In the previous vignette “Introduction to coMethDMR”, we discussed components of the coMethDMR pipeline and presented example R scripts for running an analysis with coMethDMR serially. However, because identifying co-methylated clusters and fitting mixed effects models on large numbers of genomic regions can be computationally expensive, we illustrate implementation of parallel computing for coMethDMR via the BiocParallel R package in this vignette.
The latest version can be installed by:
if (!requireNamespace("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("coMethDMR")First, we load these two packages.
In Section 2, we give a brief re-introduction to the example data. In Section 3, we present example scripts for analyzing a single type (e.g. genic regions) of genomic regions using parallel computing. In Section 4, we present example scripts for analyzing genic and intergenic regions on the Illumina arrays using parallel computing.
For illustration, we use a subset of prefrontal cortex methylation data (GEO GSE59685) described in Lunnon et al. (2014). This example dataset includes beta values for 8552 CpGs on chromosome 22 for a random selection of 20 subjects.
We assume quality control and normalization of the methylation
dataset have been performed by R packages such as minfi
or RnBeads. Further, we assume that probes and samples
with excessive missingness have been removed (this task can be completed
by subsetting the original methylation data set with the probes and
samples identified by the MarkMissing() function).
# Purge any probes or samples with excessive missing values
markCells_ls <- MarkMissing(dnaM_df = betasChr22_df)
betasChr22_df <- betasChr22_df[
markCells_ls$keepProbes,
markCells_ls$keepSamples
]
# Inspect
betasChr22_df[1:5, 1:5]## GSM1443279 GSM1443663 GSM1443434 GSM1443547 GSM1443577
## cg00004192 0.9249942 0.8463296 0.8700718 0.9058205 0.9090382
## cg00004775 0.6523025 0.6247554 0.7573476 0.6590817 0.6726261
## cg00012194 0.8676339 0.8679048 0.8484754 0.8754985 0.8484458
## cg00013618 0.9466056 0.9475467 0.9566493 0.9588431 0.9419563
## cg00014104 0.3932388 0.5525716 0.4075900 0.3997278 0.3216956The corresponding phenotype dataset included variables
stage (Braak AD stage), subject.id,
slide (batch effect), sex, Sample
and age.brain (age of the brain donor).
## stage subject.id sex Sample age.brain slide
## 3 0 1 Sex: FEMALE GSM1443251 82 6042316048
## 8 2 2 Sex: FEMALE GSM1443256 82 6042316066
## 10 NA 3 Sex: MALE GSM1443258 89 6042316066
## 15 1 4 Sex: FEMALE GSM1443263 81 7786923107
## 21 2 5 Sex: FEMALE GSM1443269 92 6042316121
## 22 1 6 Sex: MALE GSM1443270 78 6042316099Note that only samples with both methylation data and non-missing
phenotype data are analyzed by coMethDMR. So in this
example, the sample with subject.id = 3 which lacks AD
stage information will be excluded from analysis. Please also note the
phenotype file needs to have a variable called “Sample” that will be
used by coMethDMR to link to the methylation
dataset.
As mentioned previously in “Introduction to coMethDMR”, there are several steps in the coMethDMR pipeline:
Suppose we are interested in analyzing genic regions on the 450k
arrays. In the following, closeByGeneAll_ls is a list,
where each item includes at least 3 CpGs located closely (max distance
between 2 CpGs is 200bp by default).
closeByGeneAll_ls <- readRDS(
system.file(
"extdata",
"450k_Gene_3_200.rds",
package = 'coMethDMR',
mustWork = TRUE
)
)We can inspect the first region in the list via:
## $`chr4:91760141-91760229`
## [1] "cg01583657" "cg25325192" "cg06044899"Next, for demonstration, we select regions on chromosome 22.
indx <- grep("chr22:", names(closeByGeneAll_ls))
closeByGene_ls <- closeByGeneAll_ls[indx]
rm(closeByGeneAll_ls)
length(closeByGene_ls)## [1] 676There are 676 genic regions to be tested for chromosome 22. As an example, this vignette will analyze the first 10 regions, which contain the following CpGs:
## $`chr22:30662799-30663041`
## [1] "cg19018155" "cg10467217" "cg24727122" "cg02597698" "cg25666403"
## [6] "cg02026204" "cg05539509" "cg07498879"
##
## $`chr22:18632404-18633123`
## [1] "cg27281093" "cg18699242" "cg01963623" "cg02169692" "cg00077299"
## [6] "cg07964128" "cg02518889" "cg01246421" "cg08205655" "cg10685559"
##
## $`chr22:43253145-43253208`
## [1] "cg15656623" "cg10648908" "cg02351223"
##
## $`chr22:43253517-43253559`
## [1] "cg09861871" "cg00079563" "cg26529516" "cg04527868" "cg01029450"
##
## $`chr22:43254043-43254168`
## [1] "cg23778094" "cg00539564" "cg09367092"
##
## $`chr22:30901532-30901886`
## [1] "cg03214697" "cg00093544" "cg02923264" "cg03014622" "cg19964641"
## [6] "cg15829116" "cg07217063"
##
## $`chr22:39883190-39883347`
## [1] "cg00550928" "cg00101350" "cg26692811"
##
## $`chr22:30685584-30685926`
## [1] "cg00101453" "cg23835894" "cg22088670" "cg03652890" "cg24843389"
## [6] "cg15272908" "cg20395643" "cg10998744"
##
## $`chr22:45064086-45064238`
## [1] "cg10031995" "cg21293611" "cg11450750"
##
## $`chr22:45072455-45072724`
## [1] "cg24019054" "cg20339720" "cg16166559" "cg06849477"In order to make these examples as simple as possible, we will remove the CpGs from our data set which are not included in these 10 regions. In practice, you would keep the full data set.
keepCpGs_char <- unique(unlist(closeByGene_ls[1:10]))
betasChr22small_df <-
betasChr22_df[rownames(betasChr22_df) %in% keepCpGs_char, ]
dim(betasChr22small_df)## [1] 54 20This step removes uninteresting technical and biological effects
using the GetResiduals function, so that the resulting
co-methylated clusters are only driven by the biological factors we are
interested in. Note that there may be an error with the parallel
back-end (1 parallel job did not deliver a result); this
has occurred rarely for us (and not consistently enough for us to create
a reproducible example), but it goes away when we execute the code a
second time. We then recommend that you test this with a smaller subset
of your data first. If you are able to consistently replicate a parallel
error, please submit a bug report: https://github.com/TransBioInfoLab/coMethDMR/issues.
resid_mat <- GetResiduals(
dnam = betasChr22small_df,
# converts to Mvalues for fitting linear model
betaToM = TRUE,
pheno_df = pheno_df,
# Features in pheno_df used as covariates
covariates_char = c("age.brain", "sex", "slide"),
nCores_int = 2
)## Phenotype data is not in the same order as methylation data. We used column Sample in phenotype data to put these two files in the same order.The cluster computing with the BiocParallel package
involves simply changing the default value of one argument:
nCores_int. This argument enables you to perform parallel
computing when you set the number of cores to an integer value greater
than 1. If you do not know how many cores your machine has, use the
detectCores() function from the parallel
package. Note that, if you have many applications open on your computer,
you should not use all of the cores available.
Once we know how many cores we have available, we execute the
CoMethAllRegions() function using each worker in the
cluster, to find co-methylated clusters in the genic regions. As an
example, we only analyze the first 10 CpG regions
(CpGs_ls).
system.time(
coMeth_ls <- CoMethAllRegions(
dnam = resid_mat,
betaToM = FALSE,
method = "spearman",
arrayType = "450k",
CpGs_ls = closeByGene_ls[1:10],
nCores_int = 2
)
)## user system elapsed
## 4.849 0.328 6.050The object coMeth_ls is a list, with each item
containing the list of CpGs within an identified co-methylated
region.
