scMET Bayesian modelling of DNA methylation heterogeneity at single-cell resolution
Introduction
High throughput measurements of DNA methylomes at single-cell resolution are a promising resource to quantify the heterogeneity of DNA methylation and uncover its role in gene regulation. However, limitations of the technology result in sparse CpG coverage, effectively posing challenges to robustly quantify genuine DNA methylation heterogeneity. Here we introduce scMET, a Bayesian framework for the analysis of single-cell DNA methylation data. This modelling approach combines a hierarchical beta-binomial specification with a generalised linear model framework with the aim of capturing biological overdispersion and overcome data sparsity by sharing information across cells and genomic features.
To disentangle technical from biological variability and overcome data sparsity, scMET couples a hierarchical BB model with a GLM framework (Fig.@ref(fig:scmet)a-b). For each cell i and region j, the input for scMET is the number of CpG sites that are observed to be methylated (Yij) and the total number of sites for which methylation status was recorded (nij). The BB model uses feature-specific mean parameters μj to quantify overall DNAm across all cells and biological overdispersion parameters γj as a proxy for cell-to-cell DNAm heterogeneity. These parameters capture the amount of variability that is not explained by binomial sampling noise, which would only account for technical variation.
The GLM framework is incorporated at two levels. Firstly, to introduce feature-specific covariates xj (e.g. CpG density) that may explain differences in mean methylation μj across features. Secondly, similar to Eling2018, we use a non-linear regression framework to capture the mean-overdispersion trend that is typically observed in high throughput sequencing data, such as scBS-seq (Fig.@ref(fig:scmet)c). This trend is used to derive residual overdispersion parameters ϵj — a measure of cell-to-cell variability that is not confounded by mean methylation. Feature-specific parameters are subsequently used for: (i) feature selection, to identify highly variable features (HVFs) that drive cell-to-cell epigenetic heterogeneity (Fig.@ref(fig:scmet)d) and (ii) differential methylation testing, to highlight features that show differences in DNAm mean or variability between specified groups of cells (Fig.@ref(fig:scmet)e).
scMET model overview.
Installation
scMET analysis on synthetic data
To highlight the main functionality of scMET we first
apply it on synthetic data, where we can assess the accuracy of the
inferred parameters (μ and
γ) as well as compare it with
the maximum likelihood estimation of simple beta-binomial (BB-MLE)
model.
# Load package
suppressPackageStartupMessages(library(scMET))
suppressPackageStartupMessages(library(data.table))
set.seed(123)Loading synthetic data
scMET comes with simulated scBS-seq data from a single population.
The users can generate their own synthetic data using the
scmet_simulate function. NOTE For
interoperability of scMET and SingleCellExperiment objects
see last section of this vignette.
## [1] "Y" "X" "theta_true"
## [4] "theta_priors_true" "opts"Here, Y is a data.table containing the
scBS-seq data in long format, where total_reads corresponds
to the total number of covered CpGs nij and
met_reads to number of methylated CpGs Yij in
cell i and feature j (see Fig.@ref(fig:scmet)). This is
the data format that scMET requires as input.
## Feature Cell total_reads met_reads
## <char> <char> <int> <num>
## 1: Feature_1 Cell_13 14 9
## 2: Feature_1 Cell_21 9 9
## 3: Feature_1 Cell_11 10 8
## 4: Feature_1 Cell_50 10 1
## 5: Feature_1 Cell_44 11 6
## 6: Feature_1 Cell_14 12 8Next, X is a matrix containing the feature-specific
covariates that might explain differences in mean methylation. The first
column of X is the bias term and contains a vector of 1s. This is an
optional input when performing inference using
scMET.
## intercept cpg_density
## Feature_1 1 -0.77132814
## Feature_10 1 0.30623073
## Feature_100 1 -1.46447533
## Feature_101 1 -1.05901022
## Feature_102 1 0.96694264
## Feature_103 1 0.06700105The theta_true element just contains the true μ and γ parameters used to generate the
scBS-seq data Y. We will use these to assess our prediction
performance later. Finally the theta_priors_true contains
the prior hyper-parameters which we defined to generate the synthetic
data (top level parameters in Fig.@ref(fig:scmet)).
