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Rmd | 9cf163e | davetang | 2021-01-28 | GO primer and included visualisations |
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Rmd | 687a6ca | davetang | 2021-01-27 | Gene Ontology Enrichment Analysis |
The Gene Ontology Enrichment Analysis (GOEA) is a typical analysis carried out on transcriptome data. Online tools for performing a GOEA include DAVID, Enrichr, and PANTHER just to name a few. While web-based tools are easy to use, it becomes tedious when you have to analyse (or re-analyse) lots of datasets. Therefore, it is preferable to use a programmatic approach and in this post we will check out some Bioconductor packages that allow to perform a GOEA.
First install the following packages, if necessary, and then load them.
if (!requireNamespace("BiocManager", quietly = TRUE))
install.packages("BiocManager")
my_packages <- c("clusterProfiler",
"GOstats",
"GO.db",
"org.Hs.eg.db")
to_install <- my_packages[!my_packages %in% installed.packages()]
# install missing packages, if any
if (length(to_install) > 0){
BiocManager::install(pkgs = to_install)
}
# load all packages and suppress output of sapply
invisible(sapply(my_packages, library, character.only = TRUE))
Create a positive control where the gene set are composed of genes that are all associated with GO:0007411
(axon guidance); we will use the org.Hs.eg.db
package to achieve this based on the vignette.
Methods that can be applied to AnnotationDbi
objects such as org.Hs.eg.db
include: columns
, keytypes
, keys
, and select
.
Use columns
to find out what data can be retrived using select
.
columns(org.Hs.eg.db)
[1] "ACCNUM" "ALIAS" "ENSEMBL" "ENSEMBLPROT" "ENSEMBLTRANS"
[6] "ENTREZID" "ENZYME" "EVIDENCE" "EVIDENCEALL" "GENENAME"
[11] "GO" "GOALL" "IPI" "MAP" "OMIM"
[16] "ONTOLOGY" "ONTOLOGYALL" "PATH" "PFAM" "PMID"
[21] "PROSITE" "REFSEQ" "SYMBOL" "UCSCKG" "UNIGENE"
[26] "UNIPROT"
Use keytypes
to find out what fields we can use as keys to query the database.
keytypes(org.Hs.eg.db)
[1] "ACCNUM" "ALIAS" "ENSEMBL" "ENSEMBLPROT" "ENSEMBLTRANS"
[6] "ENTREZID" "ENZYME" "EVIDENCE" "EVIDENCEALL" "GENENAME"
[11] "GO" "GOALL" "IPI" "MAP" "OMIM"
[16] "ONTOLOGY" "ONTOLOGYALL" "PATH" "PFAM" "PMID"
[21] "PROSITE" "REFSEQ" "SYMBOL" "UCSCKG" "UNIGENE"
[26] "UNIPROT"
Select all genes with GO:0007411
.
go_to_entrez <- select(org.Hs.eg.db,
keys = "GO:0007411",
columns = "ENTREZID",
keytype = "GO")
'select()' returned 1:many mapping between keys and columns
axon_gene <- unique(go_to_entrez$ENTREZID)
length(axon_gene)
[1] 205
Note that we can also use select
on GO.db
to fetch more information on GO:0007411
.
select(GO.db,
keys = "GO:0007411",
columns = columns(GO.db),
keytype = "GOID")
'select()' returned 1:1 mapping between keys and columns
GOID
1 GO:0007411
DEFINITION
1 The chemotaxis process that directs the migration of an axon growth cone to a specific target site in response to a combination of attractive and repulsive cues.
ONTOLOGY TERM
1 BP axon guidance
To perform the GOEA we need to create a gene background called the universe
and we will use all genes with a GO term. Normally the universe
should be the list of genes that were actually assayed in your transcriptome analysis.
all_go_terms <- keys(org.Hs.eg.db, keytype = "GO")
all_go <- select(org.Hs.eg.db, keys = all_go_terms, columns = c("ENTREZID", "GO"), keytype = "GO")
'select()' returned 1:many mapping between keys and columns
universe <- unique(all_go$ENTREZID)
length(universe)
[1] 20488
The function hyperGTest
will perform the GOEA based on a set of parameters; in this example, we are testing for the over-representation of biological process (BP) terms and using a p-value cutoff of 0.001 or less.
params <- new('GOHyperGParams',
geneIds = axon_gene,
universeGeneIds = universe,
ontology = 'BP',
pvalueCutoff = 0.001,
conditional = FALSE,
testDirection = 'over',
annotation = "org.Hs.eg.db"
)
my_test <- hyperGTest(params)
my_test
Gene to GO BP test for over-representation
4723 GO BP ids tested (1069 have p < 0.001)
Selected gene set size: 205
Gene universe size: 18670
Annotation package: org.Hs.eg
Use summary
to get a summary of the results. The summary contains the GOID
, Pvalue
, OddsRatio
, ExpCount
, Count
, and Size
.
ExpCount
is the expected countCount
is how many instances of that term were actually observed in your gene listSize
is the number that could have been found in your gene list if every instance had turned uphead(summary(my_test))
GOBPID Pvalue OddsRatio ExpCount Count Size
1 GO:0007409 0.00000e+00 Inf 5.138725 205 468
2 GO:0007411 0.00000e+00 Inf 3.030530 205 276
3 GO:0048667 0.00000e+00 Inf 6.401446 205 583
4 GO:0061564 0.00000e+00 Inf 5.643814 205 514
5 GO:0097485 0.00000e+00 Inf 3.041510 205 277
6 GO:0006935 6.87054e-316 Inf 7.071237 205 644
Term
1 axonogenesis
2 axon guidance
3 cell morphogenesis involved in neuron differentiation
4 axon development
5 neuron projection guidance
6 chemotaxis
GO terms associated to axons are enriched as expected. Note that the Count
and Size
for GO:0007411 is not identical even though we had selected all genes associated with GO:0007411. If we manually select Entrez gene IDs using org.Hs.egGO
, we still get the same list of genes.
my_df <- as.data.frame(org.Hs.egGO)
my_idx <- my_df$go_id == "GO:0007411"
length(unique(my_df[my_idx, "gene_id"])) == length(axon_gene)
[1] TRUE
This is probably because genes containing GO terms that are descendants of GO:0007411 are also included.
Gene ontologies (GO) are structured as a directed acyclic graph with GO terms as nodes and their relationships as edges. The most commonly used relationships in GO are:
Below is an example of the is a
and part of
relationships.
We can use the GOBPCHILDREN
annotation map or Bimap from the GO.db package to retrieve all descendants of GO:0007411.
bp_children <- as.list(GOBPCHILDREN)
bp_children[["GO:0007411"]]
isa part of isa
"GO:0008045" "GO:0016198" "GO:0021966"
isa isa isa
"GO:0021967" "GO:0021968" "GO:0021969"
isa isa isa
"GO:0021970" "GO:0021971" "GO:0021972"
isa isa isa
"GO:0031290" "GO:0033563" "GO:0033564"
isa isa part of
"GO:0036514" "GO:0036515" "GO:0048846"
part of part of isa
"GO:0061642" "GO:0061643" "GO:0071678"
isa isa isa
"GO:0071679" "GO:0072499" "GO:0097374"
isa isa part of
"GO:0097376" "GO:0097492" "GO:1902287"
part of regulates negatively regulates
"GO:1902378" "GO:1902667" "GO:1902668"
positively regulates part of part of
"GO:1902669" "GO:1904938" "GO:2001266"
We can include these GO terms in our select
query.
my_keys <- c("GO:0007411", bp_children[["GO:0007411"]])
go_to_entrez_children <- select(org.Hs.eg.db,
keys = my_keys,
columns = "ENTREZID",
keytype = "GO")
'select()' returned 1:many mapping between keys and columns
length(unique(go_to_entrez_children$ENTREZID))
[1] 261
We are still missing some genes that are associated with GO:0007411, which is probably due to the exclusion of descendants in the descendants of GO:0007411. We need to recursively search all terms that are descendants of GO:0007411.
params <- new('GOHyperGParams',
geneIds = unique(go_to_entrez_children$ENTREZID),
universeGeneIds = universe,
ontology = 'BP',
pvalueCutoff = 0.001,
conditional = FALSE,
testDirection = 'over',
annotation = "org.Hs.eg.db"
)
Warning in makeValidParams(.Object): removing geneIds not in universeGeneIds
my_test2 <- hyperGTest(params)
head(summary(my_test2))
GOBPID Pvalue OddsRatio ExpCount Count Size
1 GO:0000902 0 Inf 14.399572 260 1034
2 GO:0000904 0 Inf 10.361007 260 744
3 GO:0006935 0 Inf 8.968399 260 644
4 GO:0007409 0 Inf 6.517408 260 468
5 GO:0007411 0 Inf 3.843599 260 276
6 GO:0031175 0 Inf 13.619711 260 978
Term
1 cell morphogenesis
2 cell morphogenesis involved in differentiation
3 chemotaxis
4 axonogenesis
5 axon guidance
6 neuron projection development
The enrichGO
function in the clusterProfiler
package can also perform a GOEA with FDR control.
my_test3 <- enrichGO(axon_gene,
org.Hs.eg.db,
keyType = "ENTREZID",
ont = "BP",
pvalueCutoff = 0.001,
pAdjustMethod = "BH",
universe,
qvalueCutoff = 0.1,
minGSSize = 10,
maxGSSize = 500,
readable = FALSE)
head(data.frame(my_test3))
ID Description GeneRatio
GO:0007409 GO:0007409 axonogenesis 205/205
GO:0007411 GO:0007411 axon guidance 205/205
GO:0097485 GO:0097485 neuron projection guidance 205/205
GO:0050770 GO:0050770 regulation of axonogenesis 41/205
GO:0008038 GO:0008038 neuron recognition 27/205
GO:0010975 GO:0010975 regulation of neuron projection development 56/205
BgRatio pvalue p.adjust qvalue
GO:0007409 468/18670 0.000000e+00 0.000000e+00 0.000000e+00
GO:0007411 276/18670 0.000000e+00 0.000000e+00 0.000000e+00
GO:0097485 277/18670 0.000000e+00 0.000000e+00 0.000000e+00
GO:0050770 183/18670 2.592496e-42 2.143346e-39 1.300341e-39
GO:0008038 48/18670 3.898825e-41 2.578683e-38 1.564455e-38
GO:0010975 499/18670 1.042084e-40 5.743620e-38 3.484583e-38
geneID
GO:0007409 323/474/627/655/682/1002/1400/1436/1600/1630/1796/1808/1826/1855/1942/1943/1944/1945/1946/1947/1948/1949/1969/2041/2042/2043/2044/2045/2046/2047/2048/2049/2050/2051/2115/2131/2297/2534/2549/2625/2637/2668/2674/2675/2676/2736/2737/2817/2885/2886/2887/2909/3730/3798/3800/3897/3908/3913/4009/4089/4147/4628/4684/4756/4902/4914/4917/4983/5015/5080/5290/5291/5293/5295/5335/5458/5578/5588/5594/5595/5598/5623/5649/5747/5781/5786/5800/5818/5909/5979/6091/6092/6259/6324/6387/6405/6464/6469/6477/6585/6586/6654/6708/6709/6710/6711/6712/6714/6900/7080/7143/7204/7408/7430/7436/7473/7474/7852/7869/8013/8399/8609/8633/8660/8828/8829/8851/9046/9048/9211/9252/9260/9353/9355/9369/9378/9499/9637/9638/9846/10048/10371/10381/10500/10505/10512/10678/10752/10818/11023/11127/11313/23022/23032/23114/23191/23767/23768/26999/27020/27255/30011/51332/51466/53358/54538/55715/55740/55816/56896/57408/57453/57549/57556/57731/59277/59352/64096/64221/64855/84665/85358/89780/90249/91624/91653/128434/133418/137970/151449/152330/170302/219699/220164/223117/283297/284217/284656/285220/374946/375790/389549/644168/654429/729920
GO:0007411 323/474/627/655/682/1002/1400/1436/1600/1630/1796/1808/1826/1855/1942/1943/1944/1945/1946/1947/1948/1949/1969/2041/2042/2043/2044/2045/2046/2047/2048/2049/2050/2051/2115/2131/2297/2534/2549/2625/2637/2668/2674/2675/2676/2736/2737/2817/2885/2886/2887/2909/3730/3798/3800/3897/3908/3913/4009/4089/4147/4628/4684/4756/4902/4914/4917/4983/5015/5080/5290/5291/5293/5295/5335/5458/5578/5588/5594/5595/5598/5623/5649/5747/5781/5786/5800/5818/5909/5979/6091/6092/6259/6324/6387/6405/6464/6469/6477/6585/6586/6654/6708/6709/6710/6711/6712/6714/6900/7080/7143/7204/7408/7430/7436/7473/7474/7852/7869/8013/8399/8609/8633/8660/8828/8829/8851/9046/9048/9211/9252/9260/9353/9355/9369/9378/9499/9637/9638/9846/10048/10371/10381/10500/10505/10512/10678/10752/10818/11023/11127/11313/23022/23032/23114/23191/23767/23768/26999/27020/27255/30011/51332/51466/53358/54538/55715/55740/55816/56896/57408/57453/57549/57556/57731/59277/59352/64096/64221/64855/84665/85358/89780/90249/91624/91653/128434/133418/137970/151449/152330/170302/219699/220164/223117/283297/284217/284656/285220/374946/375790/389549/644168/654429/729920
GO:0097485 323/474/627/655/682/1002/1400/1436/1600/1630/1796/1808/1826/1855/1942/1943/1944/1945/1946/1947/1948/1949/1969/2041/2042/2043/2044/2045/2046/2047/2048/2049/2050/2051/2115/2131/2297/2534/2549/2625/2637/2668/2674/2675/2676/2736/2737/2817/2885/2886/2887/2909/3730/3798/3800/3897/3908/3913/4009/4089/4147/4628/4684/4756/4902/4914/4917/4983/5015/5080/5290/5291/5293/5295/5335/5458/5578/5588/5594/5595/5598/5623/5649/5747/5781/5786/5800/5818/5909/5979/6091/6092/6259/6324/6387/6405/6464/6469/6477/6585/6586/6654/6708/6709/6710/6711/6712/6714/6900/7080/7143/7204/7408/7430/7436/7473/7474/7852/7869/8013/8399/8609/8633/8660/8828/8829/8851/9046/9048/9211/9252/9260/9353/9355/9369/9378/9499/9637/9638/9846/10048/10371/10381/10500/10505/10512/10678/10752/10818/11023/11127/11313/23022/23032/23114/23191/23767/23768/26999/27020/27255/30011/51332/51466/53358/54538/55715/55740/55816/56896/57408/57453/57549/57556/57731/59277/59352/64096/64221/64855/84665/85358/89780/90249/91624/91653/128434/133418/137970/151449/152330/170302/219699/220164/223117/283297/284217/284656/285220/374946/375790/389549/644168/654429/729920
GO:0050770 627/1002/1600/1630/1808/1826/1942/1946/1949/2043/2045/2048/2049/2909/3897/5458/5747/5800/5979/6091/6092/6259/6387/6405/6900/7143/7473/7474/7869/8829/8851/9353/10371/10500/10505/10512/23191/57556/89780/223117/374946
GO:0008038 682/1826/1949/2042/2043/2048/2049/2909/6091/6092/6900/7852/8829/8851/10371/23022/27020/27255/54538/57453/57549/64221/84665/91624/128434/133418/152330
GO:0010975 627/655/1002/1400/1600/1630/1808/1826/1855/1942/1946/1948/1949/2042/2043/2045/2048/2049/2534/2625/2909/3897/4914/5458/5649/5747/5800/5979/6091/6092/6259/6324/6387/6405/6900/7143/7436/7473/7474/7852/7869/8829/8851/9353/9638/10371/10500/10505/10512/23191/27020/57556/85358/89780/223117/374946
Count
GO:0007409 205
GO:0007411 205
GO:0097485 205
GO:0050770 41
GO:0008038 27
GO:0010975 56
The output now includes adjusted p-values and the geneIDs that are associated with a given GO ID. Note that the full list of genes for GO:0007411 is 276 again.
