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- Journal List
- PLoS Genet
- v.7(3); Mar 2011
- PMC3048375

# Testing for an Unusual Distribution of Rare Variants

^{#}

^{1,}

^{2,}

^{*}Manuel A. Rivas,

^{#}

^{1,}

^{2}Benjamin F. Voight,

^{1,}

^{2}David Altshuler,

^{2,}

^{3,}

^{4}Bernie Devlin,

^{5}Marju Orho-Melander,

^{6}Sekar Kathiresan,

^{1,}

^{2,}

^{7,}

^{8}Shaun M. Purcell,

^{2,}

^{9}Kathryn Roeder,

^{10,}

^{¶}

^{*}and Mark J. Daly

^{1,}

^{2,}

^{¶}

^{*}

^{}

^{1}The Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America

^{2}The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, United States of America

^{3}Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America

^{4}Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America

^{5}Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America

^{6}Department of Clinical Sciences Malmö, Diabetes and Cardiovascular Diseases, Genetic Epidemiology CRC, University Hospital Malmö, Malmö, Sweden

^{7}Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, United States of America

^{8}Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America

^{9}Psychiatric and Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, United States of America

^{10}Department of Statistics, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America

^{#}Contributed equally.

Conceived and designed the experiments: BMN MAR BFV DA BD SMP KR MJD. Performed the experiments: BMN MAR KR MJD. Analyzed the data: BMN MAR KR MJD. Contributed reagents/materials/analysis tools: BMN MAR MOM SK SMP KR MJD. Wrote the paper: BMN MAR KR MJD. Commented on the manuscript and aided in the development of the method: BFV BD. Commented on the manuscript and aided in the development of the methodological idea: DA. Contributed APOB data: MOM SK.

## Abstract

Technological advances make it possible to use high-throughput sequencing as a primary discovery tool of medical genetics, specifically for assaying rare variation. Still this approach faces the analytic challenge that the influence of very rare variants can only be evaluated effectively as a group. A further complication is that any given rare variant could have no effect, could increase risk, or could be protective. We propose here the C-alpha test statistic as a novel approach for testing for the presence of this mixture of effects across a set of rare variants. Unlike existing burden tests, C-alpha, by testing the variance rather than the mean, maintains consistent power when the target set contains both risk and protective variants. Through simulations and analysis of case/control data, we demonstrate good power relative to existing methods that assess the burden of rare variants in individuals.

## Author Summary

Developments in sequencing technology now enable us to assay all genetic variation, much of which is extremely rare. We propose to test the distribution of rare variants we observe in cases versus controls. To do so, we present a novel application of the C-alpha statistic to test these rare variants. C-alpha aims to determine whether the set of variants observed in cases and controls is a mixture, such that some of the variants confer risk or protection or are phenotypically neutral. Risk variants are expected to be more common in cases; protective variants more common in controls. C-alpha is sensitive to this imbalance, regardless of its origin—risk, protective, or both—but is ideally suited for a mixture of protective and risk variants. Variation in APOB nicely illustrates a mixture, in that certain rare variants increase triglyceride levels while others decrease it. The hallmark feature of C-alpha is that it uses the distribution of variation observed in cases and controls to detect the presence of a mixture, thus implicating genes or pathways as risk factors for disease.

## Introduction

High throughput sequencing of the human genome is now a reality: recent advances in sequencing technology now permit near complete ascertainment of genetic variation, including rare variants (<1% population frequency), across large portions of the genome in thousands of individuals. While this in principle can reveal the role of each gene in every medical phenotype, the analytic challenges are profound. Of particular concern are genetically complex common diseases for which the role of any gene is expected to be quite modest and an individual rare variant would have relatively small impact on the common endpoint. Under this scenario there would be little power when testing one variant at a time, as in traditional association testing. For example, while in African Americans low-frequency variants in PCSK9 can have a substantial effect on serum low-density lipoprotein cholesterol (LDL-C) [1], these variants influence risk or protection to myocardial infarction by only a factor of 2 [2], [3]. In such instances, rare variants will almost never stand out as associated individually, particularly when all variation in the genome is measured and tested in an effort to discover novel loci, rather than simply evaluate existing candidate genes.