## mu gamma
## Feature_1 0.6201633 0.2953617
## Feature_10 0.3066003 0.3630327
## Feature_100 0.8417903 0.1483870
## Feature_101 0.9307007 0.1619025
## Feature_102 0.1089840 0.2645526
## Feature_103 0.4856963 0.3154443## $w_mu
## [1] -0.5 -1.5
##
## $w_gamma
## [1] -1.2 -0.3 1.1 -0.9
##
## $s_mu
## [1] 1
##
## $s_gamma
## [1] 0.2Now let’s visualise how the mean-overdispersion trend looks like in
our synthetic data and also the association between mean methylation and
covariates X, which here we will assume is CpG density.
par(mfrow = c(1,2))
plot(scmet_dt$theta_true$mu, scmet_dt$theta_true$gamma, pch = 20,
xlab = expression(paste("Mean methylation ", mu)),
ylab = expression(paste("Overdsispersion ", gamma)))
plot(scmet_dt$X[,2], scmet_dt$theta_true$mu, pch = 20,
xlab = "X: CpG density",
ylab = expression(paste("Mean methylation ", mu)))
scMET inference
Now we can perform inference on the simulated data using the
scmet function. In addition to providing the input data
Y and covariates X, we set L = 4
radial basis functions to model the mean-overdispersion relationship.
Also, we set the total number of VB iterations to
iter = 500 for efficiency purposes (hence the model will
most probably not converge and which can be seen by the fitted lines
being further away than expected). We let all the other parameters as
default.
NOTE 1 The user should set this to a much higher value, e.g. around 20,000 when running VB so the model converges.
NOTE 2 For relatively small datasets we recommend
using the MCMC implementation of scMET, i.e. setting
use_mcmc = TRUE, since it is more stable than the VB
approximation and gives more accurate results.
# Run with seed for reproducibility
fit_obj <- scmet(Y = scmet_dt$Y, X = scmet_dt$X, L = 4,
iter = 1000, seed = 12)## Chain 1: ------------------------------------------------------------
## Chain 1: EXPERIMENTAL ALGORITHM:
## Chain 1: This procedure has not been thoroughly tested and may be unstable
## Chain 1: or buggy. The interface is subject to change.
## Chain 1: ------------------------------------------------------------
## Chain 1:
## Chain 1:
## Chain 1:
## Chain 1: Gradient evaluation took 0.000866 seconds
## Chain 1: 1000 transitions using 10 leapfrog steps per transition would take 8.66 seconds.
## Chain 1: Adjust your expectations accordingly!
## Chain 1:
## Chain 1:
## Chain 1: Begin eta adaptation.
## Chain 1: Iteration: 1 / 250 [ 0%] (Adaptation)
## Chain 1: Iteration: 50 / 250 [ 20%] (Adaptation)
## Chain 1: Iteration: 100 / 250 [ 40%] (Adaptation)
## Chain 1: Iteration: 150 / 250 [ 60%] (Adaptation)
## Chain 1: Iteration: 200 / 250 [ 80%] (Adaptation)
## Chain 1: Success! Found best value [eta = 1] earlier than expected.
## Chain 1:
## Chain 1: Begin stochastic gradient ascent.
## Chain 1: iter ELBO delta_ELBO_mean delta_ELBO_med notes
## Chain 1: 100 -8816.455 1.000 1.000
## Chain 1: 200 -8185.937 0.539 1.000
## Chain 1: 300 -8119.809 0.043 0.077
## Chain 1: 400 -8024.891 0.010 0.012
## Chain 1: 500 -8012.193 0.007 0.012
## Chain 1: 600 -7966.628 0.004 0.006
## Chain 1: 700 -7987.344 0.004 0.006
## Chain 1: 800 -7972.263 0.002 0.003
## Chain 1: 900 -7952.611 0.002 0.002
## Chain 1: 1000 -7997.019 0.004 0.006
## Chain 1: Informational Message: The maximum number of iterations is reached! The algorithm may not have converged.
## Chain 1: This variational approximation is not guaranteed to be meaningful.
## Chain 1:
## Chain 1: Drawing a sample of size 2000 from the approximate posterior...
## Chain 1: COMPLETED.Output summary
The scmet returns a scmet_<mode>
object (mode either vb or mcmc) with the
following structure:
## [1] "scmet_vb"## [1] "posterior" "Y" "X" "feature_names"
## [5] "theta_priors" "opts"Here the most important entry is the posterior entry,
which is a list containing the posterior draws for each of the model
parameters. All other elements contain the input data and initialised
hyper-parameter values for reproducibility purposes.
