Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Distribution-based measures of tumor heterogeneity are sensitive to mutation calling and lack strong clinical predictive power


Mutant allele frequency distributions in cancer samples have been used to estimate intratumoral heterogeneity and its implications for patient survival. However, mutation calls are sensitive to the calling algorithm. It remains unknown whether the relationship of heterogeneity and clinical outcome is robust to these variations. To resolve this question, we studied the robustness of allele frequency distributions to the mutation callers MuTect, SomaticSniper, and VarScan in 4722 cancer samples from The Cancer Genome Atlas. We observed discrepancies among the results, particularly a pronounced difference between allele frequency distributions called by VarScan and SomaticSniper. Survival analysis showed little robust predictive power for heterogeneity as measured by Mutant-Allele Tumor Heterogeneity (MATH) score, with the exception of uterine corpus endometrial carcinoma. However, we found that variations in mutant allele frequencies were mediated by variations in copy number. Our results indicate that the clinical predictions associated with MATH score are primarily caused by copy number aberrations that alter mutant allele frequencies. Finally, we present a mathematical model of linear tumor evolution demonstrating why MATH score is insufficient for distinguishing different scenarios of tumor growth. Our findings elucidate the importance of allele frequency distributions as a measure for tumor heterogeneity and their prognostic role.


A major challenge for predicting clinical outcome to cancer treatment is the heterogeneity of cell populations within each tumor, as intratumoral heterogeneity is increasingly being associated with metastasis and resistance to therapies1,2,3,4. Intratumoral heterogeneity develops from mutations in cells and the relative growth advantages they confer to their descendant populations5,6. To better understand this phenomenon, multiple research groups have developed methods for the challenging problem of estimating tumor cellular composition from bulk tumor sequencing data7,8,9,10,11,12,13. These methods rely on the allele frequencies of mutations in each cancer, with low allele frequency mutations providing information on small subclones and high allele frequency mutations providing information on large subclones. Factors such as ploidy, copy number, and tumor purity can also affect this inference. In particular, aneuploidy in DNA mixtures has been associated with poor subclonal inference14. Still, accurate measures of allele frequencies are central for evaluating subclonal heterogeneity and its clinical implications.

Increased heterogeneity has been theorized to lead to worse patient survival due to the increased potential for resistant populations15,16,17, but it remains unclear if current measures of tumor heterogeneity are sufficient to resolve such an effect. Prior studies have attempted to determine this relationship. For example, Rocco et al.18 used MATH score, a measure of the width of the allele frequency distribution, as a proxy for tumor heterogeneity and observed poorer survival for head and neck squamous cell carcinoma (HNSC) in patients with higher MATH score. More recently, Morris et al.19 found associations between heterogeneity and survival in several cancers using a multivariate regression of MATH and other variables versus survival. However, a key caveat is that all heterogeneity measures, including MATH, are affected by the accuracy of mutation calls. Many studies have shown that cancer mutation calls can differ substantially depending on the algorithm used for their determination20,21,22,23. In order to verify if heterogeneity impacts survival, it is necessary to quantify the robustness of allele frequency distributions to mutation callers as well as the robustness of their relationship to survival.

Allele frequency distributions also provide information on the evolutionary processes in tumors, which remain poorly understood. While a variety of intratumoral evolutionary models have been proposed24,25,26,27, the impact of allele frequency accuracy on evolutionary inference has not been substantially explored. Determining the robustness of allele frequency distributions will elucidate this problem.

In this paper we study the robustness of allele frequency distributions and their relevance to patient survival. To the best of our knowledge this is the first study which explores sensitivity of these distributions and their clinical prognostic power to different mutation calling methods. We call single nucleotide variations (SNVs) from 11 cancer types in The Cancer Genome Atlas (TCGA) using three common mutation callers: MuTect28, SomaticSniper29, and VarScan30,31. To determine if the resulting allele frequency distributions are clinically useful, we analyze the correlation between these distributions and patient survival. Our study demonstrates whether allele frequency variability is clinically predictive and what other genomic features mediate these results. Finally, we discuss implications of a simple evolutionary mechanism on allele frequency distributions using a mathematical modeling approach.


Different mutation callers lead to distinct allele frequency distributions

We analyzed a total of 4722 samples from the TCGA database on a cloud computing platform to explore the effects of mutation calling by MuTect, SomaticSniper, and VarScan on allele frequency distributions and patient survival. Tumor/normal matched BAM files that had been aligned to the hg19 reference were used to call the SNVs (Fig. 1A). The mutation calling pipelines (Fig. S1) were implemented by dockerizing32 each element of the pipeline and linking them through an interface provided by the Cancer Genome Cloud (CGC)33. Three different mutation calling pipelines were run for each tumor/normal pair on Amazon Web Services (AWS)34 through the CGC interface, and the resulting allele frequencies were calculated for each sample.

Figure 1

Analysis design. (A) Schematic of the analysis process for 4722 TCGA samples. Somatic mutation calling was carried out on the NCI Cancer Genomics Cloud33, followed by additional local analysis. (B) Number of samples studied from each cancer.

To analyze the range of possible allele frequency behaviors, we chose 11 cancer types from the TCGA database (Fig. 1B and Fig. S2), namely breast invasive carcinoma (BRCA), colon adenocarcinoma (COAD), glioblastoma multiforme (GBM), head and neck squamous cell carcinoma (HNSC), kidney renal clear cell carcinoma (KIRC), lung adenocarcinoma (LUAD), ovarian serous cystadenocarcinoma (OV), prostate adenocarcinoma (PRAD), skin cutaneous melanoma (SKCM), stomach adenocarcinoma (STAD), and uterine corpus endometrial carcinoma (UCEC).

We found that overall MuTect called the largest number of SNVs and VarScan the least. On average, each sample called by MuTect had 1.4 times more SNVs compared to VarScan and 1.3 times compared to SomaticSniper (Fig. S3). On average, VarScan, SomaticSniper, and MuTect respectively called 1.5, 1.8, and 2.3 times more SNVs compared to the consensus SNVs (i.e. those called by all three mutation callers).

