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Multi-level block permutation

Anderson M. Winkler, Matthew A. Webster, Diego Vidaurre and 2 more

NeuroImage · 2015 · CC BY

doi:10.1016/j.neuroimage.2015.05.092

Abstract

Under weak and reasonable assumptions, mainly that data are exchangeable under the null hypothesis, permutation tests can provide exact control of false positives and allow the use of various non-standard statistics. There are, however, various common examples in which global exchangeability can be violated, including paired tests, tests that involve repeated measurements, tests in which subjects are relatives (members of pedigrees) - any dataset with known dependence among observations. In these cases, some permutations, if performed, would create data that would not possess the original dependence structure, and thus, should not be used to construct the reference (null) distribution. To allow permutation inference in such cases, we test the null hypothesis using only a subset of all otherwise possible permutations, i.e., using only the rearrangements of the data that respect exchangeability, thus retaining the original joint distribution unaltered. In a previous study, we defined exchangeability for blocks of data, as opposed to each datum individually, then allowing permutations to happen within block, or the blocks as a whole to be permuted. Here we extend that notion to allow blocks to be nested, in a hierarchical, multi-level definition. We do not explicitly model the degree of dependence between observations, only the lack of independence; the dependence is implicitly accounted for by the hierarchy and by the permutation scheme. The strategy is compatible with heteroscedasticity and variance groups, and can be used with permutations, sign flippings, or both combined. We evaluate the method for various dependence structures, apply it to real data from the Human Connectome Project (HCP) as an example application, show that false positives can be avoided in such cases, and provide a software implementation of the proposed approach.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 18, 2026. Paragraph numbers are ours, so an answer can point at one.

Introduction

In the context of hypothesis testing using the general linear model (glm), permutation tests can provide exact or approximately exact control of false positives, and allow the use of various non-standard statistics, all under weak and reasonable assumptions, mainly that the data are exchangeable under the null hypothesis, that is, that the joint distribution of the error terms remains unaltered after permutation. Permutation tests that compare, for instance, groups of subjects, are of great value for neuroimaging, and in, extensions were presented to more broadly allow tests in the form of a glm, and also to account for certain types of well structured non-independence between observations, which ordinarily would preclude the use of permutation methods. This was accomplished by redefining the basic exchangeable unit from each individual datum to blocks of data, i.e., rather than asserting exchangeability across all observations of a given experiment, blocks of exchangeable units are defined; these exchangeability blocks (ebs) can be rearranged as a whole (whole-block exchangeability), or the observations within block can be shuffled among themselves (within-block exchangeability), using either permutations, sign flippings, or permutations combined with sign flippings.

In the same work, the G-statistic, a generalisation over various commonly used statistics, including the F-statistic, was proposed. G is robust to known heteroscedasticity (i.e., the situation in which the variances are known to be not equal across all observations, which can be then classified into variance groups) and can be used with the glm, ensuring that pivotality1 is preserved, a crucial requisite for exact control over familywise error rate (fwer) using the distribution of the most extreme statistic, as needed in many neuroimaging studies. Indeed, the use of ebs allows for variances to be heterogeneous, provided that the groups of observations sharing the same variance (i.e., variance groups, vgs) are compatible with the ebs; specifically, for within-block exchangeability the vgs must coincide with the blocks, and for whole-block exchangeability they must include one or more observations from each block in a consistent order.

This arrangement, using a statistic that is robust to heteroscedasticity, the use of variance groups, and the imposition of restrictions on exchangeability through the use of ebs, allows inference on various designs that, otherwise, would be much more difficult to do non-parametrically. These designs include paired tests, longitudinal designs, and other common tests that involve repeated measurements. However, certain study designs, despite exhibiting well-structured dependence between observations, still cannot be accommodated in the above framework. This occurs when the overall covariance structure is known, but its exact magnitude is not. An example occurs when multiple measurements per subject are performed in more than one session, with more than one measurement per session: the measurements within session may be exchangeable, but not across sessions. Another example is for studies using siblings, such as designs using discordant sib-pairs (in which only one sibling is affected by a given disorder), or using twins: permutations that disrupt the constitution of any sibship cannot be performed, as this would violate exchangeability.

Studies such as these are relatively common, notably those that involve siblings. However, whereas in classical twin designs the central objective is to quantify the fraction of the variation in a measurement (trait) that can be explained by the familial relationship between subjects after potential confounds have been taken into account, a quantity known as heritability, here the concern is with a general linear model, and the objective is to test the influence of explanatory variables on the observed data. In other words, the interest lies on the relationship between the covariates and the main trait, while the non-independence between observations, which is a feature of interest in a heritability study, is here a form of nuisance that imposes restrictions on exchangeability for permutation inference for the glm.

