A meta analysis on effects of Parkinson’s Disease using Gemma.R
29 October 2024
Package
gemma.R 3.3.0
Contents
library(gemma.R)
library(dplyr)
library(poolr)
library(ggplot2)
library(stringr)Gemma.R contains a large number of datasets representing a wide array of conditions. These datasets are manually annotated by our curators to facilitate discovery and categorization making it a useful tool for meta-analysis.
In this example we search Gemma for datasets comparing healthy controls and patients with Parkinson’s Disease. Our curators use ontology terms to annotate datasets when possible. This allows us to use the MONDO Disease Ontology term “MONDO:0005180” to search for datasets and samples annotated with the term to make sure we are accessing datasets relevant for our purposes with minimal effort.
1 Identifying what to search for
Gemma allows searching for datasets using plain text queries. However for a structured analysis, it is usually more helpful to use ontology terms to make sure we are getting the right datasets. To identify potentially useful ontology terms, we can use search_annotations
annots <- search_annotations("parkinson's")
annots %>% head %>% gemma_kable()| category.name | category.URI | value.name | value.URI |
|---|---|---|---|
| NA | NA | parkinson’s disease | http://www.ebi…/EFO_0002508 |
| NA | NA | parkinson’s disease symptom… | http://www.ebi…/EFO_0600011 |
| NA | NA | wolff-parkinson-white syndrome | http://purl.obolibrary…/HP_0001716 |
| NA | NA | parkinsonism with favorable… | http://purl.obolibrary…/HP_0002548 |
| NA | NA | parkinsonism | http://purl.obolibrary…/HP_0001300 |
| NA | NA | atypical juvenile parkinsonism | http://purl.obolibrary…/MONDO_0018321 |
This will return matching ontology terms within every ontology loaded to Gemma. To identify which ones are actually used to annotate our datasets, you can do
annot_counts <- annots$value.URI %>% sapply(\(x){
attributes(get_datasets(uris = x))$totalElements
})
annots$counts = annot_counts
annots %>% filter(counts>0) %>%
arrange(desc(counts)) %>% gemma_kable()| category.name | category.URI | value.name | value.URI | counts |
|---|---|---|---|---|
| NA | NA | parkinson disease | http://purl.obolibrary…/MONDO_0005180 | 205 |
| NA | NA | late-onset parkinson disease | http://purl.obolibrary…/MONDO_0008199 | 2 |
| NA | NA | young-onset parkinson disease | http://purl.obolibrary…/MONDO_0017279 | 1 |
| NA | NA | amyotrophic lateral scleros… | http://purl.obolibrary…/MONDO_0007104 | 1 |
| NA | NA | x-linked dystonia-parkinsonism | http://purl.obolibrary…/MONDO_0010747 | 1 |
| NA | NA | autosomal dominant parkinso… | http://purl.obolibrary…/MONDO_0008200 | 1 |
2 Querying datasets of interest
The get_datasets function can be used to find datasets of interest,
either using ontology terms or plain text. Since Parkinson’s Disease has an unambiguous
ontology term in the Disease Ontology, we will be using it to avoid acquiring
datasets that tangentially mention the disease in their descriptions. Here we also
limit our results to only include human samples since we are not interested in
models from other species and samples that are explicitly from the brain using the
ontology term for brain. Here we will searching within “allCharacteristics” however other filter properties are available. You can use filter_properties to
access all available properties for anything filterable in Gemma.
Some noteable ones for our purposes would be “allCharacteristics”, which searches within every annotation on a dataset and its samples while we could have also used “experimentalDesign.experimentalFactors.factorValues.characteristics” to specifically look within experimental factors. Instead we will be showing how to limit for relevant contrasts in the next steps for this example.
filter_properties()$dataset %>% head %>% gemma_kable| properties | type | description |
|---|---|---|
| accession.accession | string | NA |
| accession.accessionVersion | string | NA |
| accession.externalDatabase…. | string | NA |
| accession.externalDatabase.id | integer | NA |
| accession.externalDatabase…. | string | NA |
| accession.externalDatabase…. | string | NA |
# getting all resulting datasets using limit and offset arguments
results <- get_datasets(filter = "allCharacteristics.valueUri = http://purl.obolibrary.org/obo/MONDO_0005180 and allCharacteristics.valueUri = http://purl.obolibrary.org/obo/UBERON_0000955",
taxa ='human') %>% get_all_pages()
results %>% select(experiment.shortName,experiment.name) %>% head experiment.shortName
<char>
1: GSE7621
2: GSE7307
3: GSE8397
4: GSE20168
5: GSE20333
6: GSE20146
experiment.name
<char>
1: Expression data of substantia nigra from postmortem human brain of Parkinson's disease patients (PD)
2: Human body index - transcriptional profiling
3: Expression profiling of the Parkinsonian Brain
4: Transcriptional analysis of prefrontal area 9 in Parkinson's disease
5: Gene expression profiling of parkinsonian substantia nigra
6: Expression analysis of dissected GPi in Parkinson's disease3 Filtering the datasets for suitability
While we know that all the resulting datasets were annotated for the term for Parkinson’s Disease, we currently do not know how many of them are comparisons of healthy controls and patients with Parkinson’s Disease. We also do not know if the datasets have batch effects that may affect our findings.
For this example, we decided we should not include data sets that have a batch confound (though that is up to the user). Gemma internally handles batch correction if batch
information is available for the dataset. We will be looking at
experiment.batchEffect column. As explained in the get_datasets
documentation, this column will be set to -1 for datasets where batch
confound is detected, 0 for datasets without available batch information
and to 1 if the data is clear of batch confounds.
results <- results %>% filter(experiment.batchEffect == 1)We now want to ensure that the differential expressions we analyze
compare control and Parkinson’s Disease patients. This information is
available via get_dataset_differential_expression_analyses which
returns the experimental groups for differential expression analyses
performed for the dataset. The columns we are primarily interested in
are baseline.factors which typically
records the control group of the differential expression analysis and
experimental.factors which typically
records the test case
experiment_contrasts <- results$experiment.shortName %>%
lapply(function(x){
out = get_dataset_differential_expression_analyses(x)
}) %>% do.call(rbind,.)The factor we are interested in is Parkinson’s Disease in
experimental.factorValue or
“http://purl.obolibrary.org/obo/MONDO_0005180” in experimental.factors’s value.URI.
We also need to make sure that the baseline that the sample is compared against is
a control experiment, samples annotated with “reference subject role” or “http://purl.obolibrary.org/obo/OBI_0000220”
parkin_contrasts <- experiment_contrasts %>%
filter(factor.category == 'disease') %>%
filter(sapply(experimental.factors,function(x){
"http://purl.obolibrary.org/obo/MONDO_0005180" %in% x$value.URI
}) &
sapply(baseline.factors,function(x){
"http://purl.obolibrary.org/obo/OBI_0000220" %in% x$value.URI
}))Note that while this example attempts to show ways you can automate this process, you should take care to perform some manual examination of the data and determine how independent the contrasts you selected actually are. For instance in our selection, there are two contrasts from the same experiment where differential expression is performed on different brain regions.
dup_exp <- parkin_contrasts$experiment.ID %>%
table %>% {.[.>1]} %>% names
dup_exp[1] "23781"parkin_contrasts %>% filter(experiment.ID %in% dup_exp) result.ID contrast.ID experiment.ID factor.category
<int> <char> <int> <char>
1: 509633 200926 23781 disease
2: 509632 200926 23781 disease
factor.category.URI factor.ID baseline.factors
<char> <char> <list>
1: http://www.ebi.ac.uk/efo/EFO_0000408 41659 disease,....
2: http://www.ebi.ac.uk/efo/EFO_0000408 41659 disease,....
experimental.factors isSubset subsetFactor probes.analyzed genes.analyzed
<list> <lgcl> <list> <int> <int>
1: disease,.... TRUE cell typ.... 11708 10298
2: disease,.... TRUE cell typ.... 12040 10588We should at least make sure that these two contrasts don’t share samples between them, one thing to check is the subsetFactor which might explain why these two separate contrasts exist
parkin_contrasts %>% filter(experiment.ID %in% dup_exp) %>% {.$subsetFactor}[[1]]
category category.URI value
<char> <char> <char>
1: cell type http://www.ebi.ac.uk/efo/EFO_0000324 midbrain dopaminergic neuron
value.URI predicate
<char> <char>
1: http://purl.obolibrary.org/obo/CL_2000097 derives from
predicate.URI object
<char> <char>
1: http://purl.obolibrary.org/obo/RO_0001000 substantia nigra pars compacta
object.URI
<char>
1: http://purl.obolibrary.org/obo/UBERON_0001965
summary
<char>
1: midbrain dopaminergic neuron derives from substantia nigra pars compacta
ID factor.ID factor.category factor.category.URI
<int> <int> <char> <char>
1: 200924 41658 organism part http://www.ebi.ac.uk/efo/EFO_0000635
[[2]]
category category.URI value
<char> <char> <char>
1: cell type http://www.ebi.ac.uk/efo/EFO_0000324 midbrain dopaminergic neuron
value.URI predicate
<char> <char>
1: http://purl.obolibrary.org/obo/CL_2000097 derives from
predicate.URI object
<char> <char>
1: http://purl.obolibrary.org/obo/RO_0001000 ventral tegmental area
object.URI
<char>
1: http://purl.obolibrary.org/obo/UBERON_0002691
summary ID
<char> <int>
1: midbrain dopaminergic neuron derives from ventral tegmental area 200925
factor.ID factor.category factor.category.URI
<int> <char> <char>
1: 41658 <NA> <NA>And we can see that these two contrasts are created to split the samples between different brain regions, therefore do not actually share samples between them.
In the next steps we will be downloading expression data in bulk. If you are here to just try the code out, you can speed the process a bit by limiting the number of experiments to deal with
# arbitrarily select a few datasets
# not executed in this example
parkin_contrasts <- parkin_contrasts[1:5,]Now that we have our relevant contrasts, we can download them using
get_differential_expression_values. This function can be used to download
differential expression fold change and p values, either using the
experiment name/ids or more specifically using the result.IDs
differentials <- parkin_contrasts$result.ID %>% lapply(function(x){
# take the first and only element of the output. the function returns a list
# because single experiments may have multiple resultSets. Here we use the
# resultSet argument to directly access the results we need
get_differential_expression_values(resultSets = x)[[1]]
})
# some datasets might not have all the advertised differential expression results
# calculated due to a variety of factors. here we remove the empty differentials
missing_contrasts <- differentials %>% sapply(nrow) %>% {.==0}
differentials <- differentials[!missing_contrasts]
parkin_contrasts <- parkin_contrasts[!missing_contrasts,]4 Getting the p-values for the condition comparison
differentials is now a list of data frames containing the differential
expression information. To run a simple meta-analysis, we need the p values for
the genes from the relevant contrasts.
condition_diffs <- seq_along(differentials) %>% lapply(function(i){
# iterate over the differentials
diff = differentials[[i]]
# get the contrast information about the differential
contrast = parkin_contrasts[i,]
p_vals = diff[[paste0('contrast_',contrast$contrast.ID,"_pvalue")]]
log2fc = diff[[paste0('contrast_',contrast$contrast.ID,"_log2fc")]]
genes = diff$GeneSymbol
data.frame(genes,p_vals,log2fc)
})
# we can use result.IDs and contrast.IDs to uniquely name this.
# we add the experiment.id for readability
names(condition_diffs) = paste0(parkin_contrasts$experiment.ID,'.',
parkin_contrasts$result.ID,'.',
parkin_contrasts$contrast.ID)
condition_diffs[[1]] %>% head genes p_vals log2fc
1 XIST 3.570e-02 -0.3767
2 DDX3Y 1.000e-04 0.6292
3 XIST 2.100e-02 0.2353
4 SELE 1.519e-13 -3.9249
5 XIST 8.200e-03 0.2929
6 XIST 4.010e-01 -0.12585 Combining the acquired p values
Now that we have acquired the values we need for a meta-analysis from Gemma, we can proceed with any methodology we deem suitable for our analysis.
In this example we will use a very simple approach, Fisher’s combined p-value test.
This is implemented in the fisher function from poolr package. Fisher’s method has the advantage that it operates on the p-values,
which are in the processed differential expression results in Gemma. It has some
disadvantages like ignoring the direction of the expression change (Gemma’s p-values are two-tailed) and is very sensitive
to a single ‘outlier’ p-value, but for this demonstration we’ll go with it.
The first step is to identify which genes are available in our results:
all_genes <- condition_diffs %>% lapply(function(x){
x$genes %>% unique
}) %>% unlist %>% table
# we will remove any gene that doesn't appear in all of the results
# while this criteria is too strict, it does help this example to run
# considerably faster
all_genes <- all_genes[all_genes==max(all_genes)]
all_genes <- names(all_genes)
# remove any probesets matching multiple genes. gemma separates these by using "|"
all_genes <- all_genes[!grepl("|",all_genes,fixed = TRUE)]
# remove the "". This comes from probesets not aligned to any genes
all_genes <- all_genes[all_genes != ""]
all_genes %>% head[1] "A2M" "AAAS" "AACS" "AAGAB" "AAK1" "AAMP" Now we can run the test on every gene, followed by a multiple testing correction.
fisher_results <- all_genes %>% lapply(function(x){
p_vals <- condition_diffs %>% sapply(function(y){
# we will resolve multiple probesets by taking the minimum p value for
# this example
out = y[y$genes == x,]$p_vals
if(length(out) == 0 ||all(is.na(out))){
return(NA)
} else{
return(min(out))
}
})
fold_changes <- condition_diffs %>% sapply(function(y){
pv = y[y$genes == x,]$p_vals
if(length(pv) == 0 ||all(is.na(pv))){
return(NA)
} else{
return(y[y$genes == x,]$log2fc[which.min(pv)])
}
})
median_fc = fold_changes %>% na.omit() %>% median
names(median_fc) = 'Median FC'
combined = p_vals %>% na.omit() %>% fisher() %>% {.$p}
names(combined) = 'Combined'
c(p_vals,combined,median_fc)
}) %>% do.call(rbind,.)
fisher_results <- as.data.frame(fisher_results)
rownames(fisher_results) = all_genes
fisher_results[,'Adjusted'] <- p.adjust(fisher_results[,'Combined'],
method = 'fdr')
fisher_results %>%
arrange(Adjusted) %>%
select(Combined,Adjusted,`Median FC`) %>%
headWe end up with quite a few differentially expressed genes in the meta-analysis (Fisher’s method is very sensitive)
sum(fisher_results$Adjusted<0.05) # FDR<0.05[1] 5316nrow(fisher_results) # number of all genes[1] 6235Next we look at markers of dopaminergic cell types and how they rank compared to other genes. Parkinson’s Disease is a neurodegenerative disorder, leading to death of dopaminergic cells. We should expect them to show up in our results.
# markers are taken from https://www.eneuro.org/content/4/6/ENEURO.0212-17.2017
dopa_markers <- c("ADCYAP1", "ATP2B2", "CACNA2D2",
"CADPS2", "CALB2", "CD200", "CDK5R2", "CELF4", "CHGA", "CHGB",
"CHRNA6", "CLSTN2", "CNTNAP2", "CPLX1", "CYB561", "DLK1", "DPP6",
"ELAVL2", "ENO2", "GABRG2", "GRB10", "GRIA3", "KCNAB2", "KLHL1",
"LIN7B", "MAPK8IP2", "NAPB", "NR4A2", "NRIP3", "HMP19", "NTNG1",
"PCBP3", "PCSK1", "PRKCG", "RESP18", "RET", "RGS8", "RNF157",
"SCG2", "SCN1A", "SLC12A5", "SLC4A10", "SLC6A17", "SLC6A3", "SMS",
"SNCG", "SPINT2", "SPOCK1", "SYP", "SYT4", "TACR3", "TENM1",
"TH", "USP29")
fisher_results %>%
arrange(Combined) %>%
rownames %>%
{.%in% dopa_markers} %>%
which %>%
hist(breaks=20, main = 'Rank distribution of dopaminergic markers')
In agreement with our hypothesis, we can see that the dopaminergic markers tend to have high ranks in our results.
6 Acquiring the expression data for a top gene
Now that we have our results, we can take a look at how the expression of one of our top
genes in these experiments. To do this we will use the get_dataset_expression_for_genes function
to get the expression data. Once we get the expression data for our genes of interest, we will use
the get_dataset_samples function to identify which samples belongs to which experimental group.
Note: as of this writing (early 2023), the Gemma.R methods used in this section are not yet released in Bioconductor; install via devtools to try it out.
For starters, lets look at our top pick and the its p values in the individual datasets, on a log scale:
# the top gene from our results
gene <- fisher_results %>% arrange(Adjusted) %>% .[1,] %>% rownames
p_values <- fisher_results %>%
arrange(Adjusted) %>%
.[1,] %>%
select(-Combined,-`Median FC`,-Adjusted) %>%
unlist %>%
na.omit()
#sum(p_values<0.05)
#length(p_values)
# p values of the result in individual studies
p_values %>% log10() %>%
data.frame(`log p value` = .,dataset = 1:length(.),check.names = FALSE) %>%
ggplot(aes(y = `log p value`,x = dataset)) +
geom_point() +
geom_hline(yintercept = log10(0.05),color = 'firebrick') +
geom_text(y = log10(0.05), x = 0, label = 'p < 0.05',vjust =-1,hjust = -0.1) +
theme_bw() + ggtitle(paste("P-values for top gene (", gene, ") in the data sets")) +
theme(axis.text.x = element_blank())
This shows that the gene is nominally significant in some but not all of the data sets.
To examine this further, our next step is to acquire gene expression data from the
relevant datasets using get_dataset_object. We will use both dataset ids and resultSet ids
when using this function since some of the returned analysis are only performed on a subset
of the data. Providing resultSet ids allows us to harmonize the differential expression
results with expression data by returning the relevant subset.
# we need the NCBI id of the gene in question, lets get that from the original
# results
NCBIid <- differentials[[1]] %>% filter(GeneSymbol == gene) %>% .$NCBIid %>% unique
#NCBIid
expression_frame <- get_dataset_object(datasets = parkin_contrasts$experiment.ID,
resultSets = parkin_contrasts$result.ID,
contrasts = parkin_contrasts$contrast.ID,
genes = NCBIid,type = 'tidy',consolidate = 'pickvar')
# get the contrast names for significance markers
signif_contrasts <- which(p_values < 0.05) %>% namesFinally, we’ll make a plot showing the expression of the gene of interest in all the data sets. This helps us see the extent to which there is evidence of consistent differential expression.
expression_frame <- expression_frame %>%
filter(!is.na(expression)) %>%
# add a column to represent the contrast
dplyr::mutate(contrasts = paste0(experiment.ID,'.',
result.ID,'.',
contrast.ID)) %>%
# simplify the labels
dplyr::mutate(disease = ifelse(disease == 'reference subject role','Control','PD'))
# for adding human readable labels on the plot
labeller <- function(x){
x %>% mutate(contrasts = contrasts %>%
strsplit('.',fixed = TRUE) %>%
purrr::map_chr(1) %>%
{expression_frame$experiment.shortName[match(.,expression_frame$experiment.ID)]})
}
# pass it all to ggplot
expression_frame %>%
ggplot(aes(x = disease,y = expression)) +
facet_wrap(~contrasts,scales = 'free',labeller = labeller) +
theme_bw() +
geom_boxplot(width = 0.5) +
geom_point() + ggtitle(paste("Expression of", gene, " per study")) +
geom_text(data = data.frame(contrasts = signif_contrasts,
expression_frame %>%
group_by(contrasts) %>%
summarise(expression = max(expression)) %>%
.[match(signif_contrasts,.$contrasts),]),
x = 1.5, label = '*',size=5,vjust= 1)
7 Session info
sessionInfo()R Under development (unstable) (2024-10-21 r87258)
Platform: x86_64-pc-linux-gnu
Running under: Ubuntu 24.04.1 LTS
Matrix products: default
BLAS: /home/biocbuild/bbs-3.21-bioc/R/lib/libRblas.so
LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0
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] stringr_1.5.1 poolr_1.1-1
[3] purrr_1.0.2 listviewer_4.0.0
[5] viridis_0.6.5 viridisLite_0.4.2
[7] pheatmap_1.0.12 SummarizedExperiment_1.37.0
[9] Biobase_2.67.0 GenomicRanges_1.59.0
[11] GenomeInfoDb_1.43.0 IRanges_2.41.0
[13] S4Vectors_0.45.0 BiocGenerics_0.53.0
[15] MatrixGenerics_1.19.0 matrixStats_1.4.1
[17] ggrepel_0.9.6 ggplot2_3.5.1
[19] dplyr_1.1.4 data.table_1.16.2
[21] gemma.R_3.3.0 BiocStyle_2.35.0
loaded via a namespace (and not attached):
[1] tidyselect_1.2.1 farver_2.1.2 fastmap_1.2.0
[4] mathjaxr_1.6-0 digest_0.6.37 timechange_0.3.0
[7] lifecycle_1.0.4 magrittr_2.0.3 compiler_4.5.0
[10] rlang_1.1.4 sass_0.4.9 tools_4.5.0
[13] utf8_1.2.4 yaml_2.3.10 knitr_1.48
[16] labeling_0.4.3 S4Arrays_1.7.0 htmlwidgets_1.6.4
[19] bit_4.5.0 curl_5.2.3 DelayedArray_0.33.0
[22] xml2_1.3.6 RColorBrewer_1.1-3 abind_1.4-8
[25] withr_3.0.2 grid_4.5.0 fansi_1.0.6
[28] colorspace_2.1-1 scales_1.3.0 tinytex_0.53
[31] cli_3.6.3 rmarkdown_2.28 crayon_1.5.3
[34] generics_0.1.3 rstudioapi_0.17.1 httr_1.4.7
[37] cachem_1.1.0 zlibbioc_1.53.0 assertthat_0.2.1
[40] BiocManager_1.30.25 XVector_0.47.0 vctrs_0.6.5
[43] Matrix_1.7-1 jsonlite_1.8.9 bookdown_0.41
[46] bit64_4.5.2 magick_2.8.5 systemfonts_1.1.0
[49] tidyr_1.3.1 jquerylib_0.1.4 glue_1.8.0
[52] lubridate_1.9.3 stringi_1.8.4 gtable_0.3.6
[55] UCSC.utils_1.3.0 munsell_0.5.1 tibble_3.2.1
[58] pillar_1.9.0 rappdirs_0.3.3 htmltools_0.5.8.1
[61] GenomeInfoDbData_1.2.13 R6_2.5.1 evaluate_1.0.1
[64] kableExtra_1.4.0 lattice_0.22-6 highr_0.11
[67] memoise_2.0.1 bslib_0.8.0 Rcpp_1.0.13
[70] svglite_2.1.3 gridExtra_2.3 SparseArray_1.7.0
[73] xfun_0.48 pkgconfig_2.0.3