We then compared allele frequency distributions assessed by pairs of mutation callers using the Kolmogorov-Smirnov (KS) test (Fig. 2A,B). Distributions were not very robust across different cancer types (Fig. 2B). SomaticSniper and VarScan produced the most dissimilar allele frequency distributions with 42 ± 14% (mean ± std) of samples being significantly different across cancers. MuTect and VarScan produced the least dissimilar results with 11 ± 8% of samples significantly different. This percentage was 22 ± 14% when MuTect was compared against SomaticSniper. Prostate adenocarcinoma (PRAD), showed unusually robust results, with only 1%, 1%, and 3% of samples being significantly dissimilar when MuTect-SomaticSniper, MuTect-VarScan, and SomaticSniper-VarScan were compared pairwise, respectively.

Figure 2

Comparisons of allele frequency distributions for different mutation callers. (A) Distribution of Kolmogorov-Smirnov (KS) test p-values corresponding to the null hypothesis that mutation callers will produce similar allele frequency distributions, plotted pairwise for HNSC. The red dashed line indicates the Bonferroni corrected significance threshold \(\alpha =0.05\). The percentage of samples that fall below this threshold are shown on each graph. (B) Percentage of significantly different samples for mutation caller pairs, grouped by cancer type. (C) Comparison of allele frequency distributions using earth mover’s distance.

Due to sensitivity of the Kolmogorov-Smirnov test to the number of SNVs in the tumor (Fig. S4), we also used the earth mover’s distance (EMD) to assess differences between allele frequency distributions. EMD produced qualitatively similar results (Fig. 2C) to the Kolmogorov-Smirnov test, with SomaticSniper-VarScan showing the most difference among all pairwise comparisons and MuTect-VarScan showing the least difference. Another method based on cumulative absolute differences between pairs of distributions as well as a non-parametric test based on quadratic differences of distributions35 also yielded similar results (Fig. S5, and Methods). Across all cancers, per-sample correlation coefficient between allele frequencies of shared mutations was 0.97 ± 0.1, regardless of which pair of mutation callers were compared. Hence, differences between mutation caller results tend to be caused by disagreement about mutation calls rather than allele frequencies.

Copy number variations (CNV) can influence allele frequencies and may indirectly shape their distribution. To assess this effect, we repeated the analysis after removing somatic SNVs with copy number aberrations (|CNV| > 0.2). Here and throughout the text we use the CNV quantity to denote \({\mathrm{log}}_{2}(\frac{{\rm{copy}}\,{\rm{number}}}{2})\), as provided by TCGA (see Methods). Comparison of allele frequency distributions using Kolmogorov-Smirnov statistics (Fig. S6) did not produce qualitatively different results from those shown in Fig. 2B, and again showed the most pan-cancer differences between SomaticSniper and VarScan. These results suggest that copy number impacts all mutation callers similarly.

MATH score is a poor predictor of patient survival across cancer types

To investigate the relationship of tumor heterogeneity and survival, Mroz et al.18 introduced a measure of heterogeneity they term MATH. It is the ratio of scaled median absolute deviation (MAD) to median stated in percentage:

$${\rm{MATH}}=100\times \frac{{\rm{MAD}}}{{\rm{Median}}}$$

We calculated this measure for all samples and mutation callers. Overall VarScan yielded higher median MATH score (35.4 ± 5.7) compared to SomaticSniper (24.4 ± 4.8) and MuTect (30.3 ± 5.9) (Fig. S7). Similar to Fig. 2, the MATH scores were also more similar between MuTect and SomaticSniper calls (pan-cancer Spearman correlation coefficient r = 0.7 ± 0.1) and more dissimilar between SomaticSniper and VarScan (r = 0.5 ± 0.2) (Fig. S7).

We then analyzed the relationship between MATH score and patient survival by grouping samples into high or low MATH groups as compared to the median of the cohort. These two groups were then compared using a log-rank test to determine the significance of MATH values on Kaplan-Meier patient survival curves (Fig. 3 and Fig. S8).

Figure 3

Significance analysis of measures of genomic variations and patient survival. (A) Survival analysis log rank test p-values for high and low MATH score groups, and (B) Survival analysis log rank test p-values for high and low CNV standard deviation groups. Stars corresponds to values smaller than significance threshold 0.05. Double stars show significant results after Benjamini-Hochberg correction across all cancer types and mutation callers.

Among the cancers studied, COAD, OV, HNSC, and UCEC showed a significant (p < 0.05) relationship between MATH and survival for at least one caller (e.g. COAD p = 0.07, OV p = 0.02 with SomaticSniper calls). However, only UCEC showed a significant relationship for all three mutation callers (p = 0.00083, 0.0023, 0.011 for MuTect, SomaticSniper, and VarScan calls, respectively). Although these results suggest some clinical predictive power of MATH score, a more conservative approach would be to correct for multiple hypothesis testing. Using the Benjamini-Hochberg correction for all cancers and mutation callers led to significant results only for UCEC, and only when the calls were made by MuTect or SomaticSniper. Therefore the predictive power of MATH score is not robust in a pan-cancer analysis except for possibly UCEC.

Previous studies18,19 have shown a significant relationship between MATH score and patient survival in HNSC. We obtained similar results when the calls were made using MuTect; however the effect was not significant when other callers were used (Fig. S8). Restricting the analysis to the same samples as in19 did not affect the significance of this result (Fig. S9). Thus the clinical predictive power of MATH in HNSC appears to be substantially impacted by the mutation calling method.

To determine the direction of effect of MATH score on survival, we calculated the average survival difference between high and low MATH score groups (see Methods). This analysis indicates that for UCEC higher MATH score is associated with poorer patient survival (Fig. S10). The same trend is observed for COAD and HNSC. For OV, the direction of the trend is caller-dependent.

Copy number mediates prognostic power of allele frequency distributions

Allele frequency variation in a tumor is impacted by locus-to-locus copy number variation in addition to subclonal heterogeneity, and decomposing these two contributions may be important for clinical prognosis. We therefore repeated the above survival analysis but replaced MATH score with the standard deviation of CNV over mutated loci (Fig. 3B and Fig. S11). This CNV analysis yielded more robust results across mutation callers than the MATH score analysis (Fig. S12). Specifically, we found that copy number variation is correlated with survival in KIRC, OV, and UCEC for at least two mutation callers. Multiple hypothesis correction led to a robust effect in UCEC for all mutation callers as well as significance in OV for SomaticSniper and VarScan. This result indicates that copy number variation is a more robust predictor of patient survival than allele frequency distribution.