In addition to performing the GOEA, clusterProfiler
also has some nice plotting functions.
Bar plot showing each enriched GO term coloured by the adjusted p-value.
barplot(my_test3, showCategory=10)
Dot plot showing each enriched GO term with associated statistics.
dotplot(my_test3, showCategory=10)
Heat plot showing the enriched GO terms on the y-axis and the genes on the x-axis. Genes with the associated GO term are highlighted.
heatplot(my_test3, showCategory=10)
Enrichment map organises enriched terms into a network with edges connecting overlapping gene sets.
emapplot(my_test3, showCategory = 10)
goplot
shows the gene ontology graph with the enriched GO terms highlighted.
goplot(my_test3)
Warning: ggrepel: 1 unlabeled data points (too many overlaps). Consider
increasing max.overlaps
We can use the biomaRt
package for converting between different gene identifiers and in this example, we will convert Ensembl gene IDs to Entrez gene IDs.
if (!"biomaRt" %in% installed.packages()){
BiocManager::install("biomaRt")
}
library("biomaRt")
We will fetch every Ensembl gene ID and randomly select 10 IDs to convert into Entrez gene IDs.
ensembl <- useMart("ensembl", dataset="hsapiens_gene_ensembl")
Ensembl site unresponsive, trying uswest mirror
Ensembl site unresponsive, trying useast mirror
my_chr <- c(1:22, 'M', 'X', 'Y')
my_ensembl_gene <- getBM(attributes = 'ensembl_gene_id',
filters = 'chromosome_name',
values = my_chr,
mart = ensembl)
head(my_ensembl_gene)
ensembl_gene_id
1 ENSG00000223972
2 ENSG00000227232
3 ENSG00000278267
4 ENSG00000243485
5 ENSG00000284332
6 ENSG00000237613
Select 10 Ensembl gene IDs.
set.seed(1984)
to_convert <- sample(x = my_ensembl_gene$ensembl_gene_id, size = 10, replace = FALSE)
Now to convert the IDs.
to_entrez <- getBM(attributes = c('ensembl_gene_id', 'entrezgene_id'),
filters = 'ensembl_gene_id',
values = to_convert,
mart = ensembl)
to_entrez
ensembl_gene_id entrezgene_id
1 ENSG00000124568 6568
2 ENSG00000131400 9476
3 ENSG00000212191 NA
4 ENSG00000225315 NA
5 ENSG00000228658 NA
6 ENSG00000256659 101927694
7 ENSG00000257890 NA
8 ENSG00000267552 NA
9 ENSG00000280344 NA
10 ENSG00000281133 NA
Note that not all Ensembl IDs have Entrez IDs. We can find out how many Ensembl IDs do not have Entrez IDs.
my_entrez_gene <- getBM(attributes = c('ensembl_gene_id', 'entrezgene_id'),
filters = 'ensembl_gene_id',
values = my_ensembl_gene,
mart = ensembl)
table(is.na(my_entrez_gene$entrezgene_id))
FALSE TRUE
25628 35099
35099 out of 60727 Ensembl gene IDs do not have corresponding Entrez gene IDs. To learn more about the missing Entrez ID values from the Ensembl conversion see this useful post on BioStars.
sessionInfo()
R version 4.0.3 (2020-10-10)
Platform: x86_64-apple-darwin17.0 (64-bit)
Running under: macOS Big Sur 10.16
Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRblas.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRlapack.dylib
locale:
[1] en_AU.UTF-8/en_AU.UTF-8/en_AU.UTF-8/C/en_AU.UTF-8/en_AU.UTF-8
attached base packages:
[1] stats4 parallel stats graphics grDevices utils datasets
[8] methods base
other attached packages:
[1] biomaRt_2.44.4 org.Hs.eg.db_3.11.4 GO.db_3.11.4
[4] GOstats_2.54.0 graph_1.66.0 Category_2.54.0
[7] Matrix_1.3-2 AnnotationDbi_1.50.3 IRanges_2.22.2
[10] S4Vectors_0.26.1 Biobase_2.48.0 BiocGenerics_0.34.0
[13] clusterProfiler_3.16.1 workflowr_1.6.2
loaded via a namespace (and not attached):
[1] fgsea_1.14.0 colorspace_2.0-0 ellipsis_0.3.1
[4] ggridges_0.5.3 rprojroot_2.0.2 qvalue_2.20.0
[7] fs_1.5.0 rstudioapi_0.13 farver_2.0.3
[10] urltools_1.7.3 graphlayouts_0.7.1 ggrepel_0.9.1
[13] bit64_4.0.5 scatterpie_0.1.5 xml2_1.3.2
[16] splines_4.0.3 cachem_1.0.1 GOSemSim_2.14.2
[19] knitr_1.31 polyclip_1.10-0 jsonlite_1.7.2
[22] annotate_1.66.0 dbplyr_2.0.0 ggforce_0.3.2
[25] BiocManager_1.30.10 compiler_4.0.3 httr_1.4.2
[28] rvcheck_0.1.8 assertthat_0.2.1 fastmap_1.1.0
[31] later_1.1.0.1 tweenr_1.0.1 htmltools_0.5.1.1
[34] prettyunits_1.1.1 tools_4.0.3 igraph_1.2.6
[37] gtable_0.3.0 glue_1.4.2 reshape2_1.4.4
[40] DO.db_2.9 dplyr_1.0.3 rappdirs_0.3.2
[43] fastmatch_1.1-0 Rcpp_1.0.6 enrichplot_1.8.1
[46] vctrs_0.3.6 ggraph_2.0.4 xfun_0.20
[49] stringr_1.4.0 lifecycle_0.2.0 XML_3.99-0.5
[52] DOSE_3.14.0 europepmc_0.4 MASS_7.3-53
[55] scales_1.1.1 tidygraph_1.2.0 hms_1.0.0
[58] promises_1.1.1 RBGL_1.64.0 RColorBrewer_1.1-2
[61] curl_4.3 yaml_2.2.1 memoise_2.0.0
[64] gridExtra_2.3 ggplot2_3.3.3 downloader_0.4
[67] triebeard_0.3.0 stringi_1.5.3 RSQLite_2.2.3
[70] highr_0.8 genefilter_1.70.0 BiocParallel_1.22.0
[73] rlang_0.4.10 pkgconfig_2.0.3 bitops_1.0-6
[76] evaluate_0.14 lattice_0.20-41 purrr_0.3.4
[79] labeling_0.4.2 cowplot_1.1.1 bit_4.0.4
[82] tidyselect_1.1.0 AnnotationForge_1.30.1 GSEABase_1.50.1
[85] plyr_1.8.6 magrittr_2.0.1 R6_2.5.0
[88] generics_0.1.0 DBI_1.1.1 withr_2.4.1
[91] pillar_1.4.7 whisker_0.4 survival_3.2-7
[94] RCurl_1.98-1.2 tibble_3.0.5 crayon_1.3.4
[97] BiocFileCache_1.12.1 rmarkdown_2.6 viridis_0.5.1
[100] progress_1.2.2 grid_4.0.3 data.table_1.13.6
[103] Rgraphviz_2.32.0 blob_1.2.1 git2r_0.28.0
[106] digest_0.6.27 xtable_1.8-4 tidyr_1.1.2
[109] httpuv_1.5.5 gridGraphics_0.5-1 openssl_1.4.3
[112] munsell_0.5.0 viridisLite_0.3.0 ggplotify_0.0.5
[115] askpass_1.1