Recently published methods show that power to detect rare risk variation can be greatly enhanced by combining information across variants in a target region, such as a gene or exon, when multiple variants influence phenotype. The “cohort allelic sums test” (CAST) [4], [5] and “Combined Multivariate and Collapsing (CMC) method” [6] use this approach. CAST contrasts the number of individuals with one or more mutations between cases and controls. Like CAST, in CMC all rare variants are collapsed and treated as a single count for analysis with common variants in a multivariate test. CMC permits a coherent test for common and rare variants (rare being defined arbitrarily, but usually at 1%). Madsen and Browning [7] introduced a non-parametric weighted sum test in which rare variants “are grouped according to function (e.g. gene), and each individual is scored by a weighted sum of the mutation counts.” The incorporation of weights improves the power of the test, and would be especially powerful when most of the rare variation is functionally relevant. While each of these rare variant tests differs in form, each seeks to assess the overall genetic burden due to rare variants, hence we call them “burden tests”. By design, they implicitly assume that all variation affecting phenotype acts in the same direction.

Even in a gene harboring phenotypically relevant variation, however, many variants will be phenotypically neutral. Indeed, the target region could include a handful of rare Mendelian mutations that cause disease, some variants that moderately increase or decrease risk, along with numerous variants of no effect. To gain insight into a new model for analysis, it is helpful to think of a coin toss associated with each variant. If the variant is phenotypically neutral, the coin is fair and the variant is as likely to appear in a case as it is in a control. In contrast, risk variants correspond to biased coins and are more likely to be observed in cases. Similarly, protective variants correspond to coins biased in the opposite direction and are more likely to be observed in controls, particularly if they are selected. See Figure 1, which illustrates this scenario and motivates a new testing procedure. Burden tests seek to determine if the coin is biased, on average, across all variants. Invariably they include phenotypically neutral variants in the burden score, which diminishes the power of the test. In addition, there are many examples in which gain or loss of function in the same gene have opposite effects on phenotype [8]-[10].

**Mixtures of biased coins in a set of largely neutral coins generate substantially increased variances compared to uniform coins with the same bias.**

Table 1 illustrates the challenges by presenting novel sequencing of the gene APOB (Apolipoprotein-B) in 96 individuals who have high triglycerides and 96 individuals who have low triglycerides. Do rare variants in APOB influence lipid levels? Figure 2A illustrates the distribution of APOB variants amongst high/low individuals. Notice the unlikely occurrence of variants with 6:0 and 0:6 counts out of fewer than 20 variants discovered. A test that incorporates this increase in variance, or *overdispersion*, could in principle give better power. This observation suggests a novel approach to the problem: tally the number of copies of each variant in cases, relative to the number copies in controls, and evaluate overdispersion in the set of counts. Overdispersion in this setting measures an increase from the expected binomial variance, driven by a subset of variants seen preferentially in cases or controls (the biased coins in the example in Figure 1).

A well-established and powerful test for the presence of a mixture of biased and neutral coins is the C-alpha score-test [11], [12]. We describe here the adaptation of this test for the analysis of sequence level case-control data and demonstrate its performance in a variety of simulated and actual data examples. We then move to a few key assumptions of C-alpha and how to accommodate realistic scenarios that violate those assumptions. Finally, we propose extensions of the method.