Despite the lack of statistical significance, for most cancers, higher CNV standard deviation led to poorer survival and this effect was robust across mutation callers (Fig. S10). This was most pronounced for SKCM, STAD, and UCEC. An exception was OV where higher copy number standard deviation was predictive of better survival.

To further distinguish the effect of allele frequencies and copy numbers on patient survival, we filtered out mutant allele frequencies at loci with |CNV| > 0.2 and calculated the log rank test for MATH using the remaining sites (Fig. S13). Analysis of this set with multiple hypothesis correction did not yield any significant results, indicating that MATH clinical predictions are indeed driven by copy number aberrations. This result can be more clearly seen from the correlation between allele frequency variation and copy number variation. Pearson correlation coefficients between copy number standard deviation and MATH score were positive for all tumor types and all mutation callers (Fig. 4A). This effect was even stronger when we compared copy number standard deviation to allele frequency standard deviation (Fig. 4B). This further supports that allele frequency distributions are highly influenced by copy number aberrations across the genome (see examples in Fig. 4C,D).

Figure 4

Correlation between allele frequency variations and copy number variations. (A) Pearson correlation coefficient of CNV standard deviation and MATH score. (B) Pearson correlation coefficient of CNV standard deviation and allele frequency standard deviation. (C) CNV standard deviation versus MATH score, plotted for HNSC (SNVs called by MuTect). Each circle is an individual sample. (D) CNV standard deviation versus allele frequency standard deviation, plotted for HNSC (SNVs called by MuTect).

To explore how the effect of copy number variation on phenotype is confounded by SNVs, we analyzed gene expression in UCEC (Fig. S14 and Methods). The expression levels of most genes (85%, Wilcoxon signed-rank test p = 9e−8) containing both SNVs and copy number amplifications was higher than genes lacking both changes, even after discarding tumor-suppressors and oncogenes (84%, p = 3e−6). However, amplified genes with SNVs were only slightly over-expressed compared to amplified genes without SNVs and this result was not statistically significant (60%, p = 0.38). This suggests that SNVs have a very minor effect on copy number amplification phenotype.

To fully decouple the effects of SNVs and CNVs, we calculated the whole genome CNV standard deviation (WG CNV std) by uniformly sampling the genome for copy number variations and calculating their corresponding standard deviations (see Methods). We found that WG CNV std is highly correlated with CNV std (Spearman correlation 0.93 for UCEC; Fig. S14), indicating an almost uniform distribution of SNVs across the genome. Similar to CNV std, increased WG CNV std also led to better patient survival in OV (log-rank p = 0.0009) and worse patient survival in UCEC (log-rank p = 0.0097), with the former showing significant results after multiple hypothesis correction (see Fig. S14). Overall, these results suggest that SNVs have a minor confounding effect on the clinical prognostic power of global copy number variation.

Distribution-based measures of intratumoral heterogeneity are consistent with many evolutionary scenarios

The multiple contributions to MATH suggest a theoretical question: what is the uniqueness of MATH score in distinguishing different underlying evolutionary scenarios? To answer this we considered the allele frequency distributions in the linear evolution model36 and computed MATH score as a function of model parameters, in the simplifying case of no CNVs. The linear model is the simplest model of tumor evolution with selection and assumes that occasional driver mutations lead to selective sweeps in a background of neutral mutations (Fig. 5A).

Figure 5

Theoretical analysis of MATH score. (A) Schematic diagram of linear tumor evolution model. \({t}_{1}\) is the time from the common ancestor of all tumor cells until the last selective sweep. \({t}_{2}\) is the time from the last selective sweep until biopsy. (B) Contour plots of neutral fraction, \(w\), and MATH as a function of \({t}_{1}\) and \({t}_{2}\) for a noiseless exponentially growing model of linear evolution. \(w\) is the fraction of total SNVs that occurred after the last selective sweep. For this growth model, \(w={2}^{{t}_{2}}/({t}_{1}+{2}^{{t}_{2}})\), where time is measured in cell cycles. (C) MATH score as a function of neutral fraction, \(w\), for a linear tumor evolution model. Dashed lines correspond to analytical calculations. Green dots are samples from the model with 300 SNVs. Red dots are simulated results after incorporation of Gaussian measurement noise. Insets correspond to simulated allele frequency distributions for the two black circles, which have equal MATH scores.

The allele frequency distribution can be specified by a variable w that we call the ‘neutral fraction’ (See Methods, eq. (9)), i.e. the fraction of total somatic mutations that occurred after the last selective sweep. We analytically derived a closed form for MATH score as a function of w (eq. (10)). Assuming exponential growth for time-dependence, there are a continuous set of choices of t1 (the time from the common ancestor of all tumor cells until the last selective sweep) and t2 (the time since the last selective sweep) that lead to identical values of w and MATH (Fig. 5B). Thus MATH score does not uniquely specify a tumor’s evolutionary history, even in the absence of copy number effects.

The model presented above is a simplification of one evolutionary scenario and can be influenced by several factors including mutation rate, proliferation rate and cell death. The derivation of eqs 9 and 10 assumes constant mutation rate per cell division after the last selective sweep, but does not put any restrictions on the form of the growth model, as long as the genotype and phenotype remain uncoupled37. Any global increase in growth rate or decrease in death rate after the last selective sweep is equivalent to an increase in the neutral fraction, w, and does not influence the model otherwise. On the other hand, changes in mutation rates can completely break down these derivations. One exception, however, is if the mutation rate changes during the last selective sweep and remains constant afterwards. An increase of mutation rate in this scenario would not violate model assumptions and is equivalent to an increase in the neutral fraction. Such a scenario may be relevant to some cancer types such as GBM38.

To understand the functional dependence of MATH on neutral fraction, we plotted it against w and compared it to simulations (Fig. 5C). These results show two regimes of behavior across w. MATH score is zero when w ≤ 0.5 (the clonal regime – most mutations are clonal due to the sweep). Addition of measurement noise leads to an increase in MATH score in this clonal regime, but does not significantly affect MATH for w > 0.5 (the neutral regime – most mutations have evolved neutrally but vary in when they arose). In the neutral regime MATH is not a one-to-one function of w, and two very different allele frequency distributions can have the same score. These results show the limitations of single distribution-based scores to uniquely distinguish tumor evolutionary scenarios. Further features of the distribution, such as bimodality, should be used to resolve this degeneracy.