Next we test these co-methylated regions against continuous phenotype
stage, adjusting for covariates age and
sex, by executing the lmmTestAllRegions()
function.
res_df <- lmmTestAllRegions(
betas = betasChr22small_df,
region_ls = coMeth_ls,
pheno_df = pheno_df,
contPheno_char = "stage",
covariates_char = c("age.brain", "sex"),
modelType = "randCoef",
arrayType = "450k",
nCores_int = 2
# outLogFile = "res_lmm_log.txt"
)Model fit messages and diagnostics for each region will be saved to
the log file specified with the outLogFile argument. For a
single region, this will return a one row of model fit statistics
similar to the following:
| chrom | start | end | nCpGs | Estimate | StdErr | Stat | pValue |
|---|---|---|---|---|---|---|---|
| chr22 | 24823455 | 24823519 | 4 | -0.0702 | 0.0290 | -2.4184 | 0.0155 |
Finally, we can annotate these results:
## chrom start end nCpGs Estimate StdErr Stat pValue
## 1 chr22 30662799 30663041 8 -0.059977631 0.01878100 -3.1935273 0.001405461
## 2 chr22 43253521 43253559 4 -0.007602187 0.02873768 -0.2645373 0.791365960
## 3 chr22 30901532 30901886 7 0.018015623 0.01555597 1.1581162 0.246816609
## 4 chr22 39883190 39883347 3 0.069276861 0.02863864 2.4189998 0.015563247
## FDR UCSC_RefGene_Group UCSC_RefGene_Accession
## 1 0.005621842 1stExon;5'UTR;TSS1500;TSS200 NM_020530
## 2 0.791365960 TSS200 NM_001142293;NM_014570
## 3 0.329088811 1stExon;5'UTR;Body;TSS200 NM_001161368;NM_174977
## 4 0.031126493 1stExon;5'UTR;TSS200 NM_001098270;NM_002409
## UCSC_RefGene_Name Relation_to_Island
## 1 OSM OpenSea
## 2 ARFGAP3 Island
## 3 SEC14L4 Island;S_Shore
## 4 MGAT3 N_ShoreIn this section, we provide example scripts for testing genic and intergenic regions using coMethDMR and BiocParallel R packages.
First, we read in clusters of CpGs located closely on the array, in genic and intergenic regions, then combine them into a single list.
closeByGene_ls <- readRDS(
system.file(
"extdata",
"450k_Gene_3_200.rds",
package = 'coMethDMR',
mustWork = TRUE
)
)
closeByInterGene_ls <- readRDS(
system.file(
"extdata",
"450k_InterGene_3_200.rds",
package = 'coMethDMR',
mustWork = TRUE
)
)
# put them together in one list
closeBy_ls <- c(closeByInterGene_ls, closeByGene_ls)
length(closeBy_ls)## [1] 42536## $`chr1:569427-569687`
## [1] "cg08858441" "cg03348902" "cg01070250"
##
## $`chr1:713921-714177`
## [1] "cg10037654" "cg14057946" "cg11422233" "cg16047670" "cg18263059"
## [6] "cg01014490"
##
## $`chr1:834183-834356`
## [1] "cg13938959" "cg12445832" "cg23999112"With this list of regions and their probe IDs, repeat the analysis code in the previous section.
The analysis for EPIC methylation arrays would be the same as those for 450k arrays, except by testing genomic regions in files “EPIC_Gene_3_200.rds” and “EPIC_InterGene_3_200.RDS”, instead of “450k_Gene_3_200.rds” and “450k_InterGene_3_200.rds”. These data sets are available at https://github.com/TransBioInfoLab/coMethDMR_data/tree/main/data.
In this vignette, we have analyzed a small subset of a real EWAS
dataset (i.e. only chromosome 22 data on 20 subjects). To give users a
more realistic estimate of time for analyzing real EWAS datasets, we
also measured time used for analyzing the entire Lunnon et al. (2014)
dataset with 110 samples on all chromosomes. These computation times
measured on a Dell Precision 5810 with 64Gb of RAM, an Intel Xeon
E5-2640 CPU at 2.40Ghz, and using up to 20 cores. More specifically, in
Section 4, the entire coMethDMR workflow for took 103
minutes with 6 cores and used a maximum of 24Gb of RAM (for the
CoMethAllRegions() function). We’re currently working
improving the speed and reducing the size of coMethDMR,
so please check back soon for updates.
## R version 4.4.2 (2024-10-31)
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## attached base packages:
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## [8] base
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## other attached packages:
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## [4] GenomeInfoDb_1.43.2 IRanges_2.41.1 S4Vectors_0.45.2
## [7] BiocGenerics_0.53.3 generics_0.1.3 coMethDMR_1.11.0
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