Abstract
Background
Gene expression is governed by complex networks, and differences in expression patterns between distinct biological conditions may therefore be complex and multivariate in nature. Yet, current statistical methods for detecting differential expression merely consider the univariate difference in expression level of each gene in isolation, thus potentially neglecting many genes of biological importance.
Results
We have developed a novel algorithm for detecting multivariate expression patterns, named Recursive Independence Test (RIT). This algorithm generalizes differential expression testing to more complex expression patterns, while still including genes found by the univariate approach. We prove that RIT is consistent and controls error rates for small sample sizes. Simulation studies confirm that RIT offers more power than univariate differential expression analysis when multivariate effects are present. We apply RIT to gene expression data sets from diabetes and cancer studies, revealing several putative disease genes that were not detected by univariate differential expression analysis.
Conclusion
The proposed RIT algorithm increases the power of gene expression analysis by considering multivariate effects while retaining error rate control, and may be useful when conventional differential expression tests yield few findings.
Background
The problem of detecting a change in expression between two biological states, such as healthy vs. diseased, is central to microarray data analysis. There are two main approaches to this problem: statistical difference tests [1] or feature selection by machine learning techniques [2]. The former alternative provides a solid statistical foundation and allows proper control of false positive rates, but is limited to detecting differences in the expression level of single genes. We herein refer to this as univariate differential expression (UDE). The machine learning techniques on the other hand can potentially discover more complex, multivariate effects, herein referred to as multivariate differential expression (MDE). Figure 1 provides some examples illustrating the distinction between UDE and MDE. However, machine learning techniques usually aim to discover small, predictive gene sets and do not control error rates. Consequently, the gene lists obtained are often unreliable [3,4]. Thus, there is a need for novel methods that combine the best of the two worlds – allowing detection of MDE patterns within a sound statistical framework.
Figure 1. Distribution example. Example twogene distributions with multivariate effects. Each square/cross denotes a sample from one of the classes. Black dashed/gray solid lines denote the corresponding classconditional marginal distributions. A: A PCWT distribution where the gene X_{2 }is UDE (since its classconditional means differ) while X_{1 }is not. B: A PCWT distribution where neither gene is UDE (and hence cannot be detected by standard differential expression tests). C: A nonPCWT distribution. In all cases, both genes are MDE.
Existing solutions to this problem center around the idea of performing statistical tests on gene sets rather than on individual genes. Examples of this include the popular Gene Set Enrichment Analysis [5] method and various multivariate tests [6,7]. This approach permits detection of multivariate effects, but it requires the user to choose the gene sets involved in advance. The latter simplifies the problem considerably, but consequently only permits detection of previously known functional groups such as KEGG pathways [8] or GeneOntology categories [9].
Earlier, Szabo et al. [10] proposed to find novel gene sets by maximizing a test statistic D using subset search. Unfortunately, since exhaustive subset search is intractable for highdimensional data, Szabo et al. are forced to resort to heuristics, considering only gene sets of some a priori fixed size and using randomized search methods. Xiao et al. [11] developed this procedure further and used a permutation test to ensure that D is significantly larger than what would be expected by random. In this way the error rate over gene sets can be controlled, at least approximately. Dettling et al. [12] proposed a different approach for finding gene sets, but only considered sets of size 2 and restricted attention to certain types of bivariate normal distributions.
In our view, a limitation with all of the above methods is that the error rates necessarily concern gene sets, not individual genes. Since a gene set may be significant even when containing only a single true positive gene [10], the false positive rate over individual genes may be much higher than the false positive rate over gene sets. For example, if a single, true gene set containing 10 genes is selected, then the false positive rate over gene sets is zero, while the false positive rate over the genes involved may be as high as 90%. This is appropriate if the investigator is indeed primarily interested in gene sets; but if the primary interest is individual genes, then these methods may be misleading.
In this paper we focus on finding individual MDE genes, not gene sets. We present a principled, generally applicable method which can be seen as a direct generalization of univariate differential expression to the multivariate case. We prove that our procedure is consistent (i.e., given enough samples, it discovers exactly the true MDE genes) for a realistic class of data distributions. Further, we show that our method produces correct pvalues for small samples, and thus controls error rates while offering more power than univariate differential expression testing. Finally, we apply our method to two microarray data sets and conduct a literature validation of the gene lists generated, revealing many potentially important genes that were not detected by the UDE tests.
Theoretical background
Throughout, we assume that samples (arrays) x^{(1)},... x^{(l) }are independent observations of an ndimensional random vector X = (X_{1},..., X_{n}), with classconditional density f(xy), where y ∈ {1, +1} is a class variable denoting the biological condition. For simplicity we here restrict ourselves to the twoclass case, although the theory and methods presented can easily be extended to multiple classes or even continuous Y. For microarray data, we typically have n ≫ l.
We say that a gene X_{i }is univariate differentially expressed (UDE) if the mean expression level for the two conditions differ. Thus we define the set of UDE genes
In figure 1A, this holds for gene X_{2 }but not for gene X_{1}; in figures 1B,C neither gene is UDE. In higher dimensions, similar situations may render a large fraction of the genes MDE yet not UDE. A more general definition is the following: we say that a gene X_{i }is multivariate differentially expressed (MDE) if there exists a gene set S ⊂ {X_{1},... X_{n}} such that X_{i }is conditionally dependent on Y given S. Thus the set of MDE genes is defined formally as
where denotes conditional dependence. This definition recognizes all genes in figures 1A,B,C as MDE. It was initially proposed by Kohavi and John [13]. Clearly, the criterion (1) implies criterion (2), so we have U ⊆ M. Therefore MDE is a generalization of UDE. Genes which are MDE but not UDE cannot be detected by univariate differential expression tests, as shown in figure 1. The goal of this paper is to estimate the set M from expression data.
The set M is typically larger than the set of genes optimal for predicting Y, because some genes in M may be "redundant" – their predictive information can be obtained from other genes, and hence they can safely be excluded from the predictor [13]. Therefore, machine learning techniques that attempt to optimize a predictor (such as the Recursive Feature Elimination [14] used herein) tend to select only a subset of M. Hence, these methods are generally not suitable for our purpose.
Unfortunately, for arbitrary data distributions, determining whether equation (2) holds for a given gene X_{i }requires exhaustive subset search, which is known to be intractable for highdimensional data. However, for a large class of data distributions we herein refer to as the PCWT class (short for Positive/Composition/Weak Transitivity; see Additional file 1 for a rigorous definition), we will prove that the problem is tractable. We will then show that this PCWT class is sufficiently general to be used as a model for biological data, and in particular microarray data.
Additional File 1. Supplementary information. This supplement contains details on the PCWT class, proofs for theorems and an additional simulation study.
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Results
The RIT algorithm
We developed a recursive algorithm named Recursive Independence Test (RIT) based on pairwise tests for marginal independencies. The algorithm pseudocode is given in figure 2A. In the first round, RIT tests for the marginal independencies X_{i }⊥ Y  ∅ for each gene X_{i }and obtains a gene set S of significant findings. Next, for each X_{i }∈ S we recursively call RIT to test for the marginal independencies X_{i }⊥ X_{j } ∅ against each gene X_{j }∉ S, and add the significant findings to S. We continue in this fashion until no more dependencies are found.
Figure 2. The RIT Algorithm. A: Algorithm pseudocode. B: Algorithm example. Edges (solid lines) denote marginal dependencies between genes X_{i }(circles) and the class label variable Y (square). Gene sets found in each round of RIT are denoted S_{1},..., S_{4}. The final output of the algorithm is the union of these.
An illustrating example of an RIT run is given in figure 2B. Here, the MDE genes are M = {X_{1},..., X_{11}}, the UDE genes are U = {X_{1},..., X_{4}}, and the remaining genes are unrelated to Y. In the first round of RIT we obtain the set S_{1}. In this case S_{1 }differs from U, which of course may happen for small sample sizes since the statistical tests used have limited power. In the next recursion, RIT tests the genes in S_{1 }against X \ S_{1 }= {X_{4},..., X_{20}}; this discovers the set S_{2}, which is dependent on X_{2}. Continuing the recursion, RIT eventually finds two more gene sets S_{3}, S_{4}, after which no more significant genes are found and the algorithm terminates. The final output of RIT is then the estimate = S_{1 }∪ S_{2 }∪ S_{3 }∪ S_{4}. In S_{3 }we obtain a false positive X_{12}, and since X_{4 }∉ S_{1}, we also fail to detect X_{9 }because the required test is never made. Since the RIT algorithm only visits each X_{i }∈ once, it is easy to see that the number of tests made is on the order of n. Thus, for reasonably small , the algorithm scales approximately linearly with the number of genes. This is important not only for computational speed, but also to reduce multiplicity problems (see below). Note also that since the first round of RIT is a univariate differential expression test, the set found by RIT always includes the genes found by UDE testing. Hence, RIT always has at least as much statistical power as a UDE test.
Typically, one needs to use two different independence tests with RIT, since the class variable Y is different from the genes X_{i}. For simplicity, in our simulations (below) we have used the wellknown Student's ttest for X_{i }⊥ Y  ∅ and Fisher's ztransformation for testing X_{i }⊥ X_{j } ∅. The ttest is optimal (unbiased most powerful) for gaussian marginal distributions [15], but on the other hand is correct only for these distributions, which constitute a subset of larger PCWT distribution class (see Additional file 1). Fisher's z is consistent regardless of distribution. While the gaussian assumption is frequently made in gene expression analysis, for example in gene network inference [16], we emphasize that RIT is itself not restricted to this class. As an example, we applied RIT to 100 samples drawn from the nonlinear distribution in figure 1B using the distributionfree KolmogorovSmirnov test [17] for X_{i }⊥ Y and the Spearman Rank Test [17] for X_{i }⊥ X_{j}, both at the 5% level. This produced the correct result (S_{1 }= {X_{2}}, S_{2 }= {X_{1}}) in 99 runs out of 100 (the single error made was a false positive X_{2 }in S_{1}). Applying same tests to the distribution in figure 1C gave no significant findings, since this distribution is not in the PCWT class and therefore not detectable by RIT.
Consistency of the RIT algorithm
Remarkably, the comparatively simple RIT algorithm can be shown to be consistent for any PCWT distribution; that is, as sample size increases, the RIT output converges to the set of MDE genes M. To prove this, note that RIT constructs a path from Y to each gene X_{k }in the graph whose edges (i, j) correspond to the pairwise marginal dependencies X_{i }X_{j } ∅ (i.e., the graph in figure 2B). The following theorem states that for PCWT distributions, the set of genes reachable through such paths coincides with the set M defined in equation (2).
Theorem 1 For any PCWT data distribution, the set of MDE genes M is identical to the set of genes = {X_{k }∈ X} for which there exists a sequence = {Z_{1},..., Z_{m}} ⊆ X between Z_{1 }= Y and Z_{m }= X_{k }such that Z_{i }Z_{i+1 } ∅, i = 1,..., m  1.
The full proof of this theorem is given in Additional file 1. If the data distribution is not PCWT, the theorem may not hold; figure 1C shows a typical counterexample. Assuming that the independence tests used are consistent, consistency of the RIT algorithm immediately follows from the above. This result is a good argument in favor of RIT, since consistency is a widely accepted necessary condition for a sound statistical procedure [15]. To our knowledge, no other algorithm for detecting MDE genes has been proven to be consistent.
Biological relevance of the PCWT class
Next, we will show that the PCWT class is a reasonable model for gene expression data (or, more generally, for any measurements of biological systems). Since cellular systems are believed to be well described by complex networks [18], it is reasonable to assume that the distribution of all variables X' comprising a cellular network (transcripts, proteins, metabolites, etc.) can be modelled as a Bayesian network [19]. The following theorem, given by [20], asserts that the PCWT class contains all data distributions associated with such networks.
Theorem 2 Any strictly positive distribution faithful to a Bayesian network is PCWT.
However, we typically cannot measure all variables X', but merely a subset X; for example, with microarrays we can perhaps measure most transcripts but no proteins or metabolites. Unfortunately, this means that in many cases X cannot be modelled by a Bayesian network [21]. Nevertheless, the next theorem asserts that X is still PCWT.
Theorem 3 Let X' be a random vector with a PCWT distribution and let S, T be any two disjoint subsets of the components of X'. Then with probability 1, the distribution of X = (X' \ {S, T}  T = t) is also PCWT.
The proof is found in theorems 5 and 6 of [22]. Theorem 3 states that for PCWT distributions, we may fix some variables T to constant values t and ignore other variables S, and the remaining variables will still form a PCWT distribution. Thus, given that the distribution of all variables X' comprising the cellular network are PCWT, then any measurements X we make will also have a PCWT distribution, even though we fail to measure many variables of the system and perhaps fix others to constant values by experimental design. We therefore conclude that PCWT is a realistic distribution class for biological data.
Multiplicity and FDR control
Consistency is an asymptotic result however, and is still far from satisfactory for the small sample sizes typical for microarray data. Due to the large amounts of tests made, it is necessary to properly adjust for multiplicity, or else many findings are likely to be false positives. This issue has been thoroughly investigated for univariate tests [1], but our situation is more complicated since RIT performs multiple iterations of testing, and also chooses which tests to make in each iteration depending on the outcome of the previous one.
To ensure multiplicity control, we employ an induction argument. Fix an α ∈ [0, 1]. Assume as the induction hypothesis that in the first foreach loop of the algorithm (figure 2A) we have tested the null hypotheses = X_{i }⊥ Y  ∅ for each X_{i }and obtained pvalues p_{i }for each X_{i}. We then sort these to obtain the order statistics p_{(1) }≤ p_{(2) }≤ ... p_{(n)}, and apply a correction procedure to choose a gene set S (a "top list") with corrected pvalues _{i }satisfying
This requirement is slightly weaker than FWER control, and is satisfied by the FDRcontrolling procedure of Benjamini and Hochberg [23] (see Additional file 1 for a proof), which we employ in this paper. Other FDRcontrolling procedures could probably also be used for obtaining S, but we have not attempted to prove (3) in the general case.
Now consider the recursive calls RIT(X \ S, X_{i}). For each X_{i }∈ S, this will test the null hypotheses = X_{i }⊥ X_{j } ∅ for every X_{j }∉ S, producing the pvalues p_{ij}. We now combine the previously obtained _{i }with these p_{ij }to obtain a single pvalue p_{j }for each X_{j }∉ S. To accomplish this, note that by theorem 1 X_{j }∉ M is possible at this point only if, for every X_{i }∈ S, either or holds true. Hence, the null hypothesis for X_{j }is
This situation is known in statistics as intersectionunion testing [24,25]. By the intersectionunion method, a level α test for is
and the corresponding pvalue p_{j }is computed as
The factor S derives from a Bonferroni correction for the outer intersection in (4). This completes the induction step; as the induction hypothesis is easily satisfied in the first round of testing, it follows by induction that with these corrections, RIT always yields pvalues. Finally, the BenjaminiHochberg procedure may be applied again to control the false discovery rate. Alternatively, more stringent measures such as familywise error rate control [26] may be used, if desired. Formal proofs of the correctness of each of the above steps can be found in Additional file 1. A detailed pseudocode of RIT implementing each step is given in Additional file 3.
Simulated data
To illustrate the above result and also to assess the statistical power of RIT as a function of the sample size, we conducted a simulation study. To this end, we designed a distribution with multivariate differential expression, chosen so that 10% of the genes were MDE, but only half of these (5%) were UDE and thus detectable a univariate test (see methods section for details). We compared the performance of RIT against a typical univariate test, namely Student's ttest [15] with FDR correction [23], and also against the popular Recursive Feature Elimination (RFE) feature selection method [14].
Figure 3 summarizes the results of this experiment. We find that RIT does indeed control the FDR at the nominal level (α = 0.05), in the same way as the univariate test. The power of the univarate test converges to 0.5 as expected (since only half of the MDE genes were UDE), while the RIT converges to 1.0, in agreement with our theoretical results. Thus, when multivariate effects are present, RIT affords more power than the univariate test at the same FDR level. In contrast, the RFE method clearly does not control the FDR, choosing many genes unrelated to Y. RFE also displays low power, most likely because it considers some MDE genes to be "redundant" for prediction and consequently ignores these. Similar behavior is to be expected from other feature selection methods, as explained above. A second simulation study using a different distribution was also performed, with similar results (see Additional file 2). We conclude that it is feasible to apply the RIT algorithm to smallsample data while controlling the FDR at the desired level. Exact sample size requirements cannot be inferred from figure 3 however, as this depends on the data distribution, in particular the fraction of MDE genes and the amount of noise.
Additional File 2. Supplementary figure 1. Describes the second simulation study.
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Additional File 3. Supplementary figure 2. Contains the pseudocode for the RIT algorithm with pvalue corrections. Software availability. The RIT algorithm is available as a Mathematica notebook upon request.
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Figure 3. Simulation results. Simulation results for the RIT algorithm, differential expression using the ttest, and RFE. Left, statistical power (1 – false negative rate) as a function of sample size. Right, false discovery rate (FDR) as a function of sample size. Grey arrow marks the nominal FDR = 0.05.
Microarray data
We next tested the RIT algorithm on two publicly available microarray data sets (see methods section). The diabetes data contrasts pancreas islets expression from normal vs. type 2 diabetic patients [27]. The original study identified 370 genes as UDE, but this did not account for multiplicity. The qvalue method declared only the top three genes of the original study to be significant: Arnt, Cdc14a, and Ddx3y. The RIT algorithm identified an additional 21 transcripts as MDE, of which 5 were unknown EST:s and 16 were known genes according to the NCBI Gene database [28]. We would like to stress that RIT is an hypothesesgenerating method, and that the discovered MDE genes may or may not be of functionally related to the target variable. Nevertheless, we conducted a literature validation of the 16 known genes (table 1) to search for possible biologically important findings. Five of these (31%) were previously associated with diabetes. Among the remaining 11 novel genes, several give rise to interesting hypotheses: for example, Dopey1 was recently shown to be active in the vesicle traffic system, the mechanism that delivers insulin receptors to the cell surface. Four genes encoded transcription factors, as do the majority of previously discovered diabetesassociated genes [27]. The Usp9y gene discovered by RIT is associated with male infertility and Sertoli cellonly syndrome. Interestingly, so is the UDE Ddx3Y gene. This is unlikely to be a coincidence as only 6 human genes were annotated with this function in NCBI Gene. This is an example of general tendency we have observed in our experiments, that additional MDE genes discovered by RIT often are functionally related to the UDE genes, which is hardly surprising given that RIT relies on pairwise independence test. The chloride channels Clca2 and Clcn1 are also highly interesting findings, as ion channels in pancreas islets has been shown to regulate insulin secretion [29]. The diabetesassociated potassium ion channel Kcng1 was also discovered by RIT, strengthening this hypothesis.
Table 1. Diabetesrelated genes. Genes with multivariate expression patterns discovered by the RIT algorithm for the diabetes data.
The breast cancer data contrasts goodprognosis vs. poorprognosis patients [30]. This set had large amounts of pairwise correlations among genes, resulting in a highly connected dependence graph. To limit the number of findings in this case, we required significant correlations to exceed a threshold 0.85 to be considered by RIT (see discussion). The original study identified a set of 70 cancerrelated genes. In addition to these, the RIT algorithm identified 43 MDE genes. Literature validation revealed that 23 of these (53%) had a previously known function in cancer development, whereof 6 (14%) were specifically implicated in breast cancer (table 2). An additional 10 transcripts (23%) were cell cyclerelated and may also be considered as potential cancer proliferation genes. Our literature validation thus confirmed 39 (77%) of the genes reported by RIT to be cancerrelated. The higher percentage in this case as compared to the diabetes data may reflect the fact that more genes are known for cancer than for diabetes. To assessed the amount of cancer annotations among the 5,000 genes considered, we examined an additional 43 genes chosen at random. Indeed, we found that about 25% of all genes had some cancer or cell cyclerelated annotation. Nevertheless, the above fraction of 77% validated genes is highly significant with a Binomial tail pvalue < 10^{20}.
Table 2. Breast cancerrelated genes. Genes with multivariate expression patterns discovered by the RIT algorithm for the breast cancer data.
Encouraged by the above result, we set out to investigate the remaining 10 genes that were not previously associated with cancer. We found three histone proteins, which may be related to chromatin remodelling. One novel gene Gpr116 was recently identified as a Gprotein with a potential role in immune response. The novel gene Prr11 had predicted binding sites for the transcription factor E2F, which in turn is known to be crucial in the control of tumorigenesis. Ube2s is an essential component of the ubiquitinprotein conjugation system, which is implicated in various cancer forms. This gene is also functionally related to the known cancer gene Ube2c, which also was discovered by RIT. Also interesting were the novel proteins Depdc1 and Depdc1b, both containing RhoGAP domains. This may implicate them in the regulation of various Rho GTPases, which are currently being investigated as cancertherapy targets [31].
Discussion
At a first glance, RIT might seem similar to existing algorithms for "local" network inference around "seed genes" [32,33]. However, network inference is a much harder problem than detecting MDE, and typically requires testing for conditional independence (while RIT requires only marginal independence tests). Consequently, these algorithms require substantially larger samples and stronger distribution assumptions, and their timecomplexity is exponential with respect to the number of genes found [33].
RIT is less useful for data with large and strongly correlated transcriptional changes, such as the breast cancer data set considered herein. For cancer data, even the (smaller) fraction of UDE genes has been estimated to be on the order of 50% of all genes [34], and the set of MDE genes is presumably much larger. Thus, the concept of MDE is simply not very useful in this case, since most genes turn out to be MDE. Thus, a principled approach for prioritizing among all these genes is urgently needed. For the cancer data, we let RIT prioritize the findings by considering stronger correlations to be more important. This seems reasonable, and we were able to confirm the end results in this case against the literature. However, this problem is ultimately unsolvable by statistical methods, and must instead be addressed by integrating other kinds of information. A possible step towards a principled solution building upon the present work would be to combine the independence tests used here with other data sources and prior beliefs (perhaps in the form of Bayesian probabilities) to guide the RIT algorithm towards more "interesting" genes.
It is important to realize that RIT does not perform feature selection in the usual machine learningsense: feature selection aims to find the set of features (genes) optimal for constructing an accurate predictor of the target variable, while RIT aims to find the MDE genes, which need not be optimal for prediction.
These are two different problems, and they should be treated separately.
In this study we have limited ourselves to twoclass data. However, it is straightforward to extend the RIT algorithm to find multivariate expression patterns with other types of target variables, such as multiple classes data or continuous target variables such as survival times. To accomplish this, only the independence tests used need to be replaced. This "modularity" is a useful property of RIT: to handle different situations, it is sufficient to "plug in" different independence tests. For example, a continuous target variable could be handled by using the Fisher ztransformation also for testing X_{j }⊥ Y. More complex, nonlinear independence relations may be handled using nonparametric tests such as the KolmogorovSmirnov test [17] or kernelbased tests [35]. However, a basic limitation of the RIT algorithm is that at least one gene must be UDE for any MDE genes to be found. This is an inherent property of the PCWT class.
Dynamic (timeseries) data could also be considered, although some additional assumptions may be necessary to ensure PCWT distributions in this case. For example, assuming a Markov condition, timeseries data can be modelled using Dynamic Bayesian Networks (DBNs) [19]. The DBN methodology essentially transforms a dynamic model over n nodes into an ordinary BN over 2n nodes. Thus, DBNs also result in PCWT distributions as described herein (albeit of twice the dimensionality) and RIT is therefore applicable to detecting multivariate changes in dynamic as well as in static data.
Conclusion
The RIT algorithm is a principled, general approach that increases the power of smallsample, genomewide expression studies by considering not only univariate differential expression but also multivariate effects. In contrast to previous approaches which focus on testing gene sets [57,10,11], RIT gives a pvalue for each gene and provides control over false positive findings in terms of individual genes. RIT may be very useful in situations where little univariate differential expression is observed, as exemplified by the diabetes data experiment.
Methods
Simulation study
In our simulations, we used a multivariate gaussian distribution with n = 1, 000 genes and M = 100 MDE genes, of which U = 50 were differentially expressed. We first designed a 4dimensional gaussian distribution with a classdependent mean vector μ_{y }= 2y·(0, 0, 1, 1) and covariance matrix
equal for both classes. We then constructed the full distribution for the 100 MDE genes using 25 of these 4blocks. The remaining features had the same covariance matrix but had mean μ = (0, 0, 0, 0). We varied the sample size as 10, 20, 30,..., 100.
The Recursive Feature Elimination (RFE) procedure was implemented as described [14], eliminating 20% of the genes in each iteration. We used the radiusmargin bound proposed by [36] as a goodness measure for choosing the optimal gene set.
Microarray data sets
The diabetes data set is from the study by Gunton et al. [27] and is publicly available at the Diabetes Genome Anatomy Project [37]. This data set contrasts human pancreas islets expression from normal (n = 7) vs. type 2 diabetic (n = 5) patients. The original data comprises 44,928 probesets from the Affymetrix U133A and B chips. We used only the A chip in our experiments, since we needed to evaluate our results against literature and the A chip contains better annotated sequences. Moreover, since initial analysis using the full A chip resulted in no significant findings, we reduced multiplicity by prefiltering genes by variance, keeping only the 5,000 most variable genes.
The breast cancer data set consist of 78 samples from patients divided into one "good prognosis" group (n = 44) and one a "poor prognosis" group (n = 34) based on the time until relapse [30]. The data set is freely available from Rosetta Inpharmatics [38]. The arrays used contains approx. 25,000 transcripts, out of which 4,918 were selected using the same quality filter as in the original publication.
Authors' contributions
RN devised the multiple comparison procedure, performed the simulation study and the application to the microarray data sets, performed most of the literature validation, and wrote most of the manuscript. JMP devised the basic idea for the RIT algorithm and the wrote the proof of theorem 1. JB assisted with the literature validation. JT participated in study design and cowrote the manuscript.
Acknowledgements
This work was supported by grants from the Ph.D. Programme in Medical Bioinformatics, the Swedish Research Council (VR62120054202), Clinical Gene Networks AB and Linköping University.
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