In a pan-cancer analysis of 4722 samples we explored the robustness of allele frequency distributions to mutation calling and their power for clinical prediction. We demonstrated that the mutation calling process can significantly influence the shape of allele frequency distributions. In general, higher variation in allele frequency was correlated with poorer survival, though this result was statistically significant in only a few cases. The only cancer type with statistically significant results robust across mutation callers was UCEC, but this reflected higher levels of copy number variation along the genome rather than increased subclonal heterogeneity. These results suggest that current single-variable measures of subclonal diversity from exome-seq data are not causally related to clinical outcome.

To show the confounding effects of copy number variation on allele frequency distributions, we relied on a crude measure of genome-wide copy number variations (i.e. CNV standard deviation across SNVs), and showed that it is correlated with MATH and is predictive of patient survival in some cases. However, more in-depth analysis of copy number variations is required to fully explore the clinical relevance of CNV burden in tumors. Nevertheless, our results are consistent with copy number aberrations being a more important predictor of outcome, which has previously been reported over pooled TCGA cancer types3. In our analysis most tumor types showed a regular, though not always statistically significant, trend between increased copy number variation and shorter survival time. Notably, high copy number variation has been previously reported to be associated with poor patient survival in serious endometrial carcinoma39. To determine the association between clinical features and CNV standard deviation, we also separately applied clinical feature selection (see Methods) to UCEC, and found that histologic diagnosis is the strongest predictor, with increased CNV variation for serous carcinoma (Fig. S15).

Ovarian cancer is opposite to the common copy number trend, in that tumors with more CNV variation are associated with longer survival. However, in ovarian cancer BRCA1 deletions often lead to the high-CNV tandem duplicator phenotype, and this phenotype has been found to have better clinical outcome40. Indeed, in the TCGA data we observe that increased deletions in BRCA1 are correlated with CNV standard deviation (Fig. S16), suggesting that the ovarian cancer effect is mediated by the tandem duplicator phenotype.

Employing the full spectrum of allele frequency distributions in clinical studies would require multidimensional survival analysis methods, which are sensitive to regression assumptions, or alternatively increasing statistical power by use of larger cohorts. Due to these limitations, in this paper we only focused on reduction of the distribution to a single quantity, namely MATH. Our analysis indicates that allele frequency distributions as quantified by MATH score are not useful clinical prognostic measures across cancer types. However, our work does not rule out the possibility of defining a set of clinically meaningful measures derived from allele frequency distributions. The issue however is that the space of possible measures is dramatically large, and, unless a more mechanism-driven approach is adopted, one would easily encounter underpowered statistics. To reflect this point we explored 11 extra statistics (Fig. S17) and found very little association to patient survival. The only exception was COAD when it was called by SomaticSniper.

A more direct measure of tumor heterogeneity is the cancer cell fraction (CCF), which is the fraction of cells having a specific SNV. We determined the CCFs for all cancers and mutation callers using PyClone7 (see Methods), and calculated MATH score using CCFs instead of allele frequencies (AF). We found that CCF MATH and AF MATH are positively correlated (Fig. S18, mean Pearson correlation coefficient 0.55, with minimum 0.30 for HNSC-SomaticSniper, and maximum 0.82 for GBM-MuTect). Similar to AF MATH, higher CCF MATH was associated to poorer patient survival in UCEC-MuTect, however this result was not robust across mutation callers (Fig. S18).

In addition, we explored the importance of tumor purity on our results. Theoretically, tumor purity scales all mutant allele frequencies by a constant and should not affect MATH score. Order statistics such as KS test would not be affected by purity for a similar reason. However, dependence of mutation-calling errors on allele frequencies, and the removal of allele frequencies smaller than 0.1 in our pipeline are sensitive to purity scaling. To directly assess the effect of tumor purity we therefore compared MATH score against purity scores provided by TCGA, and found very little association between the two (−0.1 < r < 0.1, Fig. S19). Next, we removed samples with purity below 0.8 and compared allele frequency distributions across mutation callers. The results were similar to what we have described in Fig. 2. In the purity filtered datasets, survival analysis of MATH score did not lead to significant results for any cohort. As in the unfiltered analysis, CNV standard deviation was associated with patient survival in UCEC-MuTect and OV-SomaticSniper (Fig. S19).

Overall, we conclude that heterogeneity as quantified by MATH is not a strong predictor of patient survival, whether it is applied to allele frequencies or CCFs. CCF inference is prone to several errors, which can arise from many factors including strong priors in the inference algorithms, errors in allele frequency and copy number measurements, gross underestimation of SNV counts private to small subclones, and subsampling of the tumors. Due to these issues CCF distributions may have unresolved prognostic powers which would require deeper genetic sequencing, use of more informative measures, and an increase in the number of patients and clinical data.

Despite these findings, we cannot conclude that subclonal heterogeneity is irrelevant to survival, as the processes by which resistant populations develop remain poorly understood even though they are crucial to outcome. For example, our work shows that gross estimates of subclonal heterogeneity from exome-seq data have little predictive power, but other studies have shown that resistance can arise from populations too small to be detectable by exome-seq41. Higher resolution measurements of subclonal heterogeneity may solve this challenge, and further development of robust computational analyses will be a critical part of such measurements.

Finally, we have shown that multiple evolutionary histories can lead to the same allele frequency distributions, and that different allele frequency distributions can have the same MATH score. This degeneracy of scenarios leading to the same measurement is an important reason why new descriptors of heterogeneity are needed. Future surveys over different evolutionary scenarios should be valuable for distinguishing what types of heterogeneity measurements are most likely to reveal features predictive of survival.


We studied the robustness of allele frequency distributions to mutation calling procedures across TCGA cancers and explored their prognostic power for patient survival. We found that mutation callers differ significantly in their estimates of the distributions of allele frequencies for individual tumors, and that the association between allele frequency distribution and survival is non-robust to these differences. The major exception is uterine corpus endometrial carcinoma, but the observed effect is mediated by copy number variation rather than subclonal heterogeneity. Our work has implications for cancer precision medicine, as we show that current measures of heterogeneity are not predictive of survival except through an indirect association with copy number variation.