## [1] "mu" "gamma" "epsilon" "w_mu" "w_gamma" "s_gamma" "lp__"# Rows correspond to draws and columns to parameter dimensions
# here number of features.
dim(fit_obj$posterior$mu)## [1] 2000 150##
## iterations Feature_1 Feature_10 Feature_100
## [1,] 0.580 0.289 0.686
## [2,] 0.514 0.347 0.767
## [3,] 0.615 0.302 0.749
## [4,] 0.514 0.409 0.834
## [5,] 0.501 0.265 0.749##
## iterations Feature_1 Feature_10 Feature_100
## [1,] 0.315 0.372 0.359
## [2,] 0.288 0.410 0.201
## [3,] 0.110 0.130 0.141
## [4,] 0.114 0.408 0.247
## [5,] 0.216 0.179 0.208# First 5 draws for covariate coefficients
# number of columns equal to ncol(X) = 2
fit_obj$posterior$w_mu[1:5, ]##
## iterations intercept cpg_density
## [1,] -0.482 -1.536
## [2,] -0.419 -1.836
## [3,] -0.303 -1.739
## [4,] -0.702 -1.745
## [5,] -0.359 -1.790# First 5 draws for RBF coefficients
# number of columns equal to L = 4
fit_obj$posterior$w_gamma[1:5, ]##
## iterations rbf1 rbf2 rbf3 rbf4
## [1,] -1.727 0.734 0.858 0.132
## [2,] -1.824 0.770 0.995 0.103
## [3,] -1.841 0.884 0.966 0.031
## [4,] -1.805 0.812 1.028 0.348
## [5,] -1.857 0.714 0.930 -0.009Plotting mean-overdispersion relationship
Next we plot the posterior median parameter estimates of μ and γ together with the fitted non-linear trend. The color code is used to represent areas with high (green and yellow) and low (blue) concentration of features via kernel density estimation. Mostly useful when visualising datasets with large number of features.
gg1 <- scmet_plot_mean_var(obj = fit_obj, y = "gamma",
task = NULL, show_fit = TRUE)
gg2 <- scmet_plot_mean_var(obj = fit_obj, y = "epsilon",
task = NULL, show_fit = TRUE)
cowplot::plot_grid(gg1, gg2, ncol = 2)
As expected we observe no association between the mean - residual overdisperion relatioship.
Comparing true versus estimated parameters
Next we assess the predictive performance of scMET by comparing the posterior estimates with the true parameter values used to generate the synthetic data.
# Mean methylation estimates
gg1 <- scmet_plot_estimated_vs_true(obj = fit_obj, sim_dt = scmet_dt,
param = "mu")
# Overdispersion estimates
gg2 <- scmet_plot_estimated_vs_true(obj = fit_obj, sim_dt = scmet_dt,
param = "gamma")
cowplot::plot_grid(gg1, gg2, ncol = 2)
scMET versus beta-binomial MLE (shrinkage)
Below we assess the predictive performance of scMET compared to the maximum likelihood estimates from a beta-binomial model. First we obtain MLE estimates:
# Obtain MLE estimates by calling the bb_mle function
bbmle_fit <- scmet_dt$Y[, bb_mle(cbind(total_reads, met_reads)),
by = c("Feature")]
bbmle_fit <- bbmle_fit[, c("Feature", "mu", "gamma")]
head(bbmle_fit)## Feature mu gamma
## <char> <num> <num>
## 1: Feature_1 0.62682041 1.800892e-01
## 2: Feature_10 0.25923353 2.530192e-01
## 3: Feature_100 0.83186860 2.486058e-01
## 4: Feature_101 0.95475109 1.184721e-06
## 5: Feature_102 0.08642232 1.352157e-01
## 6: Feature_103 0.47120018 2.669786e-01As we can see, scMET can more accurately estimate the overdispersion parameter γ by shrinking the MLE estimates towards to population average, resulting in more robust estimates.