## Methods

### C-alpha test

To illustrate where the information for C-alpha originates, consider a standard balanced case-control study. If the target region has no alleles associated with the phenotype, then the distribution of counts should follow a binomial distribution, indexed by n, the total number of copies of an observed variant. In Figure 2 we contrast the expected distribution of binomial counts (background) with observed counts (foreground) for three phenotypes. Each row of the triangle corresponds with a different value of n. The number of distinct variants observed for panel (b) is *m*=14 with *n* ranging from 2 to 40. The number of variants with *n* copies, *m*(*n*), varies from row to row: *m*(2)=2, *m*(3)=3, *…, and m*(40)=1. C-alpha detects unusual numbers of counts falling toward the outer edges of the triangle; In Figure 2A, one variant is observed exclusively in cases (6:0) and another in controls (0:6). Both configurations generate overdispersion. Any mixture of binomials leads to overdispersion, which can be detected by a one-sided test. This is the fundamental basis of C-alpha. See Figure S1 for further illustration.

We have tailored the C-alpha score test so that it is suitable for testing a set of rare variants for association. The binomial (*n*,*p*) distribution evaluates the probability of observing a particular variant *y* times in the cases out of *n* total, assuming the rare variants are distributed at random across the subjects. For variants seen twice (doubletons) in a balanced sample of cases and controls (*p*=0.5), we expect *y* to be 0, 1 and 2 with probability ¼, ½ and ¼, respectively. We typically will observe a higher proportion of doubletons with *y*=2 and/or *y*=0 than expected, if some variants are detrimental or protective. For each variant, there will be insufficient information from which to draw firm conclusions about association. C-alpha can be used to detect a pattern across the full set of rare variants in the target region. For the i'th variant, observed *n _{i}* times, we assume y

_{i}is binomial (

*n*,

_{i}*p*). Under the null hypothesis,

_{i}*p*=

_{i}*p*(say ½ if cases and controls are equal in number and we expect rare variants to fall in either sample at random). The alternative hypothesis is that

_{0}*p*follows a mixture distribution across the

_{i}*m*variants,

*I*=1,…,m, with some variants detrimental (p

_{i}>p

_{0}), some neutral, and some protective (p

_{i}<p

_{0}).

The C-alpha test statistic *T* contrasts the variance of each observed count with the expected variance, assuming the binomial distribution

To standardize this quantity we require *c,* the variance of *T*:

in which *m*(*n*) is the number of variants with *n* copies, and denotes the probability of observing *u* copies of the i'th variant assuming the binomial model.

The resulting test statistic is defined as . We reject the null hypothesis when *Z* is larger than expected using a one-tailed standard normal distribution for reference. See the Text S1 for a derivation of the C-alpha test.

Let's examine data from two genes, *PCSK9* and *APOB*, in which rare variation is known to affect lipid levels (LDL and Triglycerides), and treat the phenotypic extremes as binary traits (i.e. high lipid levels are cases and low lipid levels are controls). The previously reported *PCSK9* data result from sequencing its coding regions [1] in 128 individuals with extremely high and 128 with extremely low plasma LDL-C levels. Applying C-alpha produces a significant association (p-value =0.0023.) The loss of functional variants (C679X, Y142X) in *PCSK9* are associated with a 28 percent reduction in mean LDL cholesterol and an 88 percent reduction in the risk for coronary heart disease [2]. The gain of function variant (H553R) in *PCSK9* is associated with increased plasma levels of LDL-C [13]. The pattern of overdispersion is also apparent when examining the genotype counts derived from a pooled sequencing experiment of coding regions in *APOB* (Figure 2A). We do not report a P-value for the *APOB* example, as these data are pooled and so we cannot assess significance empirically. In this case DNA from 96 individuals with extremely high triglyceride levels was pooled, as was DNA from 96 individuals with extremely low triglyceride levels [3], and these two pools were sequenced. Another example of rare variation predisposing to disease is clearly evident from a study of Crohn's disease (Figure 2B). Association of low frequency variation at NOD2 (excluding two common coding variants R702W and insCfs1003) is demonstrated in 350 Crohn's disease cases and 350 GWAS matched controls with a P-value of less than 10^{−6} from individual level data.

### Estimation of mixtures

It is additionally possible to estimate the underlying mixture model from the distribution of variants used for C-alpha testing. For instance, if the target region includes risk variants, phenotypically neutral variants, and variants that engender a modest protective effect, then a 3-component mixture will fit the data corresponding to the 3 genetic components. Whenever C-alpha shows significance, we can estimate the number of mixture components and the posterior probability that a particular variant is detrimental or protective using the EM algorithm (see Text S1 and Figure S4).