Computational Time

The average time required to run a task was 2 hours and 25 minutes. We ran a total of 14865 jobs, with total wall time of 1496 days.

Sample Selection

Samples were chosen only if tumor/normal Illumina exome-seq data existed with alignment to hg19, and corresponding clinical and Affymetrix SNP Array somatic copy number variation data were present. SNVs were called by three mutation callers and samples were discarded if any mutation caller did not find any somatic SNVs in that sample. If multiple normal samples were available, blood has been preferred over solid tissue. For tumors, primary solid tumor was used if available. The main anomaly was in SKCM, where most TCGA samples are metastatic (Fig. S2).

Mutation Caller Parameters

Mutation calling was done with minor tweaks to the default parameters of each mutation caller (Table 1). For MuTect, these flags control proximal gaps, poor mapping quality, strand bias, clustered positions, mutations in normal sample, low tumor/normal mutation likelihood ratio, and presence in dbsnp. For SomaticSniper we set parameters to ignore loss of heterozygosity and gain of reference. Furthermore SomaticSniper uses a Phred-scaled value, ‘somatic score’, to determine somatic mutations. We have used a high-confidence threshold for this value to improve precision of the algorithm (−Q 40). The parameters for VarScan set minimum for coverage and allele frequency to limit the number of reported mutations. However these parameters will be overridden in the post-processing step.

Table 1 Mutation caller parameters.

Postprocessing Filters

We applied post-processing filters on the output VCF files to extract the somatic SNVs. For MuTect and VarScan we selected SNVs with FILTER = PASS, and in all cases we only used SNVs which had zero allele frequency for normal sample and a non-zero value for the tumor. A read depth filter of minimum 50 was also applied to both normal and tumor samples. Furthermore, we discarded SNVs which had tumor or normal allele frequency \( < 0.1\). For more detail on mutation calling process and parameters see Fig. S1 and Table 1.

Statistical Distances

To calculate the earth mover’s distance (EMD)42, we produced histograms of allele frequencies for each sample using bins of size \(0.025\) and followed the procedure in43 for chain-connected spaces. For two probability distributions \({f}_{1}(x)\) and \({f}_{2}(x)\) with respective normalized histogram abundances \({f}_{\mathrm{1,}j}\) and \({f}_{\mathrm{2,}j}\) at j’th bin (with \(j\le N\)), EMD can be written as43:

$${\rm{EMD}}({f}_{1},{f}_{2})=\sum _{i=1}^{N-1}\sum _{j=1}^{i}|\,{f}_{\mathrm{1,}j}-{f}_{\mathrm{2,}j}|$$

Quantities reported in this paper are the median of this value across each cohort (Fig. 2C).

We also used another method for quantifying differences between distributions of allele frequencies, where we smoothed the histogram of allele frequencies using Gaussian kernel density estimation with standard deviation \(\sigma =0.02\), leading to two continuous functions \({f}_{1}(x)\) and \({f}_{2}(x)\). We then calculated the cumulative absolute difference of these two functions using \({\int }_{0}^{1}|\,{f}_{1}(x)-{f}_{2}(x)|dx\). Again the median of cohort was calculated as a single measure of statistical distance (Fig. S5).

Finally, we also used a non-parametric statistical distance between allele frequency distributions which relies on the average \({L}^{2}\) distance between two distribution functions35. The statistic is defined as \({\int }_{0}^{1}{[{f}_{1}(x)-{f}_{2}(x)]}^{2}dx\), where \({f}_{1}(x)\) and \({f}_{2}(x)\) are the Gaussian kernel density estimations of the two functions (bandwidth = 0.05). We calculated the corresponding p-values by applying a permutation test to each pair of allele frequency sets for which the test statistic was being calculated. This procedure was repeated 100 times and the ratio of tests which were more extreme than the non-permuted test was reported as the p-value.

Allele Frequency and Read Depth

Read depth and allele frequency were extracted from the FORMAT field of VCF files. Multiallelic and biallelic sites were treated similarly and their allele frequencies corresponded to the ratio of alternative alleles to reference alleles. For MuTect and VarScan the allele frequency computed by the software was directly extracted from VCF files, and for SomaticSniper this was done by using the reference and alternative read counts reported by the software.

Copy Number Data

For copy number analysis we used masked copy number level 3 TCGA data measured by Affymetrix SNP Array 6.0 which is readily aligned to hg19 and normalized for somatic copy number detection by removal of frequent germline copy number variations. The quantity used throughout the paper is the Segment Mean column in the ‘nocnv’ files which is either used directly or determined at the SNV locus of interest. This quantity is the average log2 ratio of copy number of the tumor compared to reference (=2) within a segment of the genome where internal changes are minimal. Positive values correspond to amplification and negative values correspond to deletion. Wherever mentioned in the text, copy number filtering was done according to44 where loci with \(|CNV| > 0.2\) were removed.

Survival Data

Survival information was gathered from the TCGA data portal by parsing the clinical json files for field diagnoses.days_to_death as survival time. In cases where this field was not available, we used diagnoses.days_to_last_follow_up instead. The field diagnoses.vital_status was used for determining censored data.

Survival Analysis

Survival analysis was done using Kaplan-Meier curves and log rank test method from the Lifelines Python package45. Only the first 4 years of survival information was used for analyses and any sample with longer overall survival was censored at this time point.

Survival difference values (Fig. S10) were defined by calculating the Kaplan-Meier curves (Figs S8, S11) for two groups with high and low variability score (divided across the median of the score used). We then integrated the absolute value of difference of survival functions:

$$\frac{1}{{T}_{max}}{\int }_{0}^{{T}_{max}}[{S}_{High}(t)-{S}_{Low}(t)]dt$$

where \({S}_{High}(t)\) and \({S}_{Low}(t)\) are the survival functions of the two groups and \({T}_{max}\) corresponds to the maximum time of data collection (4 years). This definition leads to a quantity between \(-\,1\) and \(1\) which is more negative if the high score group has worse survival, and more positive if the high score group has better survival.

Expression Analysis

To determine how copy number amplification influences expression, we downloaded the corresponding RNAseq expression results (RPKM values) of UCEC for each sample from the TCGA database.