# Overdispersion estimates MLE vs scMET
# subset of features to avoid over-plotting
scmet_plot_estimated_vs_true(obj = fit_obj, sim_dt = scmet_dt,
param = "gamma", mle_fit = bbmle_fit)
The above sections mostly focused on assessing the prediction performance of scMET. Below we show how the user can use scMET for downstream analyses, such as feature selection and differential methylation testing.
Identifying highly variable features
After fitting the scMET model, we now show how to perform feature selection; that is to identify highly variable features (HVF) which potentially drive cell-to-cell DNA methylation heterogeneity. We will identify HVFs based on the residual overdispersion estimates ϵ (This is the default and recommended approach of scMET. The user can also perform HVF analysis based on the overdispersion parameter γ, which however will be confounded by the mean methylation levels).
We can perform HVF analysis simply by calling the
scmet_hvf function. This will create a new list named
hvf within the fit_obj object.
# Run HVF analysis
fit_obj <- scmet_hvf(scmet_obj = fit_obj, delta_e = 0.75,
evidence_thresh = 0.8, efdr = 0.1)## 6 Features classified as highly variable using:
## - The 75 percentile of variable genes
## - Evidence threshold = 0.80275
## - EFDR = 10.3%
## - EFNR = 25.8%## feature_name mu gamma epsilon tail_prob is_variable
## Feature_8 Feature_8 0.075 0.3800 0.543 0.9760 TRUE
## Feature_112 Feature_112 0.149 0.5340 0.924 0.9740 TRUE
## Feature_146 Feature_146 0.028 0.3235 0.460 0.9470 TRUE
## Feature_128 Feature_128 0.091 0.3460 0.339 0.8565 TRUE
## Feature_49 Feature_49 0.385 0.4855 0.224 0.8200 TRUE
## Feature_136 Feature_136 0.162 0.3745 0.238 0.8085 TRUEHere the tail_prob column denotes the evidence our model
provides of a feature being called as HVF (the higher the larger the
evidence), and the is_variable column denotes the output
whether the feature was called as HVF or not.
Below we show the grid search to obtain the optimal posterior evidence threshold to achieve EFDR = 10%.
Next we can also plot the corresponding tail posterior probabilities as a function of μ and plot the mean - overdispersion relationship coloured by the HVF analysis.
gg1 <- scmet_plot_vf_tail_prob(obj = fit_obj, x = "mu", task = "hvf")
gg2 <- scmet_plot_mean_var(obj = fit_obj, y = "gamma", task = "hvf")
cowplot::plot_grid(gg1, gg2, ncol = 2)
NOTE One could perform the exact analysis for identifying lowly variable features (LVFs), although in general these are less useful for downstream analysis, such as clustering, since they denote regulatory regions that have stable DNAm patterns across cells.
Differential analysis with scMET
scMET has additional functionality for calling differentially methylated (DM) and differentially variable (DV) features when analysing cells from two conditions/populations.
To perform differential testing, scMET contains simulated data from
two conditions/groups of cells, where a subset of features are DM and
some others are DV between groups A and
B. The user can generate their own synthetic data using
the scmet_simulate_diff function. Below we show the
structure of the scmet_diff_dt object.
## [1] "scmet_dt_A" "scmet_dt_B"
## [3] "opts" "diff_var_features"
## [5] "diff_var_features_up" "diff_var_features_down"
## [7] "diff_mean_features" "diff_mean_features_up"
## [9] "diff_mean_features_down"Below we plot the mean-overdispersion relationship of the true parameters for each group, and highlight with red colour the features that are truly differentially variable in group B compared to group A.
# Extract DV features
dv <- scmet_diff_dt$diff_var_features$feature_idx
# Parameters for each group
theta_A <- scmet_diff_dt$scmet_dt_A$theta_true
theta_B <- scmet_diff_dt$scmet_dt_B$theta_true
par(mfrow = c(1,2))
# Group A mean - overdispersion relationship
plot(theta_A$mu, theta_A$gamma, pch = 20, main = "Group A",
xlab = expression(paste("Mean methylation ", mu)),
ylab = expression(paste("Overdsispersion ", gamma)))
points(theta_A$mu[dv], theta_A$gamma[dv], col = "red", pch = 20)
# Group B mean - overdispersion relationship
plot(theta_B$mu, theta_B$gamma, pch = 20, main = "Group B",
xlab = expression(paste("Mean methylation ", mu)),
ylab = expression(paste("Overdsispersion ", gamma)))
points(theta_B$mu[dv], theta_B$gamma[dv], col = "red", pch = 20)
The scmet_dt_A and scmet_dt_B are the two
simulated datasets, having the same structure as the
scmet_dt object in the above sections. The additional
elements contain information about which features are DM or DV across
populations.