### Singleton counts

A variant observed only once provides no direct information about over-dispersion; however the distribution of singletons as a group reflects on the question of association between the target region and phenotype. Singletons can be pooled into a single binomial count that can be included in the C-alpha test. This treatment of singletons, which is essentially identical to a burden test (see Text S1 on mixtures of biased and unbiased coins and Figure S1), allows robust integration of singletons. However, it can only be informative if the majority of the singleton variants have effects in the same direction. Other approaches to addressing singleton variants in parallel with C-alpha are considered in the discussion.

### Simulation experiments

We conduct two main sets of simulations to compare C-alpha with Li and Leal burden tests and Madsen and Browning's test. Tests proposed by Li and Leal are all built around a regression model, predicting phenotype based on recoding of rare variation. For Li and Leal's approach, we sum the number of rare variants in the region for each individual as the predictor. For Madsen and Browning, the coding of variation is similar to the sum of rare variants, but a weighting scheme based on the inverse of the control allele frequency is included. The test statistic is evaluated as a nonparametric rank sum test in which each individual is scored by a weighted sum of the mutation counts. We also include a variable threshold model, which is an implementation of a burden test that selects the threshold for inclusion of variants by optimizing the test statistic. Specifically, this burden test is calculated at all allele frequency cutoffs. The test statistic is then defined by the maximum of the test statistics for all cutoffs. The distribution of the test statistic is obtained empirically by random permutation of case/control status and recalculation of the test statistic. This approach is described in Price et al [14]. In addition to these simulations under the alternative hypothesis, we present a series of simulations under the null hypothesis to investigate the small sample properties of the test statistic. For each kind of simulation and for all test statistics, we assess significance empirically, by using permutation, as described previously. For each test, we permute 50,000 times to ensure accurate assessment at P-value threshold of 0.001. Singletons are treated in accordance with the original specification for each method. For C-alpha we pooled the singletons into a single observation.

We first present a set of simulations for a population genetics model that incorporates selection [15], and generates data that matches the empirically observed allele frequency distribution derived from sequence data. This approach implements a demographic model by which variants in the region are in linkage equilibrium (simulated, not forced) and mutations have selection coefficients above 10^{−3}. Two genes were simulated, and the mean liability value for an individual differed as a function of the number of rare alleles occurring at these genes [14], [15]. For individuals who have no rare variants, liability was simulated using a N(0,1). Each functional variant increased the mean of the liability distribution by 0.25, while maintaining the variance of 1. Each simulated gene was 1.5 kb long, with a mean and variance of number of variants at ~38.5 and 40 respectively. Of the variants observed, 52% were functional. Note that this constitutes a favorable scenario for frequency weighted burden testing as the burden continues to increase with additional variants and the frequency of the functional variants is generally kept lower. To expand these simulations, we then randomly assigned a direction of effect for these variants, according to a range of mixing proportions (0 to 50% probability of assignment of protective in 10% increments).

For the second set of risk simulations, we assume a model with a disease prevalence of 1%, 50 sites in the region of analysis with allele frequency between 0.025% and 0.5% (this distribution is similar to that observed from the Crohn's data). These sites are variable in the population, but may be invariant in any given simulation, as they are probabilistically assigned for each member of the sample. Of these 50 variants, 6 are chosen at random for each simulation to affect the phenotype (regardless of whether they are present in the dataset), and each variant explains 0.1% of the variance of the disease under a liability threshold model (i.e. 2p [1-p]a^{2}=0.001, where p is the risk allele frequency and a is the effect on mean liability [16]). The model assigns higher penetrance to rarer alleles, yet no alleles are so highly associated that they would be readily detectable by single variant analyses (see Text S1 and Figure S3 for the relationship between odds ratio and frequency). Furthermore, the functional variants may be singletons in the final dataset, especially if they have a very rare population allele frequency.