For gene \(g\) in patient \(p\), let matrices \({r}_{p,g}\), \({c}_{p,g}\), and \({s}_{p,g}\) respectively be the RPKM value, CNV value, and SNV status (\(1\) if mutated, \(0\) otherwise) of the gene. Furthermore, for total of \(N\) patients let us define \({\mathscr{A}}({x}_{p,g})\) as the average of positive elements of matrix \({x}_{p,g}\) along the columns:

$${\mathscr{A}}({x}_{p,g})\equiv \frac{\sum _{p=1}^{N}{x}_{p,g}}{\sum _{p=1}^{N}u({x}_{p,g})}$$

where \(u(x)=\{\begin{array}{c}0,\,x\le 0,\\ 1,\,x > 0.\end{array}\) is a step function that includes the zero coordinate. The reason for this definition of \({\mathscr{A}}({x}_{p,g})\), is to calculate few different versions of gene expression averages across cohorts based on different criteria illustrated below:

  1. 1.

    mean RPKM (amplified, with SNV):

    $${\mathscr{A}}({r}_{p,g}\times u({c}_{p,g}-{c}_{2}^{th})\times {s}_{p,g})$$
  2. 2.

    mean RPKM (not amplified, without SNV):

    $${\mathscr{A}}({r}_{p,g}\times u({c}_{1}^{th}-{c}_{p,g})\times \mathrm{(1}-{s}_{p,g}))$$
  3. 3.

    mean RPKM (amplified, without SNV):

$${\mathscr{A}}({r}_{p,g}\times u({c}_{p,g}-{c}_{2}^{th})\times \mathrm{(1}-{s}_{p,g}))$$

Here \(\times \) is ordinary element-wise product. \({c}_{1}^{th}=0.1\) and \({c}_{2}^{th}=1.0\) are the CNV thresholds for no amplification and amplification respectively. Note that since amplified SNVs are rare, the averaging in equation (5) could be dropped, rendering this quantity effectively as the single gene RPKM. Furthermore, in cases that the denominator of equation (4) is zero (i.e. no sample meets the criteria), the gene is discarded. Associations between these expression values are reported in Fig. S14.

To determine the effects of tumor suppressors and oncogenes on expression results, we downloaded the list of tumor-suppressor genes from TSGene46,47 and oncogenes from ONGene48 and removed the genes existing in either of the lists.

CNV Standard Deviations

Throughout the text CNV standard deviation (std) of a sample is calculated as the standard deviation of CNVs at all loci that have an SNV.

On the other hand, whole genome (WG) CNV standard deviation is calculated independent of SNVs, by uniform sampling of the genomic regions for which copy number information is available. Equivalently, we can write:

$${\rm{WG}}\,{\rm{CNV}}\,{\rm{std}}=\sqrt{\sum _{i=1}^{N}{p}_{i}{({c}_{i}-\overline{c})}^{2}}$$

where \(\bar{c}=\sum _{i=1}^{N}{p}_{i}{c}_{i}\) is the mean CNV across the genome, \({c}_{i}\) is the CNV of copy number segment i, N is the total number of segments, and \({p}_{i}={l}_{i}/{\sum }_{j=1}^{N}{l}_{j}\) is the fraction of genome covered by segment i with genomic length li.

Mathematical Modeling

The mathematical model presented in this paper is a linear of model of tumor evolution36, where any driver mutation leads to a selective sweep and the remaining mutations are passenger mutations. All the mutations before the last selective sweep are clonal with allele frequency 0.5. The remaining mutations follow the neutral model, with cumulative distribution of allele frequency \(f\) proportional to \(\mathrm{1/}f\)24. Then, the overall allele frequency distribution is the combination of these two distributions sampled according to their occurrence rates (see Supplementary Material):

$$P(F\le f)=\{\begin{array}{cc}0, & f < {f}_{min},\\ \frac{\nu }{2}(\frac{1}{{f}_{min}}-\frac{1}{f}), & {f}_{min}\le f < \,0.5,\\ 1, & f=\mathrm{0.5.}\end{array}$$

where \(\nu =\frac{2w{f}_{min}}{1-2{f}_{min}}\), \(w\) is the ‘neutral fraction’ and is defined as the fraction of all mutations that are neutral, and \({f}_{min}\) is the minimum measurable allele frequency. The latter quantity is necessary in order to avoid singularity at \(f=0\). In our simulations we set \({f}_{min}=0.1\). The results of simulations with no measurement noise (Fig. 5C) were calculated using 300 samples from this distribution, and their variations reflect this sampling error.

We derived a closed form for MATH score of the model as a function of \(w\) (see Supplementary Material for derivation):

$${\rm{M}}{\rm{A}}{\rm{T}}{\rm{H}}=148.26\times \{\begin{array}{cc}0, & w\le \frac{1}{2},\\ \frac{1}{2\varphi }-1, & \frac{1}{2} < w\le \frac{1}{2}+{\rm{\Delta }}w,\\ \frac{\sqrt{{\nu }^{2}+{\varphi }^{2}}-\nu }{\varphi }, & w > \frac{1}{2}+{\rm{\Delta }}w.\end{array}$$

where \({\varphi }=\frac{\nu {f}_{min}}{\nu -{f}_{min}}\), and \({\rm{\Delta }}w=\frac{\sqrt{1+32{f}_{min}^{2}}-1}{16{f}_{min}}\).

The allele frequency measurement error can be modeled by a binomial distribution, where observing a mutation on a sequencing read is a Bernoulli trial. For TCGA whole exome sequencing, read depths are quite large (on average 100×) and this error can be approximated by a Gaussian distribution. Therefore, to implement allele frequency noise we drew 300 samples from the distribution in equation (9) and used each resulting value \(f\) to sample from the normal distribution \({\mathscr{N}}(f,\frac{f\mathrm{(1}-f)}{N})\). Here \(N=100\) is the sequencing read depth.

Cancer Cell Fractions

To determine cancer cell fractions (CCF), we used PyClone7 in the allele-agnostic mode by setting the flag ‘–prior’ to ‘total_copy_number’. For input tsv files, we set normal_cn = 2, minor_cn = 0, and major_cn = round \(\mathrm{(2}\times {2}^{CNV})\), where in the latter equation, CNV is the log2 ratio segmentation information from TCGA SNP Array data. In a few samples a small number of loci had major_cn = 0. We removed these loci from our analysis. Furthermore, to speed up PyClone runtime, if a sample had more than 500 SNVs we randomly removed excess loci.

