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rPCMP: robust pvalue combination by multiple partitions with applications to ATACseq data
BMC Systems Biology volume 12, Article number: 141 (2018)
Abstract
Background
Evaluating the significance for a group of genes or proteins in a pathway or biological process for a disease could help researchers understand the mechanism of the disease. For example, identifying related pathways or gene functions for chromatin states of tumorspecific T cells will help determine whether T cells could reprogram or not, and further help design the cancer treatment strategy. Some existing pvalue combination methods can be used in this scenario. However, these methods suffer from different disadvantages, and thus it is still challenging to design more powerful and robust statistical method.
Results
The existing method of Group combined pvalue (GCP) first partitions pvalues to several groups using a set of several truncation points, but the method is often sensitive to these truncation points. Another method of adaptive rank truncated product method(ARTP) makes use of multiple truncation integers to adaptively combine the smallest pvalues, but the method loses statistical power since it ignores the larger pvalues. To tackle these problems, we propose a robust pvalue combination method (rPCMP) by considering multiple partitions of pvalues with different sets of truncation points. The proposed rPCMP statistic have a threelayer hierarchical structure. The innerlayer considers a statistic which combines pvalues in a specified interval defined by two thresholds points, the intermediatelayer uses a GCP statistic which optimizes the statistic from the inner layer for a partition set of threshold points, and the outerlayer integrates the GCP statistic from multiple partitions of pvalues. The empirical distribution of statistic under null distribution could be estimated by permutation procedure.
Conclusions
Our proposed rPCMP method has been shown to be more robust and have higher statistical power. Simulation study shows that our method can effectively control the type I error rates and have higher statistical power than the existing methods. We finally apply our rPCMP method to an ATACseq dataset for discovering the related gene functions with chromatin states in mouse tumors T cell.
Background
Genetic association analysis has been widely used to identify many associated genes with human complex diseases [1, 2]. In recent decades, the advances on biological techniques have made it possible to collect massive amounts of highthroughput datasets such as SNP data and gene expression data, which are often high dimensional, and have a large number of variables and a relatively small number of samples. A typical problem is to find out single nucleotide polymorphisms (SNPs) or genes related to corresponding diseases. Singlemarker analysis could be done by twosample test on each variable such as Fisher’s exact test, or Chisquared test for categorical datasets, and twosample ttest or Wilcoxon test for numerical datasets. However, a major disadvantage of singlemarker based methods is that they do not consider the joint effects of multiple genetic variants which may have weak or moderate signals individually. The joint use of information from multiple markers may be more effective to reveal association between a genomic region and a trait than single marker analysis. In this scenario, genebased, genesetbased and pathwaybased association tests provides a more powerful way in addition to the more widely used single marker association analysis. For example, one may want to test using SNP datasets whether a gene, including several or many SNPs, is significantly associated with a trait, or want to test using highthroughput gene expression datasets whether a biological pathway, including several genes, is significantly associated with a trait.
One method to detect the association between a gene, which may hosts a lot of SNPs, or a biological pathway, which may have many genes, and human complex diseases in large scale genetic studies is using the framework of logistic regression to learn the odd ratios of SNPs. However, this may not work due to the highdimensional problem. Especially when the SNPs are in high linkage disequilibrium, the solution is not stable. Gene set enrichment analysis algorithm [3] has been proposed for the identification of disease related pathways by measuring the overrepresentation of diseasegene associations within a given pathway compared to a list of reference genes. The underlying null hypothesis is that the set of genes in a given pathway has no enrichment of association signals compared to the rest. In contrast, in this manuscript, we focus on testing for the effect of a specific pathway/gene set without reference to any larger gene list. The underlying global null hypothesis is that there is no association of the disease with any of the genes in the given gene set. A more promising strategy is to use univariate test which constructs marginal test for each variable first and then combine the pvalues together by pvalue combination methods to accumulate marginal signals.