Fitting scMET for each group
To perform differential analysis, we first need to run the
scmet function on each dataset/group independently.
NOTE 1 The user should set this to a much higher value, e.g. around 20,000 when running VB.
NOTE 2 For relatively small datasets we recommend
using the MCMC implementation of scMET, i.e. setting
use_mcmc = TRUE, since it is more stable than the VB
approximation and generally gives more accurate results.
# Run scMET for group A
fit_A <- scmet(Y = scmet_diff_dt$scmet_dt_A$Y,
X = scmet_diff_dt$scmet_dt_A$X, L = 4,
iter = 300, seed = 12)## Chain 1: ------------------------------------------------------------
## Chain 1: EXPERIMENTAL ALGORITHM:
## Chain 1: This procedure has not been thoroughly tested and may be unstable
## Chain 1: or buggy. The interface is subject to change.
## Chain 1: ------------------------------------------------------------
## Chain 1:
## Chain 1:
## Chain 1:
## Chain 1: Gradient evaluation took 0.001864 seconds
## Chain 1: 1000 transitions using 10 leapfrog steps per transition would take 18.64 seconds.
## Chain 1: Adjust your expectations accordingly!
## Chain 1:
## Chain 1:
## Chain 1: Begin eta adaptation.
## Chain 1: Iteration: 1 / 250 [ 0%] (Adaptation)
## Chain 1: Iteration: 50 / 250 [ 20%] (Adaptation)
## Chain 1: Iteration: 100 / 250 [ 40%] (Adaptation)
## Chain 1: Iteration: 150 / 250 [ 60%] (Adaptation)
## Chain 1: Iteration: 200 / 250 [ 80%] (Adaptation)
## Chain 1: Success! Found best value [eta = 1] earlier than expected.
## Chain 1:
## Chain 1: Begin stochastic gradient ascent.
## Chain 1: iter ELBO delta_ELBO_mean delta_ELBO_med notes
## Chain 1: 100 -25145.285 1.000 1.000
## Chain 1: 200 -22617.738 0.556 1.000
## Chain 1: 300 -22382.208 0.061 0.112
## Chain 1: Informational Message: The maximum number of iterations is reached! The algorithm may not have converged.
## Chain 1: This variational approximation is not guaranteed to be meaningful.
## Chain 1:
## Chain 1: Drawing a sample of size 2000 from the approximate posterior...
## Chain 1: COMPLETED.# Run scMET for group B
fit_B <- scmet(Y = scmet_diff_dt$scmet_dt_B$Y,
X = scmet_diff_dt$scmet_dt_B$X, L = 4,
iter = 300, seed = 12)## Chain 1: ------------------------------------------------------------
## Chain 1: EXPERIMENTAL ALGORITHM:
## Chain 1: This procedure has not been thoroughly tested and may be unstable
## Chain 1: or buggy. The interface is subject to change.
## Chain 1: ------------------------------------------------------------
## Chain 1:
## Chain 1:
## Chain 1:
## Chain 1: Gradient evaluation took 0.001818 seconds
## Chain 1: 1000 transitions using 10 leapfrog steps per transition would take 18.18 seconds.
## Chain 1: Adjust your expectations accordingly!
## Chain 1:
## Chain 1:
## Chain 1: Begin eta adaptation.
## Chain 1: Iteration: 1 / 250 [ 0%] (Adaptation)
## Chain 1: Iteration: 50 / 250 [ 20%] (Adaptation)
## Chain 1: Iteration: 100 / 250 [ 40%] (Adaptation)
## Chain 1: Iteration: 150 / 250 [ 60%] (Adaptation)
## Chain 1: Iteration: 200 / 250 [ 80%] (Adaptation)
## Chain 1: Success! Found best value [eta = 1] earlier than expected.
## Chain 1:
## Chain 1: Begin stochastic gradient ascent.
## Chain 1: iter ELBO delta_ELBO_mean delta_ELBO_med notes
## Chain 1: 100 -24710.879 1.000 1.000
## Chain 1: 200 -22169.801 0.557 1.000
## Chain 1: 300 -21916.277 0.063 0.115
## Chain 1: Informational Message: The maximum number of iterations is reached! The algorithm may not have converged.
## Chain 1: This variational approximation is not guaranteed to be meaningful.
## Chain 1:
## Chain 1: Drawing a sample of size 2000 from the approximate posterior...
## Chain 1: COMPLETED.Showing mean - overdispersion plots for each group
gg1 <- scmet_plot_mean_var(obj = fit_A, y = "gamma", task = NULL,
title = "Group A")
gg2 <- scmet_plot_mean_var(obj = fit_B, y = "gamma", task = NULL,
title = "Group B")
cowplot::plot_grid(gg1, gg2, ncol = 2)
Running differential analysis
Now we can perform the DM and DV analysis by calling the
scmet_differential function. NOTE that
only those features that are common across the two groups will be kept
for this analysis.
# Run differential analysis with small evidence_thresh
# tp obtain more hits.
diff_obj <- scmet_differential(obj_A = fit_A, obj_B = fit_B,
evidence_thresh_m = 0.65,
evidence_thresh_e = 0.65,
group_label_A = "A",
group_label_B = "B")## For Differential mean task:
## Not possible to find evidence probability threshold (>0.6)
## that achieves desired EFDR level (tolerance +- 0.025)
## Output based on the closest possible value.## For Differential overdispersion task:
## Evidence probability threshold chosen via EFDR valibration is too low.
## Probability threshold set automatically equal to 'evidence_thresh_g'.## ---------------------------------------
## The user excluded 0 features.
## These features are marked as 'ExcludedByUser'
## and are excluded from EFDR calibration.## -------------------------------------------------------------
## 41 features with a change in mean methylation:
## - Higher methylation in A samples: 15
## - Higher methylation in B samples: 26
## - Odds ratio tolerance = 1.5
## - Probability evidence threshold=0.72225
## - EFDR = 1.25%
## - EFNR = 2.1%.
## -------------------------------------------------------------
##
## -------------------------------------------------------------
## 56 features with a change in over-dispersion:
## - Higher dispersion in A samples: 27
## - Higher dispersion in B samples: 29
## - Odds ratio tolerance = 1.5
## - Probability evidence threshold=0.8
## - EFDR = 1.77%
## - EFNR = 7.81%
## NOTE: differential dispersion assessment only applied to the
## 159 features for which the mean did not change
## and that were included for testing.
## --------------------------------------------------------------
## -------------------------------------------------------------
## 99 features with a change in residual over dispersion:
## - Higher residual dispersion in A samples: 75
## - Higher residual dispersion in B samples: 24
## - Odds ratio tolerance = 1.5
## - Probability evidence threshold=0.662
## - EFDR = 5%
## - EFNR = 14.09%.
## --------------------------------------------------------------NOTE sometimes the method returns a message that it could not obtain an acceptable evidence threshold to achieve EFDR = 5%. Then by by default the evidence threshold is set to the initial value. This does not mean though that the test failed.
The diff_obj stores all the differential analysis
information in the following structure:
## [1] "scmet_differential"## [1] "diff_mu_summary" "diff_epsilon_summary" "diff_gamma_summary"
## [4] "diff_mu_thresh" "diff_epsilon_thresh" "diff_gamma_thresh"
## [7] "opts"The diff_<mode>_summary entries contain the
summary of the differential analysis, whereas the
diff_<mode>_thresh slots contain information about
the optimal posterior evidence threshold search to achieve the required
EFDR.
## feature_name mu_overall mu_A mu_B mu_LOR mu_OR
## Feature_1 Feature_1 0.12300 0.1830 0.063 1.1946932 3.3025444
## Feature_116 Feature_116 0.30650 0.2020 0.411 -1.0119451 0.3635112
## Feature_12 Feature_12 0.78300 0.7260 0.840 -0.6862328 0.5034692
## Feature_125 Feature_125 0.20200 0.2480 0.156 0.5798989 1.7858579
## Feature_128 Feature_128 0.32275 0.3765 0.269 0.4960116 1.6421586
## Feature_134 Feature_134 0.12850 0.0930 0.164 -0.6442583 0.5250518
## mu_tail_prob mu_diff_test
## Feature_1 1 A+
## Feature_116 1 B+
## Feature_12 1 B+
## Feature_125 1 A+
## Feature_128 1 A+
## Feature_134 1 B+## mu_diff_test n
## 1 A+ 15
## 2 B+ 26
## 3 NoDiff 159## feature_name epsilon_overall epsilon_A epsilon_B epsilon_change
## Feature_1 Feature_1 0.41025 0.7045 0.1160 0.585
## Feature_115 Feature_115 1.00700 0.5495 1.4645 -0.919
## Feature_12 Feature_12 -0.11650 0.5205 -0.7535 1.276
## Feature_122 Feature_122 0.41250 0.8870 -0.0620 0.952
## Feature_124 Feature_124 -0.13400 0.3200 -0.5880 0.913
## Feature_125 Feature_125 -0.58450 -0.0700 -1.0990 1.026
## epsilon_tail_prob epsilon_diff_test mu_overall mu_A mu_B
## Feature_1 1 A+ 0.1230 0.183 0.063
## Feature_115 1 B+ 0.3745 0.350 0.399
## Feature_12 1 A+ 0.7830 0.726 0.840
## Feature_122 1 A+ 0.4875 0.522 0.453
## Feature_124 1 A+ 0.7765 0.751 0.802
## Feature_125 1 A+ 0.2020 0.248 0.156## epsilon_diff_test n
## 1 A+ 75
## 2 B+ 24
## 3 NoDiff 101Let us plot first the grid search for optimal evidence threshold.
gg1 <- scmet_plot_efdr_efnr_grid(obj = diff_obj, task = "diff_mu")
gg2 <- scmet_plot_efdr_efnr_grid(obj = diff_obj, task = "diff_epsilon")
cowplot::plot_grid(gg1, gg2, ncol = 2)
Plotting differential hits
Below we show volcano plots for DM and DV analysis. Red and green colours correspond to features that are more methylated or variable in group A and group B, respectively.
Below we show MA plots for DM and DV analysis.
# MA plot for DM analysis and x axis overall mean methylation
gg1 <- scmet_plot_ma(diff_obj, task = "diff_mu", x = "mu")
# MA plot for DV analysis and x axis overall mean methylation
gg2 <- scmet_plot_ma(diff_obj, task = "diff_epsilon", x = "mu")
cowplot::plot_grid(gg1, gg2, ncol = 2)
Interoperability between scMET and the SingleCellExperiment class
In this section we show the ability to convert between scMET objects
and SingleCellExperiment (SCE) objects.
SingleCellExperiment is a class for storing single-cell
experiment data used by many Bioconductor analysis packages. To the best
of our knowledge there is no standard format for storing scBS-seq data.
However, to ease analysis pipeline with scMET for users with experience
in Bioconductor we provide helper functions for converting between those
formats.
The structure of the SCE object to store scBS-seq data is as follows.
We create two assays, met storing methylated CpGs and
total storing total number of CpGs. Rows correspond to
features and columns to cells, similar to scRNA-seq convention. To
distinguish between a feature (in a cell) having zero methylated CpGs vs
not having CpG coverage at all (missing value), we check if the
corresponding entry in total is zero as well. Next
rownames and colnames should store the feature
and cell names, respectively. Covariates X that might
explain variability in mean (methylation) should be stored in
metadata(rowData(sce))$X.
Below we show an example of converting between these formats.
