methylGSA: Gene Set Analysis for DNA Methylation Datasets
Installation
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.
Introduction
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]).
Supported gene sets and gene ID types
- Gene Ontology (via org.Hs.eg.db [5])
- KEGG (via org.Hs.eg.db [5])
- Reactome (via reactome.db [6])
- User-supplied gene sets. Supported gene input ID types:
- “SYMBOL”
- “ENSEMBL”
- “ENTREZID”
- “REFSEQ”
Supported array types
- Infinium Human Methylation 450K BeadChip (via IlluminaHumanMethylation450kanno.ilmn12.hg19 [7])
- Infinium Methylation EPIC BeadChip (via IlluminaHumanMethylationEPICanno.ilm10b4.hg19 [8])
- User supplied mapping between CpG ID and gene name
Description of methylglm
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:
logit(πi) = β0 + β1xi + β2ci For each gene i, πi = Pr(gene i is in gene set), xi represents negative logarithmic transform of its minimum p-value in differential methylation analysis, and ci 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.
Example
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 1Result 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 ADRA1DThe following code can be used to get the genes in all the pathways in methylglm output.
Description of methylRRA
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 P1, P2, ...Pn 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: ρ = min{Pr(P(1) < P(1)obs), Pr(P(2) < P(2)obs)..., Pr(P(n) < P(n)obs)}
methylRRA supports two approaches to adjust for number of CpGs, ORA
and GSEAPreranked [3]. In ORA approach, for gene i, conversion from ρ 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 ρ 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.
Example
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 |
Description of methylgometh
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.
Other options
methylGSA provides many other options for users to customize the analysis.
array.typeis to specify which array type to use. It is either “450K” or “EPIC”. Default is “450K”. This argument will be ignored ifFullAnnotis provided.FullAnnotis preprocessed mapping between CpG ID and gene name provided by prepareAnnot function. Default is NULL. Check example below for details.groupis the type of CpG to be considered in methylRRA or methylglm. By default,groupis “all”, which means all CpGs are considered regardless of their gene group. Ifgroupis “body”, only CpGs on gene body will be considered. Ifgroupis “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:- body: CpGs whose gene group correspond to “Body” or “1stExon”
- promoter1: CpGs whose gene group correspond to “TSS1500” or “TSS200”
- promoter2: CpGs whose gene group correspond to “TSS1500”, “TSS200”,
“1stExon”, or “5’UTR”
GS.listis 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.idtypeis the type of gene ID in user supplied gene sets. IfGS.listis not empty, then the user is expected to provide gene ID type. Supported ID types are “SYMBOL”, “ENSEMBL”, “ENTREZID”, “REFSEQ”. Default is “SYMBOL”.GS.typeis the published gene sets/pathways to be tested ifGS.listis empty. Supported pathways are “GO” (Gene Ontology), “KEGG”, and “Reactome”. Default is “GO”.minsizeis 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.maxsizeis 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.- In methylRRA,
methodis to specify gene set test method. It is either “ORA” or “GSEA” as described in the previous section. Default is “ORA”. - In methylglm,
parallelis eitherTRUEorFALSEindicating whether parallel should be used. Default isFALSE.
Examples
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 TSPY4To 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 1Below is another example testing Reactome pathways using methylglm.
Visualization
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.
xaxisis 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”.numis to specify the number of genes sets to display on the bar plot. Default is 5.colorbyis a string. Either “pvalue” or “padj”. Default is “padj”.titleis a string. The title to display on the bar plot. Default is NULL.
Session info
R version 4.4.1 (2024-06-14)
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] parallel stats4 stats graphics grDevices utils datasets
[8] methods base
other attached packages:
[1] org.Hs.eg.db_3.20.0
[2] AnnotationDbi_1.69.0
[3] IlluminaHumanMethylation450kanno.ilmn12.hg19_0.6.1
[4] minfi_1.51.0
[5] bumphunter_1.49.0
[6] locfit_1.5-9.10
[7] iterators_1.0.14
[8] foreach_1.5.2
[9] Biostrings_2.75.0
[10] XVector_0.45.0
[11] SummarizedExperiment_1.35.5
[12] Biobase_2.67.0
[13] MatrixGenerics_1.17.1
[14] matrixStats_1.4.1
[15] GenomicRanges_1.57.2
[16] GenomeInfoDb_1.41.2
[17] IRanges_2.39.2
[18] S4Vectors_0.43.2
[19] BiocGenerics_0.53.0
[20] methylGSA_1.25.0
[21] rmarkdown_2.28
loaded via a namespace (and not attached):
[1] later_1.3.2
[2] splines_4.4.1
[3] BiocIO_1.17.0
[4] ggplotify_0.1.2
[5] bitops_1.0-9
[6] tibble_3.2.1
[7] R.oo_1.26.0
[8] preprocessCore_1.67.1
[9] XML_3.99-0.17
[10] lifecycle_1.0.4
[11] lattice_0.22-6
[12] MASS_7.3-61
[13] base64_2.0.2
[14] scrime_1.3.5
[15] magrittr_2.0.3
[16] limma_3.61.12
[17] sass_0.4.9
[18] jquerylib_0.1.4
[19] yaml_2.3.10
[20] httpuv_1.6.15
[21] ggtangle_0.0.3
[22] doRNG_1.8.6
[23] askpass_1.2.1
[24] cowplot_1.1.3
[25] DBI_1.2.3
[26] buildtools_1.0.0
[27] RColorBrewer_1.1-3
[28] abind_1.4-8
[29] zlibbioc_1.51.2
[30] quadprog_1.5-8
[31] purrr_1.0.2
[32] R.utils_2.12.3
[33] RCurl_1.98-1.16
[34] yulab.utils_0.1.7
[35] GenomeInfoDbData_1.2.13
[36] enrichplot_1.25.5
[37] ggrepel_0.9.6
[38] tidytree_0.4.6
[39] maketools_1.3.1
[40] rentrez_1.2.3
[41] reactome.db_1.89.0
[42] genefilter_1.87.0
[43] annotate_1.85.0
[44] DelayedMatrixStats_1.29.0
[45] codetools_0.2-20
[46] DelayedArray_0.33.1
[47] DOSE_4.1.0
[48] xml2_1.3.6
[49] tidyselect_1.2.1
[50] aplot_0.2.3
[51] farver_2.1.2
[52] UCSC.utils_1.1.0
[53] beanplot_1.3.1
[54] illuminaio_0.47.0
[55] GenomicAlignments_1.41.0
[56] jsonlite_1.8.9
[57] multtest_2.61.0
[58] survival_3.7-0
[59] RobustRankAggreg_1.2.1
[60] missMethyl_1.39.14
[61] tools_4.4.1
[62] treeio_1.29.2
[63] Rcpp_1.0.13
[64] glue_1.8.0
[65] SparseArray_1.5.45
[66] xfun_0.48
[67] qvalue_2.37.0
[68] dplyr_1.1.4
[69] HDF5Array_1.33.8
[70] withr_3.0.2
[71] fastmap_1.2.0
[72] rhdf5filters_1.17.0
[73] fansi_1.0.6
[74] openssl_2.2.2
[75] digest_0.6.37
[76] mime_0.12
[77] gridGraphics_0.5-1
[78] R6_2.5.1
[79] colorspace_2.1-1
[80] GO.db_3.20.0
[81] RSQLite_2.3.7
[82] R.methodsS3_1.8.2
[83] utf8_1.2.4
[84] tidyr_1.3.1
[85] generics_0.1.3
[86] data.table_1.16.2
[87] rtracklayer_1.65.0
[88] httr_1.4.7
[89] S4Arrays_1.5.11
[90] pkgconfig_2.0.3
[91] gtable_0.3.6
[92] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
[93] blob_1.2.4
[94] siggenes_1.79.0
[95] sys_3.4.3
[96] clusterProfiler_4.15.0
[97] htmltools_0.5.8.1
[98] fgsea_1.31.6
[99] scales_1.3.0
[100] png_0.1-8
[101] ggfun_0.1.7
[102] knitr_1.48
[103] tzdb_0.4.0
[104] reshape2_1.4.4
[105] rjson_0.2.23
[106] nlme_3.1-166
[107] curl_5.2.3
[108] cachem_1.1.0
[109] rhdf5_2.49.0
[110] stringr_1.5.1
[111] restfulr_0.0.15
[112] GEOquery_2.73.5
[113] pillar_1.9.0
[114] grid_4.4.1
[115] reshape_0.8.9
[116] vctrs_0.6.5
[117] promises_1.3.0
[118] xtable_1.8-4
[119] evaluate_1.0.1
[120] readr_2.1.5
[121] GenomicFeatures_1.57.1
[122] cli_3.6.3
[123] compiler_4.4.1
[124] Rsamtools_2.21.2
[125] rlang_1.1.4
[126] crayon_1.5.3
[127] rngtools_1.5.2
[128] labeling_0.4.3
[129] nor1mix_1.3-3
[130] mclust_6.1.1
[131] plyr_1.8.9
[132] fs_1.6.4
[133] stringi_1.8.4
[134] BiocParallel_1.41.0
[135] munsell_0.5.1
[136] lazyeval_0.2.2
[137] GOSemSim_2.31.2
[138] Matrix_1.7-1
[139] patchwork_1.3.0
[140] hms_1.1.3
[141] sparseMatrixStats_1.17.2
[142] bit64_4.5.2
[143] ggplot2_3.5.1
[144] Rhdf5lib_1.27.0
[145] shiny_1.9.1
[146] KEGGREST_1.45.1
[147] statmod_1.5.0
[148] highr_0.11
[149] igraph_2.1.1
[150] memoise_2.0.1
[151] bslib_0.8.0
[152] ggtree_3.13.2
[153] fastmatch_1.1-4
[154] bit_4.5.0
[155] gson_0.1.0
[156] ape_5.8 References
[1] Geeleher, Paul, Lori Hartnett, Laurance J Egan, Aaron Golden, Raja Affendi Raja Ali, and Cathal Seoighe. 2013. Gene-Set Analysis Is Severely Biased When Applied to Genome-Wide Methylation Data. Bioinformatics 29 (15). Oxford University Press: 1851–7.
[2] Kolde, Raivo, Sven Laur, Priit Adler, and Jaak Vilo. 2012. Robust Rank Aggregation for Gene List Integration and Meta-Analysis. Bioinformatics 28 (4). Oxford University Press: 573–80.
[3] Subramanian, Aravind, Pablo Tamayo, Vamsi K Mootha, Sayan Mukherjee, Benjamin L Ebert, Michael A Gillette, Amanda Paulovich, et al. 2005. Gene Set Enrichment Analysis: A Knowledge-Based Approach for Interpreting Genome-Wide Expression Profiles. Proceedings of the National Academy of Sciences 102 (43). National Acad Sciences: 15545–50.
[4] Phipson, Belinda, Jovana Maksimovic, and Alicia Oshlack. 2015. MissMethyl: An R Package for Analyzing Data from Illumina’s Humanmethylation450 Platform. Bioinformatics 32 (2). Oxford University Press: 286–88.
[5] Carlson M (2018). org.Hs.eg.db: Genome wide annotation for Human. R package version 3.6.0.
[6] Ligtenberg W (2018). reactome.db: A set of annotation maps for reactome. R package version 1.64.0.
[7] Hansen, KD. (2016). IlluminaHumanMethylation450kanno.ilmn12.hg19: Annotation for Illumina’s 450k Methylation Arrays. R Package, Version 0.6.0 1.
[8] Hansen, KD. (2017). IlluminaHumanMethylationEPICanno.ilm10b4.hg19: Annotation for Illumina’s Epic Methylation Arrays. R Package, Version 0.6.0 1.
[9] Mi, Gu, Yanming Di, Sarah Emerson, Jason S Cumbie, and Jeff H Chang. 2012. Length Bias Correction in Gene Ontology Enrichment Analysis Using Logistic Regression. PloS One 7 (10). Public Library of Science: e46128.
[10] Benjamini, Yoav, and Yosef Hochberg. 1995. Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing. Journal of the Royal Statistical Society. Series B (Methodological). JSTOR, 289–300.
[11] Young, Matthew D, Matthew J Wakefield, Gordon K Smyth, and Alicia Oshlack. 2012. Goseq: Gene Ontology Testing for Rna-Seq Datasets. R Bioconductor.
[12] Yu G (2018). enrichplot: Visualization of Functional Enrichment Result. R package version 1.0.2, https://github.com/GuangchuangYu/enrichplot.