Three scenarios are explored: all 6 variants confer risk; 3 variants confer risk and 3 variants confer protection; and all 6 variants confer protection. We also consider two different study designs: 1,000 cases (individuals who exceed the threshold on the liability distribution) and 1,000 controls (individuals selected for absence of disease); and 1,000 cases and 1,000 *selected* controls, such that the controls are selected to be in the bottom 1% of the latent liability distribution. The latter strategy mimics experimental designs used for quantitative phenotypes.

### Small sample properties

A third set of simulations explores behavior of test statistics under the null hypothesis to determine whether the type I error rate is well calibrated for C-alpha. Like many tests, C-alpha relies on asymptotic properties consistent with the central limit theorem (CLT). Specifically, the test statistic converges to a normal distribution under the null hypothesis as the number of variants tends toward infinity, with convergence being potentially faster if the frequency of all variants is similar. Thus, we varied both the number of variants and the distribution of allele frequencies to explore type I error. For these simulations, we drew N variants from the empirically observed allele frequency distribution used in the second set of simulations above and performed 25,000 replicates for each value of N.

## Results

### Results of power comparisons

From simulation results evaluating power (Figure 3), C-alpha shows comparable or slightly better power than burden testing in the situation where all effects are in the same direction, and much greater power when protective and risk variants exist in the test set. Thus the mixture approach shows good power for a much broader set of scenarios without sacrificing power when unidirectional burden testing is also effective.

### Results assessing asymptotic properties

Simulation results (Table 2) demonstrate that the tails of the distribution are somewhat heavier than the assumed normal distribution when the number of variants is small, but as expected, they approach that of the assumed distribution when the number of variants increases. Additionally, in simulations performed under a single allele frequency, the test achieves asymptotic behavior considerably more quickly. To estimate significance accurately when small numbers of variants are under consideration, we therefore recommend a standard permutation procedure whereby we randomly reassign cases and controls and recalculate the test statistic (just as would be applied in any association scenario involving small sample numbers and/or frequencies). Regardless of the slightly heavy tails for small numbers of variants, the test statistic itself is still a fast, effective screen for identifying potential regions of interest in the genome. We note that our power calculations and any examples involving sequencing of individual samples use p-values obtained by permutation of case-control status. Additionally, C-alpha assumes independence of each observed variant. Permutation yields appropriate p-value distributions even in the presence of LD between variants because case-control permutation maintains the LD relationship between all SNPs [17].

## Discussion

We have demonstrated here the adaptation of the C-alpha test statistic and its broad applicability to medical sequence data on a gene or pathway level. The approach, distinct from more traditional burden testing, has several advantages over the previously proposed test statistics. Its primary advantage is sensitivity to risk and protective variants in the same gene or pathway. Yet, even if the effects of rare alleles are uniformly in one direction, such as increasing risk, C-alpha maintains comparable power to burden tests. Grouping genes together into pathways and testing rare variants falling into these groups of genes could provide greater statistical power and biological insight into the functionally relevant processes affecting the phenotype of interest. In such groups the presence of both risk and protective variants is even more likely. As demonstrated here, the C-alpha test is well calibrated to incorporate such divergent effects on risk. Moreover because it is a single degree of freedom test with normal asymptotic properties, C-alpha enhances power and allows for rapid and straightforward calculation.

As with other burden-style tests, C-alpha is designed for situations in which numerous rare variants are observed in the target region. We recommend permutation testing for accurate significance estimation in scenarios where the asymptotic behavior is not assured - in particular, for small numbers of variants, when LD is present, or when the test is driven by a single more common variant. In this latter scenario, as in the example of NOD2, it will likely be desirable to analyze the more common variant with Fisher's exact test and to reanalyze the remaining rarer variation to search for additional signal.