Alignment to GRCh38

Genomic alignments can lead to different SNVs and/or allele frequencies, depending on read quality and genomic repeats. As a confirmatory step we explored this effect by comparing our results for selected samples against alignments to the new human genome (hg38). To achieve this, we downloaded 227 TCGA breast cancer BAM files of whole exome sequencing data from Cancer Genomics Hub (CGHub)49. After converting the BAM files to FASTQ files, we remapped the FASTQ files to hg38 reference genome with the Burrows-Wheeler Aligner (BWA)50. The somatic SNVs were called by MuTect28. We found that the allele distributions contained less SNVs overall, but their shapes were relatively similar (Fig. S20).

Clinical Feature Selection

Random forest feature selection of clinical data (Fig. S15) was done using ExtraTreesClassifier function from Python package scikit-learn51, with default parameters and 250 estimators. Features with \(\mathrm{20 \% }\) or more unknown values were discarded and the remaining unknown values were set to the median of the feature for numerical features or the mode for categorical features. Data labeling was done by comparing CNV standard deviation to its median.


  1. 1.

    Fisher, R., Pusztai, L. & Swanton, C. Cancer heterogeneity: implications for targeted therapeutics. British journal of cancer 108(3), 479–485 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  2. 2.

    Marusyk, A., Almendro, V. & Polyak, K. Intra-tumour heterogeneity: a looking glass for cancer? Nature Reviews Cancer 12(5), 323–334 (2012).

    Article  PubMed  CAS  Google Scholar 

  3. 3.

    Andor, N. et al. Pan-cancer analysis of the extent and consequences of intratumor heterogeneity. Nature medicine 22(1), 105–113 (2016).

    Article  PubMed  CAS  Google Scholar 

  4. 4.

    Schmitt, M. W., Loeb, L. A. & Salk, J. J. The influence of subclonal resistance mutations on targeted cancer therapy. Nature reviews. Clinical oncology 13(6), 335–347 (2016).

    PubMed  CAS  Google Scholar 

  5. 5.

    Burrell, R. A., McGranahan, N., Bartek, J. & Swanton, C. The causes and consequences of genetic heterogeneity in cancer evolution. Nature 501(7467), 338–345 (2013).

    ADS  Article  PubMed  CAS  Google Scholar 

  6. 6.

    McGranahan, N. & Swanton, C. Biological and therapeutic impact of intratumor heterogeneity in cancer evolution. Cancer cell 27(1), 15–26 (2015).

    Article  PubMed  CAS  Google Scholar 

  7. 7.

    Roth, A. et al. Pyclone: statistical inference of clonal population structure in cancer. Nature methods 11(4), 396–398 (2014).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  8. 8.

    Carter, S. L. et al. Absolute quantification of somatic dna alterations in human cancer. Nature biotechnology 30(5), 413–421 (2012).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. 9.

    Beerenwinkel, N., Schwarz, R. F., Gerstung, M. & Markowetz, F. Cancer evolution: mathematical models and computational inference. Systematic biology 64(1), 1–25 (2015).

    Article  CAS  Google Scholar 

  10. 10.

    Deshwar, A. G. et al. Phylowgs: reconstructing subclonal composition and evolution from whole-genome sequencing of tumors. Genome biology 16(1), 35 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Fischer, A., Vázquez-Garca, I., Illingworth, C. J. & Mustonen, V. High-definition reconstruction of clonal composition in cancer. Cell reports 7(5), 1740–1752 (2014).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  12. 12.

    Donmez, N. et al. Clonality inference from single tumor samples using low coverage sequence data. In: International Conference on Research in Computational Molecular Biology, pp. 83–94, Springer (2016).

  13. 13.

    Nik-Zainal, S. et al. The life history of 21 breast cancers. Cell 149(5), 994–1007 (2012).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  14. 14.

    Farahani, H. et al. Engineered in-vitro cell line mixtures and robust evaluation of computational methods for clonal decomposition and longitudinal dynamics in cancer. Scientific Reports 7(1), 13467 (2017).

    ADS  Article  PubMed  PubMed Central  CAS  Google Scholar 

  15. 15.

    Marusyk, A. & Polyak, K. Tumor heterogeneity: causes and consequences. Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 1805(1), 105–117 (2010).

    Article  CAS  Google Scholar 

  16. 16.

    Jamal-Hanjani, M., Quezada, S. A., Larkin, J. & Swanton, C. Translational implications of tumor heterogeneity. Clinical Cancer Research 21(6), 1258–1266 (2015).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  17. 17.

    Felipe De Sousa, E. M., Vermeulen, L., Fessler, E. & Medema, J. P. Cancer heterogeneitya multifaceted view. EMBO reports 14(8), 686–695 (2013).

    Article  CAS  Google Scholar 

  18. 18.

    Mroz, E. A., Tward, A. M., Hammon, R. J., Ren, Y. & Rocco, J. W. Intra-tumor genetic heterogeneity and mortality in head and neck cancer: Analysis of data from the cancer genome atlas. PLoS Med 12(2), 1–27 (2015).

    Article  CAS  Google Scholar 

  19. 19.

    Morris, L. et al. Pan-cancer analysis of intratumor heterogeneity as a prognostic determinant of survival. Oncotarget 7(9), 10051–10063 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Cai, L., Yuan, W., Zhou Zhang, L. H., Chou, K.-C. In-depth comparison of somatic point mutation callers based on different tumor next-generation sequencing depth data. Scientific reports 6 (2016)

  21. 21.

    Krøigård, A. B., Thomassen, M., Lænkholm, A.-V., Kruse, T. A. & Larsen, M. J. Evaluation of nine somatic variant callers for detection of somatic mutations in exome and targeted deep sequencing data. PloS one 11(3), 0151664 (2016).

    Article  CAS  Google Scholar 

  22. 22.

    Wang, Q. et al. Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers. Genome medicine 5(10), 91 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. 23.

    Xu, H., DiCarlo, J., Satya, R. V., Peng, Q. & Wang, Y. Comparison of somatic mutation calling methods in amplicon and whole exome sequence data. BMC genomics 15(1), 244 (2014).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  24. 24.