The earliest method to combine individual pvalues is Fisher’s combined probability test (FCT) [4], which is popularly used in many applications [5–7] or taken as part of the statistic in other more complicated pvalue combination methods such as [8–10]. FCT basically combines m independent pvalues into a test statistic, which is proved to follow a chisquare distribution with 2m degrees of freedom under null hypothesis. When the pvalues are not independent, empirical distribution is suggested to use, otherwise the type I error rates may be inflated [8]. However, FCT method may lose power when the number of individuals in the gene set is large, or most of the individuals are not significant. Zaykin et. al. [8] propose a truncated product method(TPM) which takes the product of only those pvalues less than some specified cutoff value ξ and to evaluate the probability of such a product under the null hypothesis. 0.05 is usually adopt as the cutoff in practice. Different from [8], Dudbridge et al. [9] use an alternative strategy to take rank truncated product (RTP) of the K most significant pvalues as the statistic for the testing. However, the two methods of TPM and RTP are both sensitive to the parameters ξ or K, and an inappropriate truncation point can have a detrimental effect on the power. In order to overcome this problem, especially when there are a large number of pvalues to be combined, [11] proposed adaptive rank truncated product method (ARTP) to optimize the selection of the truncation point with a set of candidates. The defined statistic is the minimum empirical pvalue observed at different truncation points.
An alternative method for testing the overall null hypothesis is tail strength (TS) method. This TS test statistic is a function of ordered pvalues [12], which has an asymptotic normal distribution with mean of 0 and variance of 1/m under the null hypothesis if the mpvalues are independent. Similar to [8, 13] defines a new truncated tail strength (TTS) statistic for testing the null hypothesis by removing pvalues larger than a cutoff. The TTS statistic appears to have good properties, especially when there are a large number of independent tests in one dataset.
More recently, [14] adopts a sequential method for combining information from correlated pvalues and presents the SEQ algorithm for correlated pvalues. Hu et al. [10] defines a GCP statistic by using two functions log and the cumulative distribution function of two degrees of freedom to combine the pvalues and show more power than FCT when these pvalues are correlated and few pvalues show significances. In GCP method, pvalues are divided to several groups first by thresholds, and then constructed into a statistic with each group. However, when the number of individual tests is large, the performance of GCP is very sensitive to the selection of thresholds.
In this work, we propose a more robust statistical method called rPCMP to improve GCP method, by using multiple partitions of pvalues. Borrowing the idea from ARTP, which takes several truncation points, our rPCMP takes several sets of thresholds to divide pvalues to groups for several times. The defined rPCMP havs threelayer structure, which could be empirically estimated by a permutation procedure. Extensive simulations studies show that our proposed rPCAMP test method perform more powerful than some existing pvalue combination methods, with low type I error rates. Our method is finally applied to a ATACseq dataset, to find the related gene functions for chromatin states in mouse tumor cells. The proposed method succeeds in detecting significant gene functions for tumorspecific T cell dysfunction and reprogramming.
Methods
Problem statement
Suppose we have gene expression dataset X∈R^{m×N} for m genes g_{1},⋯,g_{m} and N samples, and also a phenotype y∈R^{N}. The gene set S={g_{1},⋯,g_{m}} is often predefined by a biological pathway or a group of genes with the same gene function. For each gene i, a single null hypothesis of interest could be H_{0i}: the ith gene is not associated with the phenotype, i=1,⋯,m. We could calculate mpvalues {p_{1},⋯,p_{m}} by a certain test statistic such as twosample ttest or Wilcoxon test, which tests H_{0i} to determine whether the corresponding single gene is significantly associated with the phenotype or not. Our goal is to test an overall null hypothesis H_{0}: no gene in set S is significantly associated with the phenotype, and thus evaluate the association of the whole gene set S and the phenotype by calculating a group pvalue for S.
The methods of FCT, TPM, ARTP and GCP
Fisher’s combination test (FCT) [4]
Suppose the mpvalues are generated from m statistical tests based on m normally distributed random variables, say, the mth row of X, X_{m}. Fisher showed that for independent pvalues, the statistic
follows a χ^{2} distribution with 2m degrees of freedom. Based on this theoretical result, a hypothesis testing can be performed to calculate a combined pvalue. If the original pvalues are independent, a permutation procedure could be used to empirically estimate the null distribution and thus calculate the combined pvalue.
Truncated product method (TPM) [8]
Truncated product method uses the product of only those pvalues smaller than a specified threshold ξ. The corresponding statistic is defined as
where I() is an indicator function, I(p_{i}≤ξ)=1 if p_{i}≤ξ and I(p_{i}≤ξ)=0 otherwise.
Adaptive rank truncated product method (ARTP) [11]
ARTP makes use of multiple candidate truncation integers K_{1},⋯,K_{L} to adaptive combine the the smallest pvalues. The m pvalues are first ordered as p_{(1)}≤p_{(2)}≤⋯≤p_{(m)}, where p_{(k)} is the kth smallest pvalue. A statistic which combines the smallest K_{l}pvalues are defined by
Let s_{l} be the pvalue corresponding to W_{l}, which could be estimated by a permutation procedure. The statistic based on minimum pvalue can be defined as
The adjusted combined pvalue corresponding to MinP is estimated by the permutation procedure.
Group combinedpvalue (GCP) [10]
Different from ARTP, which combines the smallest pvalues using different truncation integers, Group combined pvalue (GCP) method considers the pvalues in different specified intervals. Given J cutoff values 0<ξ_{1}<ξ_{2}<⋯<ξ_{J}<1, GCP defines a statistic
where ξ_{0}=0 and F_{j} is the cumulative distribution function of \({\sum }_{i=1}^{m}2\ln p_{i}I_{\{\xi _{j1} < p_{i} \leq \xi _{j} \}}\) for j=1,2,⋯,J. The permutation procedure is also used to estimate the empirical pvalue corresponding to GCP.
Combining pvalues by multiple partitions
In GCP method, it is unclear how to choose cutoff values for calculating the group combined pvalues. Note that one choice of these cutoffs actually mean a partition of the mpvalues. Different partitions of these pvalues will result in different testing results. In this work, we aim to propose a robust method, which accounts for multiple partitions of the pvalues. Suppose we have L partitions of the mpvalues, say, \(0=\xi ^{l}_{0}<\xi ^{l}_{1}<\xi ^{l}_{2}<\xi ^{l}_{3}<\cdots <\xi _{J_{l}}^{l}<1, l =1,\cdots,L\). We borrow the ideas of both ARTP and GCP, and define a rPCMP statistic by integrating the multiple partitions of the pvalues:
where F_{j,l} is the cumulative distribution function of \(\thinspace 2{\sum }_{i=1}^{m} \ln p_{i}I_{\left \{\xi ^{l}_{j1} < p_{i} \leq \xi ^{l}_{j}\right \}}\), and G_{l} is the cumulative distribution function of
Note that there are three layers of the rPCMP statistic. The innerlayer distribution F_{j,l} depends on both the partition l and the cutoff values \(\xi ^{l}_{j1}\) and \(\xi ^{l}_{j}\), the intermediatelayer G_{l} depends only on the thresholds of the lth partition, and outerlayer statistics integrate all the L multiple partitions. ARTP statistic takes twolayer distributions, but both the two layers are different from rPCMP. The threelayer structure of the rPCMP statistic is shown in Fig. 1.
The distribution of the threelayer rPCMP statistic under the overall null hypothesis could be both estimated by generating permutation pvalues under null distribution. Therefore, to obtain the adjusted pvalue for the defined statistic rPCMP, we need a threelevel permutation procedure [15] with the inner level for estimating F_{j,l}, intermediatelayer for estimating G_{l}, and the outerlayer for rPCMP with multiple partitions. However, this would be computationally expensive if m is relatively large. Thus a singlelayer permutation is used to determine the significance level for rPCMP, which borrows techniques originally designed for gene expression analysis [16]. By this singlelayer permutation procedure, we first calculate pvalues \(p^{0}_{1},\cdots,p^{0}_{m}\) for each test on the null hypothesis based on the observed data {X,y}. We then generate B permuted datasets {X,y_{b}} by randomly permuting the phenotype y to be y_{b}, where 1≤b≤B, under the null hypothesis. Based on these B permuted datasets, we can calculate pvalues \(p^{b}_{1},\cdots,p^{b}_{m}\). By using these pvalues, we can apply the rPCMP algorithm to obtain the adjusted pvalues for the rPCMP statistic. The detailed steps are shown in the algorithm rPCMP.
Results
Simulation datasets
We generate N columns of X∈R^{m×N} by multivariate normal distribution with zero mean and a covariance matrix Σ∈R^{m×m}. For independent case, where genes are assumed to be independent, we just set Σ to be an identical matrix. For dependent case, we set Σ_{ij}=ρ^{i−j}, where the parameter ρ is chosen from the set {0,0.1,0.2,0.3}. The number of genes m is chosen from {100,200,300,400,500}, and the sample size N is chosen as 100. We further generate y∈R^{N} by the following procedure. We first randomly select T_{1} rows from X, which are assumed as the related genes, and then randomly generate T_{2} row vectors by standard normal distribution. y is generated by the linear combination of these T=T_{1}+T_{2} vectors, with the same coefficient 1/T. In our experiments, we fix T=30 and vary T_{1} from 1 to 30. Note that T_{1} is the number of related genes in X. The dataset {X,y} depends on three parameters ρ,m and T_{1}.
Simulation results
For all methods except FCT, there are parameters to be set up. For TPM method, we use 0.5 as the cutoff for all experiments. For ARTP method, the truncation integers are set to be 1 to 10 in all experiments. For GCP, we use the best parameter [0.001, 0.05] suggested by [10]. In our method, 5 groups parameters are used together in all experiments from the sets {[0.01, 0.1], [0.001, 0.05], [0.01, 0.05], [0.001, 0.01, 0.1],[0.001, 0.01, 0.05]}, which are also used in [10].
For each simulation dataset {X,y}, we first compute mpvalues for the m genes by Student’s t test, and then B=1000 permuted ys are used to compute Bpvalues for each gene. We use typeI error and power to measure the performance of the baseline methods and our method. To estimate the typeI error, we set T_{1}=0, calculate 1000 group pvalues by randomly generating 1000 ys. The typeI error is estimated by the proportion of group pvalues less than 0.05 among these 1000 values. To estimate the power, we randomly select T_{1}≥1 rows of X for 1000 times and thus can generate 1000 ys. With each of these ys, we could perform different methods to calculate a group pvalue. The power for the method could then estimated by the proportion of group pvalues less than α=0.05.
We report the Type I error rates in Table 1 by different methods for m∈{100,200,300,400,500} and ρ∈{0,0.1,0.2,0.3}. We can see that all methods could obtain very small type I error rates with slight differences.
In Fig. 2, we show the change of power with T_{1} varied from 1 to 30, for m=300 and different choices of ρ=0,0.1,0.2,0.3. We can see that the four subfigures show the advantage of our rPCMP over all other methods. To account for the overall performance for different T_{1}, we compute further an average area under curve (AAUC) defined as the area under the power curve divided by 30. In Table 2, we report the AAUCs for different m∈{100,200,300,400,500} and ρ∈{0,0.1,0.2,0.3}. We can see that our method performs the best for almost all the cases.
To check the robustness of our rPCMP on the number of partitions L, we remove each partition set from the partition sets {[0.01, 0.1], [0.001, 0.05], [0.01, 0.05], [0.001, 0.01, 0.1],[0.001, 0.01, 0.05]}(denoted by set0) in turn to generate 5 new parameter setting named set1, set2, set3, set4 and set5. Note that these five parameter settings all have L=4 partition sets. In Fig. 3, we show the power of rPCMP computed by average area under curve for each ρ with different m, where ρ varies from the set of {0,0.1,0.2,0.3} and m is selected from the set of {100,200,300,400,500}. We can see that our method can perform stably in all cases.
Demonstration of threelayer statistic of rPCMP
Figure 4 demonstrates the threelayer structure of rPCMP statistic by a simulation study with m=300, T=30, ρ=0. The top layer shows the empirical distributions of F_{j,l} for the jth group in lth partition. Each F_{j,l} could result in a pvalue, shown in title of each subfigure by only choosing the individual pvalues in the corresponding interval, We can see that these pvalues are very unstable, and this implies that a statistic combining individual pvalues in a specified interval is very sensitive to the interval parameters. The secondlayer in the figure shows the empirical distribution of G_{l}, for the lth partition. Each G_{l} actually integrates the information of \(\phantom {\dot {i}\!}F_{1,l},\cdots,F_{J_{l},l}\) from the toplayer. Note that the pvalues obtained by G_{l} is still unstable, which may have large pvalues for some ls, and small pvalues for other ls. For the thirdlayer of the figure, rPCMP integrates the optimized information from the secondlayer of G_{l}, and thus makes the result stable.
Applications for identifying related pathways for tumorspecific T cell dysfunction and reprogramming
Dysfunctional tumorspecific CD8 T cells (TST) in solid tumors allow tumors to progress. Immune checkpoint blockade and adoptive T cell therapy has been successfully used in subset of cancer patients, and this shows great potential of TST. However, it is still a problem how to predict which patients will respond to therapy, and it has important implications for cancer immunotherapy to study the epigenetic regulation of T cell dysfunction and therapeutic reprogrammability. Schietinger et al. [17] points out that TST dysfunciton is initially reversible but ultimately becomes irreversible, even after removal of dysfunctional T cells from the tumor. In the study of [18], “Assay for Transposase Accessible Chromatin using Sequence” (ATACSeq) [19] was used to assess genomewide chromatin accessibility changes during Tcell differentiation in tumors compared to acute infection. T cells in mouse tumors are shown in [18] to differentiate through two discrete chromatin states: a plastic dysfunctional state from which T cells can be rescued, and a fixed dysfunctional state in which the cells are resistant to reprogramming. In their study, some membrane proteins such as CD38, CD101, CD30L, CD5, TCF1, IRF4, BCL2, CD44,PD1, LAG3 and CD62L are identified as related to the two chromatin states. In this application, we aim to use ATACSeq data to identify related gene functions, which are sets of genes, associated with Tcell dysfunction and reprogramming.
The preprocessed ATACseq dataset for mouse is downloaded from the Gene Expression Omnibus with GEO Series accession number GSE89308. Totally 16917 genes are assigned in the ATACseq data. The collected 22 mouse samples are labeled using their plastic or fixed dysfunctional chromatin states identified in [18], i.e., they are labeled as 1 for L5 and L7 representing the chromatin remodelling occurred by day 5 and 7, and labeled as 0 for L14,L21,L28,L35 and L60 representing chromatin remodelling occurred by day 14, 21, 28, 35 and 60. We also collect mouse gene ontologies(GO) from http://baderlab.org/GeneSets, and select 2446 GO terms with five to ten genes to perform the analysis.
We apply our rPCMP method to calculate the group pvalues for all these GO terms, with the same parameters \(\xi _{l}^{j}\) as in the simulation study, and permutation time B=10,0000. We identify 13 GO terms shown in Table 3 with smallest group pvalues as the related gene functions to tumorspecific T cell dysfunction and reprogramming. Some of these identified gene functions are related with immune system, including GO:0033007, GO:0002322, GO:0002923, GO:0002921, GO:0002279 and GO:0061081. The gene set GO:0033007 includes immune genes CD300a and CD84, GO:0002322 includes CD180, GO:0002923 includes CD55, GO:0002921 includes CD59b, CD46 and CD59a, GO:0002279 includes CD300a, and GO:0061081 includes CD74,CD36. These genes are highly related to the identified CD family genes in [18]. Besides, another gene set GO0030855 also includes CD family genes CD37. We also found that other gene sets include gene TCF1, which is another name of TCF7, and gene BCL2. These two genes are also identified in [18]. The evidence shows that by our results are well supported by the results in [18], which identifies several CD family genes as related to the chromatin states.
To show the better performance of rPCMP than GCP, we also apply GCP to obtain the group pvalues for all these GO terms with the best cutoff interval suggested by [10]. The results show that GCP could only find five GO terms involving the genes identified by [18], or related to immune systems. These GO terms include GO:0002765, GO:0002826, GO:0002857, GO:0042092 and GO:0002566. Among them, GO:0002826 and GO:0002566 are also discovered by our rPCMP, and only GO:0002857 contains CD family genes while the others don’t have both CD family and BCL2 family genes. This futher shows that rPCMP outperforms GCP on this biological application.
Discussion
The rPCMP proposed in this work shows robustness and higher statistical power than other existing pvalue combination methods in most scenarios of the simulation studies. This is highly expected since the compared methods except ARTP only take a partition of pvalues, while rPCMP takes several partitions into account for combining pvalues. Although ARTP also takes different truncation points, it neglects the larger individual pvalues, and thus loses some information. Our rPCMP extends the pvalue combination technique of GCP by dividing pvalues to several groups for multiple times, and grouping them first in threshold level and then in partition level. The strategy optimizes the different partitions and and accumulates the advantages from different partitions to improve the power of test significantly, and thus is more robust than GCP with a fixed partition. Simulations studies show that rPCMP outperform other methods in most scenarios, and the applications to ATACSeq data further demonstrate its good performance.
The success of rPCMP mostly comes from its threelayer statistical structure, which makes it more flexible to choose the partitions for grouping pvalues.The hierarchical structure optimizes the innerlevel information and transfers it to the outerlevel statistics. Similar structure has been used in ARTP, but it loses some statistical power since it has two layers, and removes the largepvalues using the truncation points. Our method rather keep all the pvalues in different groups. Although theoretically it may increase the computational load due to the requirement of three layers of permutation procedure, we propose a singlelayer permutation procedure to reduce the complexity and shows its effectiveness in experiments. Intuitively, the threelayer structure of the statistic could be generalized to fourlayer, by defining different sets of partition sets. However, threelayer structure is good enough in most scenarios, and increasing layer will introduce more complicated parameter sets and computational complexity.
In our experiments, the multiple partitions are defined by five popular sets of thresholds: [0.01, 0.1],[0.001,0.05], [0.01, 0.05], [0.001, 0.01, 0.1],[0.001, 0.01, 0.05]. Note that the thresholds are all very popular cutoffs used in statistical field and these sets are also used in [10]. We suggest to use these partition sets in the applications. In prin76ciple, a large value of permutation time B is preferred in the experiments because it can yield more accurate null distribution and thus obtain more accurate pvalue. However, a very large B results in extensive computational load. Thus in our experiments, we use B=1000 in simulation studies and B=10,000 in applications, to balance the tradeoff.
Conclusion
We propose a robust statistical method rPCMP by using multiple partitions of pvalues in this work, to reduce the sensitivity of GCP method. The rPCMP statistic is a threelayer statistic, which takes into consideration the different partitions of the individual pvalues. This threelayer statistic could be empirically estimated by a singlelayer permutation procedure. Type I error rates and statistical power are used to evaluate our rPCMP method. The simulations studies show that our proposed rPCAMP test method perform more powerful than some existing pvalue combination methods, with low type I error rates. Our method is finally applied to a ACTCSeq dataset, to find the related gene functions for chromatin states in mouse tumor cells. The proposed method succeeds in detecting significant gene functions for tumorspecific T cell dysfunction and reprogramming. One future research could be to further adapt the current rPCMP for highly correlated individual genes.
Abbreviations
 ARTP:

Adaptive rank truncated product method
 ATACSeq:

Assay for transposase accessible chromatin using sequence
 FCT:

Fisher’s combination test
 GCP:

Group combined pvalue
 rPCMP:

robust pvalue combination by multiple partitions
 SNPs:

Single nucleotide polymorphisms
 TPM:

Truncated product method
References
 1
WTCC C. Genomewide association study of 14,000 cases of seven common diseases and3,000 shared controls. Nature. 2007; 447(7145):661–78.
 2
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, et al.A genomewide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet. 2007; 39(7):870.
 3
Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA, et al.Gene set enrichment analysis: A knowledgebased approach for interpreting genomewide expression profiles. Proc Natl Acad Sci. 2005; 102(43):15545–50. Accessed 7 Dec 2014.
 4
Fisher RA. Statistical methods for research workers. New Delhi: Kalpaz Publications; 2017.
 5
Zheng G, Wu CO, Kwak M, Jiang W, Joo J, Lima JA. Joint analysis of binary and quantitative traits with data sharing and outcomedependent sampling. Genet Epidemiol. 2012; 36(3):263–73.
 6
Li Q, Hu J, Ding J, Zheng G. Fisher’s method of combining dependent statistics using generalizations of the gamma distribution with applications to genetic pleiotropic associations. Biostatistics. 2014; 15(2):284.
 7
Hess A, Iyer H. Fisher’s combined pvalue for detecting differentially expressed genes using Affymetrix expression arrays. Bmc Genomics. 2007; 8(1):96.
 8
Zaykin DV, Zhivotovsky LA, Westfall PH, Weir BS. Truncated product method for combining Pvalues. Genet Epidemiol. 2002; 22(2):170–185.
 9
Dudbridge F, Koeleman BPC. Rank truncated product of P values, with application to genomewide association scans. Genet Epidemiol. 2003; 25(4):360–6.
 10
Hu X, Zhang W, Zhang S, Ma S, Li Q. Groupcombined Pvalues with applications to genetic association studies. Bioinformatics. 2011; 32(18):btw314.
 11
Yu K1, Li Q, Bergen AW, Pfeiffer RM, Rosenberg PS, Caporaso N, et al.Pathway analysis by adaptive combination of Pvalues. Genet Epidemiol. 2009; 33(8):700.
 12
Taylor J, Tibshirani R. A tail strength measure for assessing the overall univariate significance in a dataset. Biostatistics. 2006; 7(2):167–81.
 13
Jiang B, Zhang X, Zuo Y, Kang G. A powerful truncated tail strength method for testing multiple null hypotheses in one dataset. J Theor Biol. 2011; 277(1):67.
 14
Chen H, Pfeiffer RM, Zhang S. A Powerful Method for Combining  Values in Genomic Studies. Genet Epidemiol. 2013; 37(8):814–9.
 15
Westfall P, Young B. ResamplingBased Multiple Testing: Examples and Methods for PValue Adjustment. New York: Wiley; 1993.
 16
Ge Y, Dudoit S, Speed T. Resamplingbased multiple testing for microarray data analysis. Test. 2003; 12(1):1–44.
 17
Schietinger A, Philip M, Krisnawan VE, Chiu EY, Delrow JJ, Basom RS, et al.TumorSpecific T Cell Dysfunction Is a Dynamic AntigenDriven Differentiation Program Initiated Early during Tumorigenesis. Immunity. 2016; 45(2):389–401.
 18
Philip M, Fairchild L, Sun L, Horste EL, Camara S, Shakiba M, et al.Chromatin states define tumourspecific T cell dysfunction and reprogramming. Nature. 2017; 545(7655):452.
 19
Buenrostro JD, Giresi PG, Zaba LC, Chang HY, Greenleaf WJ. Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNAbinding proteins and nucleosome position. Nat Methods. 2013; 10(12):1213.
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Funding
Publication of this article was sponsored by the NSFC projects 11471256 and 11631012 grant.
Availability of data and materials
The datasets are available from reference [18] and http://baderlab.org/GeneSets. Accessed 20 Mar 2018.
About this supplement
This article has been published as part of BMC Systems Biology Volume 12 Supplement 9, 2018: Proceedings of the 29th International Conference on Genome Informatics (GIW 2018): systems biology. The full contents of the supplement are available online at https://bmcsystbiol.biomedcentral.com/articles/supplements/volume12supplement9.
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MC conducted the experiments. LL designed the model and the experiments, and wrote the manuscript. Both authors revised and approved the manuscript.
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Correspondence to Limin Li.
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Cai, M., Li, L. rPCMP: robust pvalue combination by multiple partitions with applications to ATACseq data. BMC Syst Biol 12, 141 (2018) doi:10.1186/s129180180661z
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Keywords
 group pvalue
 multiple partitions
 ATACseq