While singleton variants can be combined in C-alpha, it seems reasonable to consider a distinct analysis of singletons in a more biologically motivated fashion. For example, when a truly rare and fully penetrant mutational origin is suspected, one might focus on variants seen only in cases and not seen in external reference data such as from 1000 Genomes Project. One might then further filter the identified variants to leave only putatively deleterious non-synonymous, splice and obvious loss of function variants and then compare the rate of these to the parallel set found in controls only. Such a Mendelian-style analysis (already successfully applied in several cases such as Miller syndrome [18]), focuses predominantly or exclusively on singleton variants and is almost completely independent of the complementary C-alpha analysis applied to variants seen twice or more in a study. For a polygenic disease, it is reasonable to predict that each of these models could be relevant for different genes (and in some cases, such as *APOB*, the same gene). Thus complementary and independent analyses may be a desirable approach to surveying large, exome-scale datasets.

As with any statistical test, the presence of confounders can seriously bias the results. For instance, we have demonstrated that population stratification has a significant impact on rare variation tests. C-alpha assumes cases and controls have the same balance of ancestry, because the distribution of rare variants likely depends on ancestry. Otherwise unequal representation could increase the rate of false positives for any rare variant test. It is important to note that the balanced sampling assumption is not equivalent to requiring that samples be homogenous. Balanced sampling requires solid experimental design. While statistical methods for controlling for bias can be effective, proper study design is far preferable. If a large set of genotypes were available, such as from a genome-wide association (GWA) study, principal component analyses and related procedures can be used to match or control for ancestry [19]–[21]. For well-matched case-control samples, under the null hypothesis, it is reasonable to assume the distribution of rare variants is independent of case/control status; i.e., a variant is as likely to be identified in a case as a control. One approach to determining whether the assumption of balanced ancestry is violated is to calculate the number of rare synonymous variants observed in cases versus controls across the sequenced regions. If there is a substantive difference between cases and controls in the number of synonymous variation, one explanation is that the matching of ancestry between cases and controls was not successful. If the deviation is modest, that implies that the level of ancestral mismatching is in all likelihood modest. One other major source of bias is differential genotyping bias. For sequencing experiments, variability in coverage and variant discovery between cases and controls can behave similarly to population stratification if such errors are not balanced between cases and controls. As with population structure, appropriate balance of subjects to control for technical variability before analysis should insulate sequencing experiments from major bias, yet subtle excess variability might persist. For well designed studies we propose that Genomic Control [22] will help to correct for the effects of minor stratification and technical variability (for details, see Text S1 and Figure S2).

More generally, the choice of target region and set of variation affects power. A test based on all potentially functional variants (non-synonymous, splice, nonsense, etc.) within a single gene will often be effective as it strikes a balance between sufficient numbers of variants and the enrichment of functional variation. In contrast, a single exon is not likely to have enough variants for the test to be powered adequately or to achieve asymptotic properties and, while including introns and synonymous variants would dramatically increase the number of variants, the expectation is that the vast majority of these variants will be phenotypically neutral and thus will mute the signal. Alternatively, a group of exons from related genes (e.g., a biological pathway) could be analyzed jointly. The test would then determine if some unspecified variants in the pathway are associated with the phenotype via a deviation from the expected distribution of variation. Using this strategy, if several of the genes have an effect, then the power will be enhanced; however, if only one gene in the pathway has an effect, including the other genes in the test will reduce power to detect the effect. For target regions that do show evidence of association, using a nonparametric mixture model we can estimate the distribution of *p _{i}* across variants and estimate the posterior probability the i'th variant is detrimental or protective [23]. In the application to a pathway of genes, one is more likely to uncover both risk and protective variants, making the proposed test even more desirable.

Selecting a subset of variants, as suggested above, is just one form of weighting variants in the analysis. C-alpha allows for valid weights to be incorporated into the calculation of the test statistic (see Text S1). Tests that up-weight variants based on allele frequencies find that power can be improved, if there is a relationship between allele frequency and effect size [7]. However, we found that using the allele frequencies derived from the experiment bias the test. The 1000 Genomes Project provides an independent source for weights for allele frequency weighting. Alternatively, if weights are obtained from the data at hand, a permutation procedure can be used to obtain P-values. Aside from allele frequency, bioinformatic tools that predict the functionality of a variant offer another source for weights. Many computational tools classifying coding variants regarding impact on protein function are already published *In Silico Funcitonal Profiling* [24] POLYPHEN [25], SIFT [26], SNPs3D [27], and Pmut [28]. For example, for POLYPHEN the larger the position-specific score the more likely the substitution is deleterious and applying such weights to each variant in C-alpha might further enhance power. Similar tools are available to score functionality for consensus transcription factor binding sites (TFSEARCH, MATINSPECTOR) and 3’-UTR (ASTRA) [29].

Sequencing technology will continue to develop and reduce in cost for the foreseeable future. Large medically-focused sequencing efforts involving thousands of exomes or whole genomes are now underway and are introducing a host of novel computational challenges not encountered in GWAS and previous large-scale medical genetics studies. By enabling powerful analyses of genes and pathways, without concern for effect direction, C-alpha promises to be a flexible and powerful approach for the identification of functionally relevant regions from experiments involving deep sequencing.

## Supporting Information

#### Figure S1

The four panels show the distribution of the mean and 2*variance of mixtures of binomial distributions under the following set of simulation scenarios. For each set we start with a 50 random draws of size 2 from a binary variable with equal probability of each outcome plus 10 "spiked-in variants" and compare that to 60 random draws of size 2. The spiked-in variants are either all protective (10 0/2's), all risk (10 2/0's) or a mixture as indicated in the title of each panel. The distributions of mean and 2*variance is shown in each panel, with black and blue representing the mean and 2*variance of the null simulations and red and yellow representing the mean and 2*variances of the simulations with spiked in draws. Including a subset of variants with a protective and/or detrimental effect increases the variance of the overall data in a way that is not described by shift in the mean number of alleles in cases (see also Figure 1). C-alpha is sensitive to this increase because it compares the observed variance of the data with the expected variance under the binomial model.

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#### Figure S2

(A) Distribution of p-values under the null hypothesis of no disease association. The distribution of 1,000 p-values under the null hypothesis is consistent with a uniform distribution. The simulations were performed using 1,000 case versus 1,000 control individuals. (B) Distribution of p-values evaluated over exons in a pooled sequencing experiment. We artificially induce inflation to the overall test statistic by including an African American pool, which differs in allele distribution.

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#### Figure S3

The relationship between the strength of the effect and the population minor allele frequency of the locus where the variance explained is fixed for all loci. The rarer the variant, the stronger effect it has on phenotype.

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#### Figure S4

We simulate mixture outcomes for each of the three fixed mixture components, protective (red diamonds), risk (green triangles), neutral (blue triangles). We demonstrate that the Expectation Maximization algorithm, outlined in Text S1, performs well and is able to accurately estimates the simulated mixture components. The proposed EM algorithm can also be used to determine posterior probabilities of belonging into each of the components for each of variants observed.

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## Acknowledgments

We thank Eric Lander, Nick Patterson, and Mark DePristo for useful feedback and comments on the manuscript. We thank Shamil Sunyaev, Alkes Price, and Grigory Kryukov for sharing and discussing population genetic simulations. We thank Helen Hobbs and Jonathan Cohen for PCSK9 sequencing data. We thank Christine Stevens, Candace Guiducci, Noel Burtt, Stacey Gabriel, and the Genome Sequencing Analysis Platform at the Broad Institute for their work on pooled sequencing studies from which illustrative examples were shown. We thank Su Chu for preparing the graphics.

## Footnotes

The authors have declared that no competing interests exist.

This work was supported by NIH grants HL087676, EY11309, NS059727, and DK072041; NIH/NEIHS grant NS059727; NIH/NHBLI grants DK072041 and HL087676; NIH/NIMH grants NS059727, MH057881, MH089025, and MH089208; and Autism Speaks grant for the Autism Genome Project. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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