    Williams, M. J., Werner, B., Barnes, C. P., Graham, T. A. & Sottoriva, A. Identification of neutral tumor evolution across cancer types. Nature genetics 48(3), 238–244 (2016).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. 25.

    Bozic, I. et al. Accumulation of driver and passenger mutations during tumor progression. Proceedings of the National Academy of Sciences 107(43), 18545–18550 (2010).

    ADS  Article  Google Scholar 

  26. 26.

    Iwasa, Y., Michor, F. & Nowak, M. A. Evolutionary dynamics of escape from biomedical intervention. Proceedings of the Royal Society of London B: Biological Sciences 270(1533), 2573–2578 (2003).

    Article  Google Scholar 

  27. 27.

    Waclaw, B. et al. A spatial model predicts that dispersal and cell turnover limit intratumour heterogeneity. Nature 525(7568), 261–264 (2015).

    ADS  Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. 28.

    Cibulskis, K. et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nature biotechnology 31(3), 213–219 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  29. 29.

    Larson, D. E. et al. Somatic sniper: identification of somatic point mutations in whole genome sequencing data. Bioinformatics 28(3), 311–317 (2012).

    Article  PubMed  CAS  Google Scholar 

  30. 30.

    Koboldt, D. C. et al. Var scan: variant detection in massively parallel sequencing of individual and pooled samples. Bioinformatics 25(17), 2283–2285 (2009).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  31. 31.

    Koboldt, D. C. et al. Var scan2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome research 22(3), 568–576 (2012).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  32. 32.


  33. 33.

    Cancer Genome Cloud.

  34. 34.

    Amazon Web Services.

  35. 35.

    Li, Q. Nonparametric testing of closeness between two unknown distribution functions. Econometric Reviews 15(3), 261–274 (1996).

    ADS  MathSciNet  Article  MATH  Google Scholar 

  36. 36.

    Davis, A., Gao, R. & Navin, N. Tumor evolution: Linear, branching, neutral or punctuated? Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 1867(2), 151–161 (2017).

    Article  CAS  Google Scholar 

  37. 37.

    Noorbakhsh, J. & Chuang, J. H. Uncertainties in tumor allele frequencies limit power to infer evolutionary pressures. Nature genetics 49(9), 1288 (2017).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  38. 38.

    Barthel, F., Wesseling, P., Verhaak, R. Reconstructing the molecular life history of gliomas. bioRxiv, 192369 (2017)

  39. 39.

    Network, C. G. A. R. Integrated genomic characterization of endometrial carcinoma. Nature 497(7447), 67–73 (2013).

    ADS  Article  CAS  Google Scholar 

  40. 40.

    Menghi, F. et al. The tandem duplicator phenotype as a distinct genomic configuration in cancer. Proceedings of the National Academy of Sciences 113(17), 2373–2382 (2016).

    Article  CAS  Google Scholar 

  41. 41.

    Hyo-eun, C. B. et al. Studying clonal dynamics in response to cancer therapy using high-complexity barcoding. Nature medicine 21(5), 440–448 (2015).

    Article  CAS  Google Scholar 

  42. 42.

    Rubner, Y., Tomasi, C. & Guibas, L. J. A metric for distributions with applications to image databases. In: Computer Vision, 1998. Sixth International Conference On, pp. 59–66, IEEE (1998).

  43. 43.

    Martinez, M., Haurilet, M., Al-Halah, Z., Tapaswi, M. & Stiefelhagen, R. Relaxed earth mover’s distances for chain-and tree-connected spaces and their use as a loss function in deep learning. arXiv preprint arXiv:1611.07573 (2016)

  44. 44.

    Laddha, S. V., Ganesan, S., Chan, C. S. & White, E. Mutational landscape of the essential autophagy gene becn1 in human cancers. Molecular cancer research 12(4), 485–490 (2014).

    Article  PubMed  CAS  Google Scholar 

  45. 45.

    C., D.-P. Lifelines.

  46. 46.

    Zhao, M., Sun, J. & Zhao, Z. Tsgene: a web resource for tumor suppressor genes. Nucleic acids research 41(D1), 970–976 (2012).

    Article  CAS  Google Scholar 

  47. 47.

    Zhao, M., Kim, P., Mitra, R., Zhao, J. & Zhao, Z. Tsgene 2.0: an updated literature-based knowledgebase for tumor suppressor genes. Nucleic acids research 44(D1), 1023–1031 (2015).

    Article  CAS  Google Scholar 

  48. 48.

    Liu, Y., Sun, J. & Zhao, M. Ongene: a literature-based database for human oncogenes. Journal of Genetics and Genomics 44(2), 119–121 (2017).

    Article  PubMed  Google Scholar 

  49. 49.

    Wilks, C. et al. The cancer genomics hub (cghub): overcoming cancer through the power of torrential data. Database 2014, 093 (2014).

    Article  CAS  Google Scholar 

  50. 50.

    Li, H. & Durbin, R. Fast and accurate short read alignment with burrows–wheeler transform. Bioinformatics 25(14), 1754–1760 (2009).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  51. 51.

    Pedregosa, F. et al. Scikit-learn: Machine learning in Python. Journal of Machine Learning Research 12, 2825–2830 (2011).

    MathSciNet  MATH  Google Scholar 

Download references


JN would like to thank Joshy George, Francesca Menghi, and Ziming Zhao for helpful comments, Luc Morris for useful discussion and sharing of his previous results, Anna Lisa Lucido for manuscript edits, and Jane Cha for graphics design. JN and SN would like to thank Gaurav Kaushik for instructions on the Cancer Genome Cloud platform. JHC was supported by the National Cancer Institute of the National Institutes of Health under awards [R21CA191848], [R01 CA230031-01] and supplement [R21CA191848-01A1S1]. Research was also partially supported by the National Cancer Institute under award [P30CA034196].

Author information




J.N., H.K., and J.H.C. designed the study. J.N. and J.H.C. wrote the manuscript. J.N. performed computational and statistical analyses. H.K. performed bioinformatics testing. S.N. performed cloud computing setup and pipeline design.

Corresponding author

Correspondence to Jeffrey H. Chuang.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Noorbakhsh, J., Kim, H., Namburi, S. et al. Distribution-based measures of tumor heterogeneity are sensitive to mutation calling and lack strong clinical predictive power. Sci Rep 8, 11445 (2018).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing