCL) as covariate (about 80% of variance explained) for the quantitative trait and 20 PCL as covariate (about 75% of variance explained) for the binary trait in regression models (Minitab, Ver 14).
Bayesian network
For data D of n-dimensional i.i.d. data vectors the formula above allows us to calculate the probability P(D | G, Θ). More interestingly, in a Bayesian setting, under certain technical assumptions, after giving a prior distribution for the parameters Θ, one may calculate the marginal likelihood P(D | G,α), where α denotes the hyperparameters for the prior distribution of the Θ. This allows us to compare Bayesian network structures by their posterior probability P(G | D,α) α P(D | G,α)P(G) (Heckermann et al. 1995). It is well known that finding the most probable Bayesian network structure is an NP-hard problem (Chikering 2002). Therefore it is customary to resort to search heuristics such as a local greedy search. However, it has been shown that the most probable forest structured Bayesian network (i.e. a network in which each variable has at most one parent) can be found in quadratic time with respect to number of variables n (Heckermann et al. 1995).
We used the significant markers found from GRAMMAR and principal component approaches to train the Bayesian network. We learned both general Bayesian network and Bayesian Forests using different search algorithms to compare the results with LD measures. Details of the LD measures used in this paper could be found in Devlin and Risch (1995).
Results
Quality Control
We excluded 263 SNPs due to minor allele frequency <1%, leaving 9768 SNPs in the analyses. We excluded 8 individuals with too high IBS (Identity By State) (>95%) leaving 2318 individuals in the dataset. Normality for the quantitative trait was confirmed by Kolmogorow Smirnow test, P > 0.150. Based on an animal model (1) we estimated heritabilities as 0.44 (±0.05) for the binary trait and 0.58 (±0.12) for the quantitative trait.
Analysis of binary trait
We used 20 PCL to take possible ancestral stratification into account for the binary trait. Visual inspection of the scree plot showed that the sharpest reduction was obtained from the first 10 principal components. We detected the top 109 SNPs based on local FDR (Strimmer, 2008a) (p<0.0006). In order to take linkage disequilibrium into account we additionally applied PCReg with normal and logit functions. Using the first 20 PCL as covariate, we applied PCReg to 109 markers with a logit function, and obtained the top 50 SNPs from this approach. We also investigated loading plots for the top SNPs. Although some clusters were found related with location of the SNPs and LD among them, this was not observed consistently for the entire genome (Additional File 1). We mapped 5 QTL’s correctly with 0.33Mb average distance from the simulated QTL. Although top markers such as 5488 or L4483 were detected by the model, 41 QTL showed an average distance of 5.5 Mb from the nearest real QTL and could be considered false positives. This suggests that under the strong systematic genetic effects (as such as a half-sib family structure) more stringent multiple hypothesis testing correction procedures should be used.
Analysis of quantitative trait
Bayesian network
Comparison of linkage disequilibrium measures with general Bayesian Network arc strengths.
Marker1 | Marker2 | Chi | P(Chi) | D | CorrCoeff | Dprime | Delta | PropDiff | YulesQ | ARC | exp(ARC) |
---|---|---|---|---|---|---|---|---|---|---|---|
A8111 | A9100 | 692.12 | 1.50x10^{-152} | 0.09 | 0.55 | 0.87 | 0.88 | 0.71 | 0.95 | 293.53 | 3.01x10^{127} |
A8363 | A9100 | 516.77 | 2.10x10^{-114} | 0.08 | 0.47 | 0.99 | 0.99 | 0.66 | 0.99 | 71.68 | 1.35x10^{31} |
A8111 | A8363 | 548.72 | 2.40 x10^{-114} | 0.11 | 0.49 | 0.64 | 0.51 | 0.45 | 0.82 | 519.43 | 3.85x10^{225} |
A8111 | A8351 | 2318 | 1.70 x10^{-236} | 0.16 | 0.68 | 0.98 | 0.63 | 0.63 | 0.99 | 694.50 | 4.14x10^{301} |
A8035 | A8329 | 1668.98 | 0 | 0.21 | 0.85 | 0.97 | 0.84 | 0.83 | 1.00 | 232.66 | 1.10x10^{101} |
A8329 | A8351 | 20.12 | 7.27 x10^{-6} | -0.02 | -0.09 | -0.11 | -0.19 | -0.09 | -0.19 | 240.85 | 3.98x10^{104} |
Comparison of Bayesian Forest estimates with Linkage Disequilibrium estimates.
Marker1 | Marker2 | ChiSq | ProbChi | D | CorrCoeff | Dprime | Delta | PropDiff | YulesQ | ARC | Exp(ARC) |
---|---|---|---|---|---|---|---|---|---|---|---|
A599 | A613 | 1567.399 | 0 | 0.09 | 0.82 | 0.95 | 0.74 | 0.74 | 1.00 | 850.271 | NA* |
A599 | A5603 | 117.2745 | 2.50 x10^{-27} | 0.04 | 0.22 | 0.60 | 0.15 | 0.14 | 0.66 | 80.5 | 9.13 x10^{34} |
A3102 | A3105 | 1916.852 | 0 | 0.20 | 0.91 | 1.00 | 1.00 | 0.94 | 1.00 | 1668.336 | NA* |
A3102 | A3444 | 128.9518 | 6.95 x10^{-30} | 0.03 | 0.24 | 0.66 | 0.67 | 0.46 | 0.76 | 80.14 | 6.37 x 10^{34} |
Pearson correlations between General Bayesian network (A) and Bayesian Forest (B) and linkage disequilibrium measures.
A | D | Correlation Coefficients | D Prime | Yules Q |
---|---|---|---|---|
Correlation Coefficients | 0.961 | |||
D prime | 0.689 | 0.776 | ||
Yules Q | 0.719 | 0.809 | 0.950 | |
ARC | 0.692 | 0.726 | 0.483 | 0.456 |
B | D | Correlation Coefficients | D Prime | Yules Q |
Correlation Coefficients | 0.882 | |||
D prime | 0.434 | 0.601 | ||
Yules Q | 0.537 | 0.697 | 0.900 | |
ARC | 0.892 | 0.915 | 0.576 | 0.569 |
Estimation of SNPs effects
For quantitative trait we estimated the SNPs effects with linear models. We used residuals from model (1) as response variable in a linear model. When we used phenotypes as response variable linear model tend to overestimate the total explanatory variation. We estimated QTL variance for the top marker (5488) as 7.7 % and 2.9 % using linear models with phenotypic and residual values, respectively. This QTL was simulated with 4.49 % variance suggesting that using residuals gave more correct estimates. When residuals are not normally distributed, orthogonal models are robust compared with a linear model from deviation of normality (Sarabia et al, 1997).
Conclusions
When cases and controls have genetic relations, GRAMMAR could efficiently incorporate the information regarding random genetic effects. Principal component stratification could be used to correct for ancestral stratification and association analyses for binary traits although if there is systematic genetic effects stringent multiple hypothesis test corrections should be used. Bayesian networks are useful to investigate relationships among SNPs and environmental variables. Although a learned network does not have to show causal relationships, it is still informative and creates hypotheses based on interactions among SNP’s.
Declarations
Acknowledgements
The authors thank to anonymous reviewers for useful comments. BK, DJK, and CH grateful for funding from BBSRC through the GridQTL project (BBSB1695X), and SABRE (EC contract number FOOD-CT-2006-01625). CSH was funded by a MRC core grant. The contributions of DJK and CSH were funded in part by a BBSRC Institute Strategic Programme Grant. JAC acknowledges funding from grant JC2009-oo239 from the Spanish Ministry of Science and an IPP contract from the autonomous government Xunta de Galicia.
This article has been published as part of BMC Proceedings Volume 5 Supplement 3, 2011: Proceedings of the 14th QTL-MAS Workshop. The full contents of the supplement are available online at http://www.biomedcentral.com/1753-6561/5?issue=S3.
Authors’ Affiliations
References
- Aulchenko SY, de Koning DJ, Haley CS: Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis. Genetics. 2007, 177: 577-585. 10.1534/genetics.107.075614.PubMed CentralView ArticlePubMedGoogle Scholar
- Chickering D: Learning Bayesian networks is NP-complete. Learning from Data: Artificial Intelligence and Statistics V. Edited by: Fisher D, Lenz H. 1996, Springer-Verlag, 121-130.View ArticleGoogle Scholar
- Devlin B, Risch N: A comparison of linkage disequilibrium measures for fine scale mapping. Genomics. 1995, 29: 311-322. 10.1006/geno.1995.9003.View ArticlePubMedGoogle Scholar
- Everitt SB, Landau S, Leese M: Cluster analysis. 2001, ArnoldGoogle Scholar
- Heckerman D, Geiger D, Chickering D: Learning Bayesian networks: The combination of knowledge and statistical data. Machine Learning. 1995, 20 (3): 197-273.Google Scholar
- Pearl J: Probabilistic Reasoning in Intelligent Systems: Networks of Plausible Inference. 1988, Morgan Kaufmann Publishers, San Mateo CAGoogle Scholar
- Pant SD, Schenkel FS, Verschoor CP, You Q, Kelton DF, Moore SS, Karrow NA: A principal component regression based genome wide analysis approach reveals the presence of a novel QTL on BTA7 for MAP resistance in holstein cattle. Genomics. 2010, 95: 176-182. 10.1016/j.ygeno.2010.01.001.View ArticlePubMedGoogle Scholar
- Price AL, Patterson NJ, Robert MP, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nature Genetics. 2006, 38: 904-909. 10.1038/ng1847.View ArticlePubMedGoogle Scholar
- Rodin AS, Boerwinkle E: Mining genetic epidemiology data with Bayesian networks 1: Bayesian networks and example application. Bioinformatics. 2005, 21: 3273-3278. 10.1093/bioinformatics/bti505.PubMed CentralView ArticlePubMedGoogle Scholar
- Sarabia LA, Ortiz MC, Tomas X: Performance of the orthogonal least median squares regression. Anal Chimica Acta. 1997, 348: 11-18. 10.1016/S0003-2670(97)00142-6.View ArticleGoogle Scholar
- Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH: Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet. 2005, 37: 435-440. 10.1038/ng1533.PubMed CentralView ArticlePubMedGoogle Scholar
- Strimmer K: A unified approach to false discovery rate estimation. BMC Bioinformatics. 9: 303-10.1186/1471-2105-9-303.Google Scholar
- Wang K, Abbott D: A principal components regression approach to multilocus genetic association studies. Genet Epidemiol. 2008, 32: 108-118. 10.1002/gepi.20266.View 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.