Rather than inadvertently breaking these restrictions, here we propose to test the null hypothesis using a subset of all otherwise possible permutations, only allowing the rearrangements that respect exchangeability, thus retaining original joint distribution unaltered.2 As in our previous work, we treat observations or entire blocks of data as weakly exchangeable, but here we further extend the definition of ebs to allow more complex designs to be addressed. This is accomplished through the use of multi-level exchangeability blocks, in which levels consist of nested blocks; for each such block the state of within- or whole-block exchangeability can be specified. The blocks are defined hierarchically, based on information about the dependence within data, but not requiring the modelling of the actual dependency. Even though the possibility of using nested blocks was anticipated in (“Whole-block and within-block can be mixed with each other in various levels of increasing complexity”, page 386), nothing further was studied or presented at the time. Here we provide a comprehensive description of the approach, investigate its performance, its power, and present an applied example using the data structure of the ongoing Human Connectome Project (hcp). In the Appendix A, we present an implementation strategy.

Terminology

When contrasting the method described in this article with simple data rearrangement, various terms could be adopted: single-level vs. multi-level block shuffling, emphasising the levels of relationship between observations; unrestricted vs. restricted, emphasising the imposition of restrictions on how the data are allowed to be rearranged at each shuffling; free vs. tree shuffling, emphasising the tree-like structure of the relationships between observations that allow shuffling. All these terms have equivalent meaning in the context of this article, and are used interchangeably throughout. The generic terms shuffling and rearrangement are used when the distinction between permutations, sign flippings or permutations with sign flippings is not relevant.

Notation

We consider a glm that can be expressed as Y = Mψ + ϵ, where Y is the N × 1 vector of observed data, M is the full-rank N × r design matrix that includes explanatory variables (i.e., effects of interest and possibly nuisance effects), ψ is the r × 1 vector of r regression coefficients, and ϵ is the N × 1 vector of random errors. Estimates for the ψ can be computed by ordinary least squares, i.e.,, where the superscript (+) denotes a pseudo-inverse. One generally wants to test the null hypothesis that a given combination (contrast) of the elements in ψ equals to zero, that is, 0: C′ψ = 0, where C is a r × s full-rank matrix of s contrasts, 1 ≤ s ≤ r. The commonly used F statistic can be computed as usual and used to test the null hypothesis. When s = 1, the Student's t statistic can be computed as. A p-value for the statistic is calculated by means of shuffling the data, the model, the residuals, or variants of these (, Table 2). In any of these cases, to allow rearrangements of the data, some assumptions need to be made: either of exchangeable errors (EE) or of independent and symmetric errors (ISE). The first allows permutations, the second sign flippings; if both are available for a given model, permutations and sign flippings can be performed together. These rearrangements are represented by permutation and/or sign flipping matrices P, and the set of all such matrices allowed for a given design is denoted as.

At its simplest, the ebs for within- or whole-block exchangeability can be identified or represented by a set of indices {1,2…,B}, one for each of the B blocks. A vector of size N × 1, can be used to indicate to which eb each observation from Y belongs (Fig. 1, left); an extra flag is passed to the shuffling algorithm (such as the randomise algorithm) to indicate whether the rearrangements of the data should happen as within- or as whole-block. While this notation probably covers the majority of the most common study designs, it allows only within- or whole-block, but not both simultaneously; in other words, if in a study the observations can be permuted within block, and the blocks as a whole can also be permuted, such notation does not convey all possibilities for reorganising the data while preserving their joint distribution unaltered, and algorithms would perform fewer shufflings than those that are effectively allowed.

This can be addressed by extending the notation from a single column to a multi-column array, allowing nested ebs to be defined, such that blocks can contain sub-blocks, in a hierarchical fashion, and where each column represents a level; we use the leftward columns to indicate higher, and rightward to indicate lower levels. More columns alone, however, are not sufficient, because at each level, shufflings of observations or of sub-blocks can be allowed within-block, or the blocks at that level can be shuffled as a whole. Hence to discriminate between one type or the other, we use negative indices to indicate that the exchangeable units at the level immediately below should not be permuted, and positive indices indicate that shuffling of these units is allowed (Fig. 1, right). The exchangeable units can be sub-blocks, which can contain yet other sub-blocks, or observations if the next level immediately below is the last.

These two notations, i.e., using single- or multi-column indices, do not represent mathematical entities, and are not meant to be used for algebraic manipulation; rather, these notations are shorthand methods to represent structured relationships between observations. The covariance structure prevents unrestricted shuffling from being considered, but it often permits shufflings to happen in a certain orderly manner that preserves the joint distribution of the data. These notations are to be used by the algorithm that performs the test to construct the permutation and/or sign flipping matrices, which then can be used to effectively disarrange the model to construct the distribution of the statistic under the null hypothesis.

Visual representation

The notation using multiple columns encapsulates all the information necessary not only for the rearrangements to be constructed, but also to depict the relationships between the observations in a tree-like diagram, highlighting their hierarchy, as shown in Fig. 2. Branches can only be shuffled with each other if their size and internal covariance structure are perfectly identical; this information is contained in the signs and indices used to represent each block: positive indices (shown in blue) allow them to be permuted; negative (in red) prevents permutation and keeps the branches in their fixed positions. The permutation of branches at lower levels (when these exist) is controlled by the nodes at these lower levels, independently from those at higher levels or within the same level.

Using the tree diagram, it becomes clear that the terms “within-block” and “whole-block”, that have been used so far to describe exchangeability and permutation strategies, become no longer necessary, as either the branches can be shuffled, or they cannot. It is also helpful in emphasising that more complicated designs can be considered using multi-level blocks, in which even the distinction between within- and whole-block is softened, as each level in the multi-column notation is not restricted to contain purely positive or negative indices restricting (or not) the shuffling of their constituent sub-blocks (branches). These can be present alongside each other if immediately below a level in which shuffling is not allowed, such that some branches may be allowed to be shuffled, whereas others are not. It may also be the case that some levels need to be included in the notation only so that the number of levels remains the same across all branches of the tree, from the top node to the most distal (leaves), without affecting the construction of, but ensuring that the notation can be stored, without gaps, in a two-dimensional array; in the visual representation these are shown as small, sign-less, black nodes. Fig. 3 (left and centre) exemplifies these cases. Although the multi-column notation and the corresponding tree can become very complex, the simple, unrestricted exchangeability can also be accommodated, as shown in Fig. 3 (right).

Variance groups and the G-statistic

When the variances can be assumed to be the same throughout the sample, the classical F and the Student's t statistics can be used; these statistics have sampling distributions that do not depend on any unknown population parameters, but solely on the degrees of freedom, i.e., these are pivotal statistics. However, if homoscedasticity cannot be assumed, although F and t can still be used with permutation tests in general, they cannot be used to correct for multiple testing using the distribution of the most extreme statistic. The reason is that under heteroscedasticity, these statistics cease to be pivotal, and follow instead distributions that depend on the heterogeneous variances for the different groups of observations, causing them to be no longer adequate for fwer correction. Instead, a statistic that is robust to heteroscedasticity is necessary.

The G-statistic was proposed to address this concern; this statistic is a generalisation of various other well established statistics, including F and t, as well as the v-statistic used for the classical Behrens–Fisher problem. The definition of the variance groups used to calculate G is based on knowledge about the data, and such groups need to be constructed together with the definition of the blocks. However, vgs and ebs represent different concepts; although they may coincide for simple designs, they do not need to. The ebs are used to indicate sets of observations that must remain together in every permutation due to having a non-diagonal covariance structure, and are used by the permutation algorithm to rearrange the data many times to build the empirical distribution. The vgs, however, are used to indicate sets of observations that possess the same variance, and are used to estimate the sample variance(s) when computing the statistic. Despite the distinction, any pair of observations that have the possibility of being swapped according to the eb structure must be in the same vg; observations in different variance groups cannot be permuted as that would modify the joint distribution, thus violating exchangeability.

For simple within-block permutation, the most restrictive configuration for the variance groups, that is, the configuration in which fewer observations need to be assumed to share the same variance, is such that each block corresponds to its own vg. For simple whole-block permutation, on the other hand, the first observation from each block, together, constitute a vg, the second observation from each block, together, another vg, and so forth. The minimum set of variance groups for more complicated designs can be derived from the configuration of the exchangeability blocks; examples are shown in Fig. 4. The stringency of this definition lies in that, depending on the configuration of the ebs, each vg can contain only the smallest possible number of observations that can be assumed to have the same variance given the covariance structure imposed by the blocks. Such definition can, however, be relaxed by merging these minimum groups whenever homoscedasticity across more than one vg can be considered, while retaining the ebs unaltered. Whether merger, or any other definition, for the vgs should be sought for a given design may depend on information about the data or on the design itself. For a simple paired t-test, for instance, although each pair could in principle constitute a vg on its own, homogeneous variances can fairly well be assumed, with the benefit of much better variance estimates than would be obtained with groups of two sole observations.

Regardless of which strategy is used to define the variance groups, and irrespective of the indices used to represent each of them, the column vector containing these indices must be invariant with respect to the permutations that are allowed for a given design. In other words, let v be the column vector of length N containing the indices that represent each variance group, such as those in Fig. 4. For any permutation matrix, Pv = v, that is, v is a common eigenvector for all permutation matrices in. Any permutation that breaks this equality must not be used to test the null hypothesis, as this would mix observations that belong to different vgs, thus violating exchangeability. Likewise, a definition of groups that does not meet this criterion must not be used.

Number of permutations

With the multi-level block permutation strategy, the rules to calculate the number of permutations are similar, yet more general than in the case of a single level that could be represented with a single-column notation. The number still depends on the number of repeated rows in the design matrix for methods as Manly and ter Braak or, for methods as Draper–Stoneman and Freedman–Lane, on the number of repeated rows across only the columns that are tested in the contrast after the model has been partitioned into effects of interest and nuisance effects.

