To install and load methylGSA
if (!requireNamespace("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("methylGSA")
Depending on the DNA methylation array type, other packages may be needed before running the analysis.
If analyzing 450K array, IlluminaHumanMethylation450kanno.ilmn12.hg19
needs to be loaded.
If analyzing EPIC array, IlluminaHumanMethylationEPICanno.ilm10b4.hg19
needs to be loaded.
If analyzing user-supplied mapping between CpG ID and gene name, neither IlluminaHumanMethylation450kanno.ilmn12.hg19
nor IlluminaHumanMethylationEPICanno.ilm10b4.hg19
needs to be loaded.
The methylGSA package contains functions to carry out gene set analysis adjusting for the number of CpGs per gene. It has been shown by Geeleher et al [1] that gene set analysis is extremely biased for DNA methylation data. This package contains three main functions to adjust for the bias in gene set analysis.
methylglm: Incorporating number of CpGs as a covariate in logistic regression.
methylRRA: Adjusting for multiple p-values of each gene by Robust Rank Aggregation [2], and then apply either over-representation analysis (ORA) or Preranked version of Gene Set Enrichment Analysis (GSEAPreranked) [3] in gene set testing.
methylgometh: Adjusting the number of CpGs for each gene by weighted resampling and Wallenius non-central hypergeometric approximation (via missMethyl [4]).
methylglm is an extention of GOglm [9]. GOglm adjusts length bias for RNA-Seq data by incorporating gene length as a covariate in logistic regression model. methylglm adjusts length bias in DNA methylation by the number of CpGs instead of gene length. For each gene set, we fit a logistic regression model:
\[ \text{logit} (\pi_{i}) = \beta_{0} + \beta_{1}x_{i} + \beta_{2}c_{i}\] For each gene \(i\), \(\pi_{i}\) = Pr(gene \(i\) is in gene set), \(x_{i}\) represents negative logarithmic transform of its minimum p-value in differential methylation analysis, and \(c_{i}\) is logarithmic transform of its number of CpGs.
methylglm requires only a simple named vector. This vector contains p-values of each CpG. Names should be their corresponding CpG IDs.
Here is what the input vector looks like:
cg00050873 cg00212031 cg00214611 cg01707559 cg02004872 cg02011394 cg02050847
0.2876 0.7883 0.4090 0.8830 0.9405 0.0456 0.5281
cg02233190 cg02494853 cg02839557 cg02842889 cg03052502 cg03244189 cg03443143
0.8924 0.5514 0.4566 0.9568 0.4533 0.6776 0.5726
cg03683899 cg03706273 cg03750315 cg04016144 cg04042030 cg04448376
0.1029 0.8998 0.2461 0.0421 0.3279 0.9545
Please note that the p-values presented here in cpg.pval
is for illustration purpose only. They are used to show how to utilize the functions in methylGSA. It does not represent p-values from any real data analysis. The actual p-values in differential methylation analysis may be quite different from the p-values in cpg.pval
in terms of the magnitude.
Run methylglm:
res1 = methylglm(cpg.pval = cpg.pval, minsize = 200,
maxsize = 500, GS.type = "KEGG")
head(res1, 15)
ID Description Size pvalue padj
04080 04080 Neuroactive ligand-receptor interaction 272 0.4811308 1
04060 04060 Cytokine-cytokine receptor interaction 265 0.6961531 1
04010 04010 MAPK signaling pathway 268 1.0000000 1
04144 04144 Endocytosis 201 1.0000000 1
04510 04510 Focal adhesion 200 1.0000000 1
04740 04740 Olfactory transduction 388 1.0000000 1
04810 04810 Regulation of actin cytoskeleton 213 1.0000000 1
05200 05200 Pathways in cancer 326 1.0000000 1
Result is a data frame ranked by p-values of gene sets. The meaning of each column is given below.
Column | Explanation |
---|---|
ID | Gene set ID |
Description (N/A for user supplied gene set) | Gene set description |
Size | Number of genes in gene set |
pvalue | p-value in logistic regression |
padj | Adjusted p-value |
Bioconductor package org.Hs.eg.db can be used to pull out the genes corresponding a specific pathway. For instance, one of the pathways in the methylglm output above is “Neuroactive ligand-receptor interaction” with KEGG ID 04080. The following code can be used to obtain its genes.
library(org.Hs.eg.db)
genes_04080 = select(org.Hs.eg.db, "04080", "SYMBOL", keytype = "PATH")
head(genes_04080)
PATH SYMBOL
1 04080 ADCYAP1R1
2 04080 ADORA1
3 04080 ADORA2A
4 04080 ADORA2B
5 04080 ADORA3
6 04080 ADRA1D
The following code can be used to get the genes in all the pathways in methylglm output.
Robust rank aggregation [2] is a parameter free model that aggregates several ranked gene lists into a single gene list. The aggregation assumes random order of input lists and assign each gene a p-value based on order statistics. We apply this order statistics idea to adjust for number of CpGs.
For gene \(i\), let \(P_{1}, P_{2}, ... P_{n}\) be the p-values of individual CpGs in differential methylation analysis. Under the null hypothesis, \(P_{1}, P_{2}, ... P_{n} ~ \overset{i.i.d}{\sim} Unif[0, 1]\). Let \(P_{(1)}, P_{(2)}, ... P_{(n)}\) be the order statistics. Define: \[\rho = \text{min}\{\text{Pr}(P_{(1)}<P_{(1)\text{obs}}), \text{Pr}(P_{(2)}<P_{(2)\text{obs}})..., \text{Pr}(P_{(n)}<P_{(n)\text{obs}}) \} \]
methylRRA supports two approaches to adjust for number of CpGs, ORA and GSEAPreranked [3]. In ORA approach, for gene \(i\), conversion from \(\rho\) score into p-value is done by Bonferroni correction [2]. We get a p-value for each gene and these p-values are then corrected for multiple testing use Benjamini & Hochberg procedure [10]. By default, genes with False Discovery Rate (FDR) below 0.05 are considered differentially expressed (DE) genes. If there are no DE genes under FDR 0.05, users are able to use sig.cut
option to specify a higher FDR cut-off or topDE
option to declare top genes to be differentially expressed. We then apply ORA based on these DE genes.
In GSEAPreranked approach, for gene \(i\), we also convert \(\rho\) score into p-value by Bonferroni correction. p-values are converted into z-scores. We then apply Preranked version of Gene Set Enrichment Analysis (GSEAPreranked) on the gene list ranked by the z-scores.
To apply ORA approach, we use argument method = "ORA"
(default) in methylRRA
The meaning of each column in the output is given below.
Column | Explanation |
---|---|
ID | Gene set ID |
Description (N/A for user supplied gene set) | Gene set description |
Count | Number of significant genes in the gene set |
overlap | Names of significant genes in the gene set |
Size | Number of genes in gene set |
pvalue | p-value in ORA |
padj | Adjusted p-value |
To apply GSEAPreranked approach, we use argument method = "GSEA"
in methylRRA
The meaning of each column in the output is given below.
Column | Explanation |
---|---|
ID | Gene set ID |
Description (N/A for user supplied gene set) | Gene set description |
Size | Number of genes in gene set |
enrichmentScore | Enrichment score (see [3] for details) |
NES | Normalized enrichment score (see [3] for details) |
pvalue | p-value in GSEA |
padj | Adjusted p-value |
methylgometh calls gometh
or gsameth
function in missMethyl package [4] to adjust number of CpGs in gene set testing. gometh
modifies goseq method [11] by fitting a probability weighting function and resampling from Wallenius non-central hypergeometric distribution.
methylgometh requires two inputs, cpg.pval
and sig.cut
. sig.cut
specifies the cut-off point to declare a CpG as differentially methylated. By default, sig.cut
is 0.001. Similar to methylRRA, if no CpG is significant, users are able to specify a higher cut-off or use topDE
option to declare top CpGs to be differentially methylated.
methylGSA provides many other options for users to customize the analysis.
array.type
is to specify which array type to use. It is either “450K” or “EPIC”. Default is “450K”. This argument will be ignored if FullAnnot
is provided.FullAnnot
is preprocessed mapping between CpG ID and gene name provided by prepareAnnot function. Default is NULL. Check example below for details.group
is the type of CpG to be considered in methylRRA or methylglm. By default, group
is “all”, which means all CpGs are considered regardless of their gene group. If group
is “body”, only CpGs on gene body will be considered. If group
is “promoter1” or “promoter2”, only CpGs on promoters will be considered. Based on the annotation in IlluminaHumanMethylation450kanno.ilmn12.hg19 and IlluminaHumanMethylationEPICanno.ilm10b4.hg19, “body”, “promoter1” and “promoter2” are defined as:
GS.list
is user supplied gene sets to be tested. It should be a list with entry names gene set IDs and elements correpond to genes that gene set contain. If there is no input list, Gene Ontology is used by default.GS.idtype
is the type of gene ID in user supplied gene sets. If GS.list
is not empty, then the user is expected to provide gene ID type. Supported ID types are “SYMBOL”, “ENSEMBL”, “ENTREZID”, “REFSEQ”. Default is “SYMBOL”.GS.type
is the published gene sets/pathways to be tested if GS.list
is empty. Supported pathways are “GO” (Gene Ontology), “KEGG”, and “Reactome”. Default is “GO”.minsize
is an integer. If the number of genes in a gene set is less than this integer, this gene set is not tested. Default is 100.maxsize
is also an integer. If the number of genes in a gene set is greater than this integer, this gene set is not tested. Default is 500.method
is to specify gene set test method. It is either “ORA” or “GSEA” as described in the previous section. Default is “ORA”.parallel
is either TRUE
or FALSE
indicating whether parallel should be used. Default is FALSE
.An example of user supplied gene sets is given below. The gene ID type is gene symbol.
data(GSlisttoy)
## to make the display compact, only a proportion of each gene set is shown
head(lapply(GS.list, function(x) x[1:30]), 3)
$GS1
[1] "ABCA11P" "ACOT1" "ACSM2A" "ADAMTS4" "ADH4" "AGTR2"
[7] "AMAC1" "AMY1B" "AMY2A" "ANKRD13C" "ANKRD20A1" "ANKRD20A3"
[13] "ANKRD20A4" "ANXA2P3" "ANXA8" "ANXA8L1" "ARGFXP2" "ARL17B"
[19] "ATF5" "ATP5F1" "BAGE2" "BCL8" "BET3L" "C12orf24"
[25] "C15orf62" "C16orf93" "C17orf86" "C19orf70" "C1orf182" "C22orf29"
$GS2
[1] "KRTAP5-5" "KRTAP6-1" "KRTAP9-8" "KTI12" "LASS1"
[6] "LCMT2" "LGALS9B" "LOC100093631" "LOC100101115" "LOC100101266"
[11] "LOC100130264" "LOC100130932" "LOC100131193" "LOC100131726" "LOC100132247"
[16] "LOC100132832" "LOC100133920" "LOC100286938" "LOC144438" "LOC145820"
[21] "LOC148413" "LOC202781" "LOC286367" "LOC339047" "LOC388499"
[26] "LOC392196" "LOC399753" "LOC440895" "LOC441294" "LOC441455"
$GS3
[1] "SNORA17" "SNORA23" "SNORA25" "SNORA2B" "SNORA31"
[6] "SNORA36C" "SNORA64" "SNORD11" "SNORD113-5" "SNORD113-7"
[11] "SNORD114-1" "SNORD114-16" "SNORD114-17" "SNORD114-18" "SNORD114-21"
[16] "SNORD114-27" "SNORD114-28" "SNORD114-5" "SNORD114-6" "SNORD114-8"
[21] "SNORD114-9" "SNORD116-16" "SNORD116-26" "SNORD116-29" "SNORD12"
[26] "SNORD125" "SNORD126" "SNORD16" "SNORD38B" "SNORD50A"
Below is an example of running methylglm with parallel option
library(BiocParallel)
res_p = methylglm(cpg.pval = cpg.pval, minsize = 200,
maxsize = 500, GS.type = "KEGG", parallel = TRUE)
methylglm and methylRRA support user supplied CpG ID to gene mapping. The mapping is expected to be a matrix, or a data frame or a list. For a matrix or data frame, 1st column should be CpG ID and 2nd column should be gene name. For a list, entry names should be gene names and elements correpond to CpG IDs. Below an example of user supplied CpG to gene mapping.
CpG Gene
1 cg00050873 TSPY4
2 cg00212031 TTTY14
3 cg00214611 TMSB4Y
4 cg01707559 TBL1Y
5 cg02004872 TMSB4Y
6 cg02011394 TSPY4
To use user supplied mapping in methylglm or methylRRA, first preprocess the mapping by prepareAnnot function
Test the gene sets using “ORA” in methylRRA, use FullAnnot
argument to provide the preprocessed CpG ID to gene mapping
GS.list = GS.list[1:10]
res5 = methylRRA(cpg.pval = cpg.pval, FullAnnot = FullAnnot, method = "ORA",
GS.list = GS.list, GS.idtype = "SYMBOL",
minsize = 100, maxsize = 300)
head(res5, 10)
ID Count Size pvalue padj
GS1 GS1 0 157 1 1
GS2 GS2 0 257 1 1
GS3 GS3 0 181 1 1
GS4 GS4 0 274 1 1
GS5 GS5 0 285 1 1
GS6 GS6 0 108 1 1
GS7 GS7 0 202 1 1
GS8 GS8 0 273 1 1
GS9 GS9 0 206 1 1
GS10 GS10 0 187 1 1
Below is another example testing Reactome pathways using methylglm.
Following bar plot implemented in enrichplot [12], we also provide bar plot to visualize the gene set analysis results. The input of barplot
function can be any result returned by methylglm, methylRRA, or methylgometh. Various options are provided for users to customize the plot.
xaxis
is to specify the label in x-axis. It is either “Count” (number of significant genes in gene set) or “Size” (total number of genes in gene set). “Count” option is not available for methylglm and methylRRA(GSEA). Default is “Size”.num
is to specify the number of genes sets to display on the bar plot. Default is 5.colorby
is a string. Either “pvalue” or “padj”. Default is “padj”.title
is a string. The title to display on the bar plot. Default is NULL.R version 4.4.0 RC (2024-04-16 r86468)
Platform: x86_64-pc-linux-gnu
Running under: Ubuntu 22.04.4 LTS
Matrix products: default
BLAS: /home/biocbuild/bbs-3.20-bioc/R/lib/libRblas.so
LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_GB 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: America/New_York
tzcode source: system (glibc)
attached base packages:
[1] parallel stats4 stats graphics grDevices utils datasets
[8] methods base
other attached packages:
[1] org.Hs.eg.db_3.19.1
[2] AnnotationDbi_1.67.0
[3] IlluminaHumanMethylation450kanno.ilmn12.hg19_0.6.1
[4] minfi_1.51.0
[5] bumphunter_1.47.0
[6] locfit_1.5-9.9
[7] iterators_1.0.14
[8] foreach_1.5.2
[9] Biostrings_2.73.0
[10] XVector_0.45.0
[11] SummarizedExperiment_1.35.0
[12] Biobase_2.65.0
[13] MatrixGenerics_1.17.0
[14] matrixStats_1.3.0
[15] GenomicRanges_1.57.0
[16] GenomeInfoDb_1.41.0
[17] IRanges_2.39.0
[18] S4Vectors_0.43.0
[19] BiocGenerics_0.51.0
[20] methylGSA_1.23.0
loaded via a namespace (and not attached):
[1] later_1.3.2
[2] splines_4.4.0
[3] BiocIO_1.15.0
[4] ggplotify_0.1.2
[5] bitops_1.0-7
[6] tibble_3.2.1
[7] polyclip_1.10-6
[8] preprocessCore_1.67.0
[9] XML_3.99-0.16.1
[10] lifecycle_1.0.4
[11] lattice_0.22-6
[12] MASS_7.3-60.2
[13] base64_2.0.1
[14] scrime_1.3.5
[15] magrittr_2.0.3
[16] limma_3.61.0
[17] sass_0.4.9
[18] rmarkdown_2.26
[19] jquerylib_0.1.4
[20] yaml_2.3.8
[21] httpuv_1.6.15
[22] doRNG_1.8.6
[23] askpass_1.2.0
[24] cowplot_1.1.3
[25] DBI_1.2.2
[26] RColorBrewer_1.1-3
[27] abind_1.4-5
[28] zlibbioc_1.51.0
[29] quadprog_1.5-8
[30] purrr_1.0.2
[31] ggraph_2.2.1
[32] RCurl_1.98-1.14
[33] yulab.utils_0.1.4
[34] tweenr_2.0.3
[35] GenomeInfoDbData_1.2.12
[36] enrichplot_1.25.0
[37] ggrepel_0.9.5
[38] tidytree_0.4.6
[39] reactome.db_1.88.0
[40] genefilter_1.87.0
[41] annotate_1.83.0
[42] DelayedMatrixStats_1.27.0
[43] codetools_0.2-20
[44] DelayedArray_0.31.0
[45] DOSE_3.31.0
[46] xml2_1.3.6
[47] ggforce_0.4.2
[48] tidyselect_1.2.1
[49] aplot_0.2.2
[50] UCSC.utils_1.1.0
[51] farver_2.1.1
[52] viridis_0.6.5
[53] beanplot_1.3.1
[54] illuminaio_0.47.0
[55] GenomicAlignments_1.41.0
[56] jsonlite_1.8.8
[57] multtest_2.61.0
[58] tidygraph_1.3.1
[59] survival_3.6-4
[60] RobustRankAggreg_1.2.1
[61] missMethyl_1.39.0
[62] tools_4.4.0
[63] treeio_1.29.0
[64] Rcpp_1.0.12
[65] glue_1.7.0
[66] gridExtra_2.3
[67] SparseArray_1.5.0
[68] xfun_0.43
[69] qvalue_2.37.0
[70] dplyr_1.1.4
[71] HDF5Array_1.33.0
[72] withr_3.0.0
[73] fastmap_1.1.1
[74] rhdf5filters_1.17.0
[75] fansi_1.0.6
[76] openssl_2.1.2
[77] digest_0.6.35
[78] mime_0.12
[79] gridGraphics_0.5-1
[80] R6_2.5.1
[81] colorspace_2.1-0
[82] GO.db_3.19.1
[83] RSQLite_2.3.6
[84] utf8_1.2.4
[85] tidyr_1.3.1
[86] generics_0.1.3
[87] data.table_1.15.4
[88] rtracklayer_1.65.0
[89] graphlayouts_1.1.1
[90] httr_1.4.7
[91] S4Arrays_1.5.0
[92] scatterpie_0.2.2
[93] pkgconfig_2.0.3
[94] gtable_0.3.5
[95] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
[96] blob_1.2.4
[97] siggenes_1.79.0
[98] shadowtext_0.1.3
[99] clusterProfiler_4.13.0
[100] htmltools_0.5.8.1
[101] fgsea_1.31.0
[102] scales_1.3.0
[103] png_0.1-8
[104] ggfun_0.1.4
[105] knitr_1.46
[106] tzdb_0.4.0
[107] reshape2_1.4.4
[108] rjson_0.2.21
[109] nlme_3.1-164
[110] curl_5.2.1
[111] cachem_1.0.8
[112] rhdf5_2.49.0
[113] stringr_1.5.1
[114] HDO.db_0.99.1
[115] restfulr_0.0.15
[116] GEOquery_2.73.0
[117] pillar_1.9.0
[118] grid_4.4.0
[119] reshape_0.8.9
[120] vctrs_0.6.5
[121] promises_1.3.0
[122] xtable_1.8-4
[123] evaluate_0.23
[124] readr_2.1.5
[125] GenomicFeatures_1.57.0
[126] cli_3.6.2
[127] compiler_4.4.0
[128] Rsamtools_2.21.0
[129] rlang_1.1.3
[130] crayon_1.5.2
[131] rngtools_1.5.2
[132] labeling_0.4.3
[133] nor1mix_1.3-3
[134] mclust_6.1.1
[135] plyr_1.8.9
[136] fs_1.6.4
[137] stringi_1.8.3
[138] viridisLite_0.4.2
[139] BiocParallel_1.39.0
[140] munsell_0.5.1
[141] lazyeval_0.2.2
[142] GOSemSim_2.31.0
[143] Matrix_1.7-0
[144] patchwork_1.2.0
[145] hms_1.1.3
[146] sparseMatrixStats_1.17.0
[147] bit64_4.0.5
[148] ggplot2_3.5.1
[149] Rhdf5lib_1.27.0
[150] shiny_1.8.1.1
[151] KEGGREST_1.45.0
[152] statmod_1.5.0
[153] highr_0.10
[154] igraph_2.0.3
[155] memoise_2.0.1
[156] bslib_0.7.0
[157] ggtree_3.13.0
[158] fastmatch_1.1-4
[159] bit_4.0.5
[160] gson_0.1.0
[161] ape_5.8
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