## Feature Cell total_reads met_reads
## <char> <char> <int> <num>
## 1: Feature_1 Cell_13 14 9
## 2: Feature_1 Cell_21 9 9
## 3: Feature_1 Cell_11 10 8
## 4: Feature_1 Cell_50 10 1
## 5: Feature_1 Cell_44 11 6
## 6: Feature_1 Cell_14 12 8Convert from scMET to SCE object:
# We could set X = NULL if we do not have covariates
Y_sce <- scmet_to_sce(Y = Y_scmet, X = X)
Y_sce## class: SingleCellExperiment
## dim: 150 50
## metadata(0):
## assays(2): met total
## rownames(150): Feature_1 Feature_10 ... Feature_98 Feature_99
## rowData names(1): feature_names
## colnames(50): Cell_13 Cell_21 ... Cell_5 Cell_36
## colData names(0):
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):Next, we convert back to scMET object:
## Feature Cell total_reads met_reads
## <fctr> <fctr> <num> <num>
## 1: Feature_1 Cell_13 14 9
## 2: Feature_1 Cell_21 9 9
## 3: Feature_1 Cell_11 10 8
## 4: Feature_1 Cell_50 10 1
## 5: Feature_1 Cell_44 11 6
## 6: Feature_1 Cell_14 12 8Finally we can check that the final object is the same as our initial one:
## [1] TRUESession Info
This vignette was compiled using:
## R version 4.4.2 (2024-10-31)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.1 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
## LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.26.so; LAPACK version 3.12.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Etc/UTC
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] data.table_1.16.2 scMET_1.9.0 knitr_1.49 BiocStyle_2.35.0
##
## loaded via a namespace (and not attached):
## [1] tidyselect_1.2.1 viridisLite_0.4.2
## [3] dplyr_1.1.4 farver_2.1.2
## [5] loo_2.8.0 viridis_0.6.5
## [7] fastmap_1.2.0 SingleCellExperiment_1.29.1
## [9] digest_0.6.37 lifecycle_1.0.4
## [11] StanHeaders_2.32.10 magrittr_2.0.3
## [13] compiler_4.4.2 rlang_1.1.4
## [15] sass_0.4.9 tools_4.4.2
## [17] utf8_1.2.4 yaml_2.3.10
## [19] S4Arrays_1.7.1 labeling_0.4.3
## [21] pkgbuild_1.4.5 curl_6.0.1
## [23] DelayedArray_0.33.2 abind_1.4-8
## [25] withr_3.0.2 BiocGenerics_0.53.3
## [27] sys_3.4.3 grid_4.4.2
## [29] stats4_4.4.2 fansi_1.0.6
## [31] colorspace_2.1-1 inline_0.3.20
## [33] ggplot2_3.5.1 scales_1.3.0
## [35] MASS_7.3-61 SummarizedExperiment_1.37.0
## [37] cli_3.6.3 rmarkdown_2.29
## [39] crayon_1.5.3 generics_0.1.3
## [41] RcppParallel_5.1.9 httr_1.4.7
## [43] cachem_1.1.0 rstan_2.32.6
## [45] zlibbioc_1.52.0 splines_4.4.2
## [47] assertthat_0.2.1 parallel_4.4.2
## [49] BiocManager_1.30.25 XVector_0.47.0
## [51] matrixStats_1.4.1 vctrs_0.6.5
## [53] V8_6.0.0 Matrix_1.7-1
## [55] jsonlite_1.8.9 VGAM_1.1-12
## [57] IRanges_2.41.1 S4Vectors_0.45.2
## [59] maketools_1.3.1 jquerylib_0.1.4
## [61] glue_1.8.0 codetools_0.2-20
## [63] cowplot_1.1.3 gtable_0.3.6
## [65] GenomeInfoDb_1.43.2 QuickJSR_1.4.0
## [67] GenomicRanges_1.59.1 UCSC.utils_1.3.0
## [69] munsell_0.5.1 tibble_3.2.1
## [71] pillar_1.9.0 htmltools_0.5.8.1
## [73] logitnorm_0.8.39 GenomeInfoDbData_1.2.13
## [75] R6_2.5.1 evaluate_1.0.1
## [77] lattice_0.22-6 Biobase_2.67.0
## [79] bslib_0.8.0 rstantools_2.4.0
## [81] Rcpp_1.0.13-1 coda_0.19-4.1
## [83] gridExtra_2.3 SparseArray_1.7.2
## [85] xfun_0.49 MatrixGenerics_1.19.0
## [87] buildtools_1.0.0 pkgconfig_2.0.3Acknowledgements
This study was supported by funding from the University of Edinburgh and Medical Research Council (core grant to the MRC Institute of Genetics and Cancer). Many thanks to John Riddell for the conversion functions.