Once the tree has been constructed, for the ee assumption, and in the absence of repetitions in the design as described above, the number of permutations can be calculated separately for each node in which shuffling is allowed as B !, with B denoting the number of branches that begin at that node. If however, there are branches with identical structure and containing the repetitions in the design matrix, the number of possible permutations for that node is then B !/∏m = 1MBm !, where M is the number of unique branches beginning at that node, and Bm the number of times each of the M unique branches begins at that node. The number of permutations for nodes that cannot be permuted is simply 1, that is, no permutation. With the number of permutations at each node calculated, the overall number of possible permutations for the whole design (whole tree) is the product of the number of possible permutations for all the nodes.

For ise, the number of sign flippings at the highest node in which shuffling is allowed is 2B, and 1 for all other nodes that lie below (distal) in the hierarchy. For the nodes in which shuffling is not allowed, the number of possible flips is 1, that is, no sign flippings are allowed, but it can still be higher than 1 for the nodes that lie below in the hierarchy. Unlike with permutations, the eventual presence of repeated elements in the design matrix does not affect the number of possible sign flippings. The number of possible sign flippings for the whole design is the product of the number of sign flippings for all the nodes.

When both ee and ise assumptions are valid for a given design, permutations can happen with sign flipping, and the total number of possible rearrangements is just the product of the number of permutations with the number of sign flippings. Regardless of the kind of shuffling strategy adopted, the number of possible rearrangements can be extremely large, even for sample sizes of relatively moderate size. Not all of them need to be performed for the test to be valid and sufficiently exact; a random subset of all possible rearrangements can be sufficient for accurate hypotheses testing.

Power and outliers

The set of all rearrangements that can be performed while respecting the structure of the data is termed the permutation space. The restrictions imposed by the ebs cause this space to be reduced, sometimes considerably, as none of the rearrangements that would violate exchangeability are performed. If the restrictions are such that the permutation space is not a representative, uniform sample from what the space would be without such restrictions, power may be reduced. In the Evaluation method section we assess various configurations for the multi-level ebs and their impact on the ability to detect true effects.

For the same reason, even though most permutation strategies tend to be robust to outliers, the dependence structure and the multi-level blocks may amplify the effect of their presence, with results that may be difficult to predict, either in terms of conservativeness or anticonservativeness. Such problems may be minimised by providing some treatment of these extreme values; some possible remedies include censoring, trimming, replacement for ranks or quantiles, conversion of quantiles to a normal distribution, and robust regression.

Error rates and power

Two dependence structures, named datasets a and b, were simulated to evaluate the permutation strategy. Both use mixtures of levels that can or that cannot be shuffled. For the dataset a, N = 36 observations were simulated, grouped into nine exchangeability blocks of four observations each, and each of these further divided into two blocks of two. Not all levels were allowed to be shuffled freely, and the structure is shown in Fig. 5 (left). For dataset b, N = 27 observations were divided into nine ebs of three observations each; and each of these further divided into two blocks, one with two, and one with one observation, as shown in Fig. 5 (right). Although these may appear somewhat artificial for practical use, we wanted examples that would restrict the number of possible shufflings, to test the multi-level strategy in relatively difficult scenarios. The structure in dataset a precisely emulates a twin study with nine sets of siblings, each comprised of a pair of monozygotic twins and a pair of non-twins (or of dizygotic twins). Dataset b uses a similar scheme, but further restricts the possibilities for shuffling by having just one non-twin in each set of siblings.

Using the same notation as in the Notation section, 500 response variables (data vectors Y) were simulated for each dataset, using the model Y = Mψ + ϵ; each variable might represent, for instance, a voxel or vertex in a brain image. The residuals, ϵ, were simulated following either a Gaussian distribution (with zero mean and unit variance), a Weibull distribution (skewed, with scale parameter 1 and shape parameter 1/3, shifted and scaled so as to have expected zero mean and unit variance), or a Laplace distribution (kurtotic, with zero mean and unit variance).3 In order to introduce dependence between the residuals, for simplicity and without loss of generality to any study in which there is dependence among the data, including repeated measurements, each observation was treated as if from a participant in a twin study design, as described above, and an N × N correlation matrix Ω, was created using the coefficient of kinship, 2ϕij, between subjects i and j, such that Ω = 2Φhϵ2 + I(1 − hϵ2), where Φ is the matrix with the coefficients ϕij, and I is the identity matrix. The benefit of constructing the simulations in this way is that the strength of the dependence structure can vary linearly in the interval 0 to 1 using a single parameter, here denoted as hϵ2, which coincides, in quantitative genetics and under certain assumptions, with the heritability of the measurement after explanatory or nuisance variables have been considered. The coefficient of kinship (2ϕij) is set to 1 for monozygotic twins, 0.5 full siblings that are not monozygotic twins, 0.25 for half siblings, and 0 for unrelated subjects. For these simulations, we used different values for the heritability of the residuals as hϵ2 = {0, 0.4, 0.8}. To introduce the desired correlation structure, Ω was subjected to a Cholesky decomposition such that Ω = L′L, then redefining the residuals as L′ϵ.

The dependent data, Y, were generated by adding the simulated effects, Mψ, to the residuals, ϵ, with ψ = [ψ1 0]′, ψ1 being either 0 or, where α = 0.05 is the significance level of the permutation test to be performed at a later stage, ensuring a calibrated signal strength sufficient to yield an approximate power of 50% with Gaussian errors, irrespective of the sample size. The actual effect was coded in the first regressor only, here denoted m, the second regressor modelling an intercept. This regressor was constructed as a set of random values following a Gaussian distribution with zero mean and unit variance. As in real experiments, such effects of interest may be (as with the residuals) not independent across observations, three different values for the strength of this dependence were simulated, using hm2 = {0, 0.4, 0.8} These values are equivalent to the heritability of m in the context of genetics, yet without loss of generality to studies in which there is dependence between the data that constitute any individual independent variable, including certain designs involving repeated measurements.4

Permutations, sign flippings, and permutations with sign flippings were performed, either freely or respecting the dependence structure. In each case, 500 shufflings were performed for each of the 500 variables, and the whole process was repeated 500 times, allowing histograms of p-values to be constructed, as well as to estimate the variability around the heights of the histogram bars. Confidence intervals (95%) were computed for the empirical error rates and power using the Wilson method. Significance levels were also compared using Bland–Altman plots, modified so as to include the confidence intervals around the means of the methods. The histograms and Bland–Altman plots are shown in the Supplementary Material.

Power

The evaluations above were used to assess error rates and power according to the degree of non-independence between observations and distribution of the errors. To further investigate how the restrictions imposed by the exchangeability blocks could affect power, other dependence structures were considered to shuffle the data, in addition to the datasets a and b above; these were named c through i (Fig. 6, Fig. 7, Fig. 8). The configuration c corresponds to freely shuffling 11 observations; d corresponds to a small set of 5 sibships with a total of 18 subjects, mixing whole-block and within-block at different levels; e is formed by 15 observations, organised in 5 blocks of 3 observations each, with shufflings being allowed within-block only; f is similar, but with whole-block rearrangements only, and g also similar, but allowing both whole-block and within-block simultaneously; configurations h and i use the family structure of the Human Connectome Project at the time of the hcp-s500 release (more details below): in h, dizygotic twins are treated as a category on its own, thus accounting for the possibility of shared, non-genetic effects within twin pair, whereas in i, dizygotic twins are treated as ordinary, non-twin full siblings. The number of possible permutations and sign flippings for each of these structures is shown in Table 1.

For each of these nine datasets, an artificial effect (signal) was introduced, in the same way as described in the previous section, but here exclusively using independent Gaussian errors and preserving this independence throughout the simulations while still using multi-level exchangeability blocks for shuffling, as if dependencies among the data existed. Power was then compared with what would be observed if the same data were shuffled without the restrictions imposed by the ebs. For each configuration, 100 repetitions were performed, each simulating 1000 variables (as before, each could represent a voxel or vertex in an image). Up to 512 shufflings were used, either permutations, sign flippings, or permutations with sign flippings. Each repetition used a different set of random observations and a different set of shufflings when the maximum number of possible rearrangements was larger than the number of shufflings performed. The significance level was set as. Both the number of permutations and the significance level were chosen so as to allow compatible resolutions of the p-values among runs, allowing a more direct comparison between each case.

Power changes were assessed in relation to what would be observed if the data were shuffled freely, and compared to a measure of the amount of shuffling applied to the data, given the restrictions imposed by the permutation tree. For this purpose, the Hamming distance was used; this distance counts the number of observations that change their position at each permutation (ee) or that change their sign at each sign flip (ise), or both when permutations are performed together with sign flippings. While the Hamming distance cannot be interpreted as a direct quantification of perturbation on the data, it is appropriate to quantify the effect of the shufflings proper, which do not depend on actual data values.

Real data

The ongoing Human Connectome Project (hcp) involves the assessment of about four hundred sibships, in many cases with up to four subjects, and with at least one pair of monozygotic (mz) or dizygotic (dz) twins. The inclusion of additional siblings to the classical twin design is known to improve the power to detect sources of variation in the observable traits. The objective is to have a genetically informative sample as in a classical twin design, enriched with the inclusion of relatives from the same nuclear family. The coefficient of kinship between mz twins is the same for all such pairs, and so are their expected covariance. Likewise, the covariance is the same for all pairs of dz twins. While kinship can be modelled, such modelling is contingent upon various assumptions that may not always be valid, or that can be hardly checked for all the imaging modalities and exploratory analyses that the hcp entails. Instead, such dependence structure can be represented as a tree that indicates which pieces of data can be shuffled for inference, rendering the permutation methods described this far directly applicable to the hcp data, and without the need to explicitly model the exact degree of dependence present in the data. Depending on whether there is interest in considering or not common effects in dizygotic twins, these can be treated as a category on their own, that cannot be shuffled with ordinary, non-twin siblings, or be allowed to be shuffled with them (Fig. 7, Fig. 8).

Virtually all data being collected in the hcp are to be publicly released,5 and at the time of this writing, the available data are the hcp-s500, which includes various imaging and non-imaging measurements for approximately five hundred subjects. Here, measurements of height, weight, and body mass index (bmi) were investigated for positive and negative associations with the cortical area and thickness as measured at each point of the cortex. These traits are well known to be highly heritable, with most studies reporting h2 estimates that are well above 0.70, so that measurements on subjects from the same family cannot be considered independent. [For the heritabilities of height, weight and bmi, see,,,,,; for cortical thickness and area, see,,,,,,, among others.] To confirm the heritability of these traits specifically in the hcp sample, the variance of these traits was decomposed into genetic and environmental components using the maximum-likelihood methods described in, and as implemented in the package Sequential Oligogenic Linkage Analysis Routines — solar (Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, usa). The released hcp data do not include an index that could directly categorise subjects according to a common environment or household. Nonetheless, ignoring these possible effects has the potential to overestimate heritabilities. To minimise this possibility, two models were tested: one in which a common environment term (c2) was not included, and another in which a rather conservative surrogate for household effects was included; such proxy was defined by assigning all subjects sharing the same mother to a common environment. The reasoning is twofold: to account for potential maternal effects, which could affect half-siblings sharing the same mother, but not those sharing the same father, and also considering that, most commonly, children of divorced couples tend to stay or dwell with their mothers for most of the time. To ensure normality, the traits were subjected to a rank-based inverse-normal transformation before estimation. The nuisance variables included in the model were age, age-squared, race and ethnicity, the interactions of these with sex, as well as sex itself. The test statistic, for either h2 and c2, is twice the difference between the log-likelihood of a model in which the parameter being tested is constrained to zero and the log-likelihood of a model in which that parameter is allowed to vary; this statistic (deviance) is distributed as 50:50 mixture of a point mass and a χ2 distribution with one degree of freedom; here we call this statistic 2DLL. For this analysis, 502 subjects with complete data for all these variables were selected (mean age: 29.22, standard deviation: 3.47, range 22–36 years; 296 females; 49 mz pairs, 356 non-mz sibling pairs, 16 half-sibling pairs).

The imaging protocol used for the structural magnetic resonance scans, as well as the steps necessary to construct the surface representation of the cortical mantle, have been described extensively in (see also the references therein); FreeSurfer (Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, ma, usa) was used to generate the surfaces and to obtain cortical thickness measurements; image registration was performed using the Multimodal Surface Matching (msm) framework. The surface area was processed using the methods described in: the area was measured at each face of the white surface, then interpolated using a pycnophylactic method to a common grid (an icosahedron recursively subdivided five times, therefore with 10,242 vertices and 20,480 faces), and finally converted from facewise to vertexwise. Cortical thickness was also resampled to the same resolution, using barycentric interpolation. Both thickness and area were smoothed on the surface of a homeomorphic sphere with 100 mm radius using a Gaussian kernel with full width at half maximum (fwhm) of 20 mm. For these analyses, 5000 permutations were used, and dz twins were considered as constituting a category on their own, and therefore not allowed to be permuted with non-twin siblings in the same family. Nuisance variables were the same used for the heritability analyses described above, plus global cortical surface area and average thickness. Visualisation of imaging results used Blender (The Blender Foundation, Amsterdam, The Netherlands). Sample statistics for the analysed traits are shown in Table 2.

Error rates and power

Despite the differences in the relationship between the observations that constituted datasets a and b, the results were very similar. With errors that were independent and symmetric, i.e., either normally distributed (Gaussian) or kurtotic (Laplacian), the false positive rates (error type i) were controlled at the nominal level (α = 0.05) using unrestricted permutations, sign flippings, or permutations with sign flippings, whenever there were no true dependence between observations or elements of the regressor of interest, that is, when either hϵ2 or hm2 was equal to zero. With both hϵ2 and hm2 higher than zero, however, the conventional test in which the data are shuffled freely became, as expected, invalid. Using instead the shuffling strategy that we propose, that respects the covariance structure present or assumed to exist in the data, the false positive rates were controlled at α, even when the dependence was at high levels. These results are shown in Table 3 (Gaussian) and in the Supplementary Table 1 (Laplacian).

With skewed (Weibullian) errors, sign flippings were generally conservative when hϵ2 or hm2 were equal to zero and the data were shuffled freely. With hϵ2 and hm2 higher than zero, the test not only reversed its conservativeness, but became invalid if flippings ignored the data structure. If, however, the shufflings were performed respecting the restrictions imposed by the relationships among the datapoints, the test was valid in all cases, with its conservativeness maintained. These results are shown in the Supplementary Table 2.

These tables also show the power of each shuffling strategy when there is true signal present. For the cases in which the false positive rate is not controlled, the test is invalid, and as a consequence, considerations of power are irrelevant; in these cases, the values that would represent power are shown crossed by a line. When the data are truly independent, hence unrestricted shuffling could be performed, the proposed restricted permutations caused a slight, yet consistent, loss of power for the datasets a and b. This is revisited in the next section, with the other synthetic datasets.6

Power

For the nine synthetic datasets, a slight, yet consistent loss of power was observed when using the proposed restricted shuffling strategy, compared to the results using unrestricted shuffling when the last was, in fact, possible. These results are shown in Table 4. The loss appears to be larger for the datasets with more involved dependence structures (e.g., dataset d), or when restrictions on permutations are imposed at higher levels (e.g., dataset e), or on sign flippings at lower levels (e.g., datasets f and g). Even so, this is not quite as conspicuous with samples that are just modestly larger (e.g., a and b), or much larger (e.g., datasets h and i, that use the data structure from the hcp).

With exchangeable errors, in which only permutations are performed, power reductions were more noticeable for some datasets and related well to how the data could be disarranged at each permutation, as quantified by the average Hamming distance across the permutations that were performed. This is shown in Table 4, and also visually in Fig. 9. With independent and symmetric errors, in which only sign flippings are performed, the power losses were considerably smaller, and unrelated to the Hamming distance. In the same manner, permutations combined with sign flippings showed power changes that were minimal, and unrelated to the Hamming distance. Moreover, in these cases the resulting power was, for all datasets, higher than for just permutations or just sign flippings.

Table 4 and Fig. 9 show a considerable dispersion of the observed power around the average. In the simulations, this dispersion can be reduced by one order of magnitude approximately just by using the same data and design for all repetitions, varying only the set of shufflings that are performed. Although this reduced dispersion would reflect more accurately the actual variation that different shufflings would cause on a given real experiment, the average power would be dependent on the exact, but random values used for the simulations, and would not be appropriate for the investigation performed here. The magnitude of variations on power as shown does not translate to actual experiments and should not be interpreted as such.

Real data

Summary statistics for height, weight, bmi, global cortical surface area, and global average thickness for the analysed hcp sample are shown in Table 5. The same Table also shows that, consistently with the literature, all these quantities are highly and significantly heritable, even when a conservative surrogate for common environment is included in the model. In fact, the estimated common environment fraction of the variance (c2) was zero for all traits except for height. When the shared environment term is removed from the model, the estimated heritability for height increases to 0.8771 (standard error: 0.0244, 2DLL = 146.9, p-value: 4.1 · 10− 34).

Permuting the data freely to test the hypotheses of correlation between thickness or area and indices of body size, therefore not respecting the structure of the sibships, allowed the identification of a few seemingly significant associations, even after fwer correction across the whole brain, and considering that both positive and negative tests were being performed. These regions, shown in Fig. 10, are (1) the left anterior cingulate for a positive correlation between height and cortical surface area, (2) the right orbitofrontal medial cortex for a positive correlation between thickness and bmi, (3), the right temporal pole, at the confluence of the inferior temporal gyrus, for a negative correlation between thickness and body weight, and (4) the right inferior temporal gyrus for a negative correlation between thickness and height. All these regions are very small, two of them comprising just one vertex at the resolution of the surfaces. However, using the proposed multi-level permutation strategy, in which shufflings only happen within siblings of the same type, and in which families with identical structure are allowed to be permuted as a whole, therefore respecting the kinship structure, all these findings became no longer significant. Supplementary Table 3 shows the minimum (most significant) p-value throughout the brain for both unrestricted and restricted permutation.

Error rates and power

The proposed multi-level shuffling strategy controlled the false positive rate at the nominal level in all configurations evaluated. With the only exception of sign flippings in the presence of skewed errors, which clearly violates assumptions, the empirical distribution of p-values was uniform, as desired, whenever shufflings respected the dependence structure present in the data; ignoring the dependence resulted in inflated error rates, rendering the test invalid. Having dependence in both data and model may seem unusual, but in fact, this is a quite common scenario, as exemplified with the data from the hcp.

The guaranteed validity and exactness of p-values came, however, at the price of a small, yet noticeable and consistent reduction in power, that related to the complexity of the dependence structure and the ensuing restrictions on exchangeability. This can be understood by noting that the restricted permutation strategy does not disarrange the data as much as the unrestricted shuffling, with the consequence that the statistics computed after permuting the data may not be as distant from the statistic computed from the unpermuted data. With sign flippings, the power losses were smaller, and unrelated to the Hamming distance, presumably because even changes seemingly small, such as a single sign swap, can cause large perturbations on the shuffled data that are sufficient to minimise reductions on sensitivity. Permutations combined with sign flippings showed minimal power changes that were also unrelated to the average Hamming distance, and with losses that were smaller than for just permutations or just sign flippings, suggesting that when both ee and ise are valid for a given model, permutations with sign flippings can allow maximum efficiency.7

Although the diminished sensitivity could suggest that the multi-level permutation strategy would be “conservative”, this is not the case, as can be attested by the exact control over error rates. This apparent incongruity can be understood through the Bland–Altman plots shown in the Supplementary Material, that show that the differences in uncorrected p-values between both strategies is largely outside the margins of the confidence interval in both directions, suggesting that, under the null, variations in p-values can go in any direction when the strategies are compared. Nonetheless, in the presence of signal, or when the p-values are corrected for multiple testing using the distribution of the largest statistic across variables (such as voxels), the p-values for the restricted strategy tend to be stochastically larger than those for the free shuffling.

The restrictions imposed on the possible rearrangements that can be performed, with the consequent reduction in the number of possible permutations, as well as the lessened sensitivity, could be seen as undesirable, but in fact, such restrictions establish a set of rules under which permutation inference can be performed in settings where otherwise it would not possible without appealing to often untenable assumptions, or that would not be possible at all. Simple permutation, if performed, would create data that could be impossible to be observed in practice, and thus, that should not be used to construct the reference distribution to test the hypotheses of interest. Moreover, the stronger the dependency is between observations, the fewer genuinely independent pieces of information are available to test a given hypothesis; in this scenario, smaller power does not appear unexpected.

Body size and cortical morphology

Height, weight, and bmi are known to be highly heritable in general, and were so for the hcp sample. Likewise, the heritability for global cortical surface area and average thickness are known to be heritable, and were found as such in the sample analysed. All these traits remained highly heritable even when a potential confound — a surrogate for household and maternal effects — was included. Even if estimated heritability were reduced, common effects would still cause the observations not to be independent. The fact that for all these traits there is a strong dependence between the observations implies that a permutation test that ignores the relationship between observations would not be valid, by violating exchangeability.

Indeed, the test that shuffled the data freely identified a few positive and negative localised significant associations between indices of body size and cortical area and thickness, even after fwer correction considering all tests in both hemispheres and the fact that positive and negative hypotheses were being tested. None of these areas were found to be significant if the test used only permutations that respected the structure present in the data, in the multi-level fashion, suggesting that these findings are likely false positives. None of the regions implicated were reported in previous studies that investigated relationships between indices of body size and cortical morphology that we could identify. It should be conceded, however, that not all these studies used the same methods, with some having analysed grey matter volumes in voxel-based representations of the brain, and some, despite using surface-based methods, performed analyses in macroscopic regions, as opposed to at each point in the cortical mesh. Still, as the simulations demonstrated, the violation of the exchangeability assumption makes the free permutation prone to inflated amounts of error type i if the observations are not independent, and the absence of similar findings from the literature supports the likelihood that these seemingly significant findings are not genuine, being instead false positives.8

Another aspect is that, although fwer-correction was applied considering the multiplicity of vertices in the mesh representation of the cortex and the two contrasts (positive and negative), no correction was applied considering that overall six tests were performed (three independent variables versus two dependent variables); fwer-controlling procedures that would take into account the non-independence between these tests are currently not available. Using Bonferroni correction, the results using the free permutation, which are likely false-positives as discussed above, disappear. Since most studies — and in fact, most of those referenced in the previous paragraph — investigated only the relationship between one independent versus one dependent variable, for which no such correction is necessary, the results shown emulate well the risk of false positives in similar, real studies.

Applications and other considerations

In addition to the above examples, and most clearly, with a direct example application for the hcp data, the multi-level permutation strategy can be considered for repeated measurements designs in which within- and between-subject factors are tested in the same model or contrast, such as for a continuous regressor. A direct comparison of the power observed for datasets e, f and g, using permutations only, shows that even with the same number of subjects, the combination of within-block with whole-block permutation can be more powerful than each of these used in isolation. Moreover, the strategy can also be considered when not all measurements for a given subject are available, as long as compound symmetry within subject remains valid, without the need to exclude entirely the data for subjects as would be the case for whole-block permutation.

As experiments are planned considering strategies for subsequent analyses, the use of permutation tests can be included among the tools available, especially given its simplicity and, as demonstrated here and in a large body of literature, flexibility to accommodate designs and data that can be quite complex. Adequate planning includes ensuring that assumptions for permutation tests are met from the beginning, such as that the random errors of the instrument are stable along time, and do not vary with the values they measure, that the observations if not independent, possess a dependence structure that can be accommodated in a framework as the one shown here, and that observations, if not homogeneous, can be broadly qualified into a few number of variance groups.

Indeed, regarding vgs, the compatibility of these with the blocks ensures the feasibility of permutation tests, but it also allows that the necessary assumptions are reduced to a minimum: instead of requiring that all observations are homoscedastic (strong), the maximum possible amount of heterogeneity of variances that could still permit the shuffling as indicated by the blocks (weaker assumption) can be allowed. In this case, homogeneity would still be there, although not across all and every observation, just the minimal amount necessary so that the experiment can still be analysed. These considerations may not be relevant if the recruiting process, experimental conditions or data collection can guarantee that the same variance is homogeneous, but may be necessary when the data collection or samples are not under direct control of the researcher (e.g., reanalysis of past experiments, or census data).

Conclusion

The proposed multi-level block permutation effectively controls the false positive rate, even in the presence of strong dependence between observations, and can be used as a general inference tool when the dependence structure can be organised in blocks, hierarchically if necessary. There is an unavoidable loss of power due to reduced scope of shuffling, although in large datasets, with relatively complex dependence structure, such as the hcp, this loss is expected to be quite small, especially if permutations can be combined with sign flippings.

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