GenomicSuperSignature - Quickstart
October 29, 2024
Abstract
This vigenette demostrates a basic usage of GenomicSuperSignature. More extensive and biology-relavant use cases are available HERE.
Contents
1 Setup
1.1 Install and load package
if (!require("BiocManager"))
install.packages("BiocManager")
BiocManager::install("GenomicSuperSignature")
BiocManager::install("bcellViper")library(GenomicSuperSignature)
library(bcellViper)1.2 Download RAVmodel
You can download GenomicSuperSignature from Google Cloud bucket using
GenomicSuperSignature::getModel function. Currently available models are
built from top 20 PCs of 536 studies (containing 44,890 samples) containing
13,934 common genes from each of 536 study’s top 90% varying genes based on
their study-level standard deviation. There are two versions of this RAVmodel
annotated with different gene sets for GSEA - MSigDB C2 (C2) and three
priors from PLIER package (PLIERpriors).
The demo in this vignette is based on human B-cell expression data, so we are
using the PLIERpriors model annotated with blood-associated gene sets.
Note that the first interactive run of this code, you will be asked to allow
R to create a cache directory. The model file will be stored there and
subsequent calls to getModel will read from the cache.
RAVmodel <- getModel("PLIERpriors", load=TRUE)
#> [1] "downloading"
RAVmodel
#> class: PCAGenomicSignatures
#> dim: 13934 4764
#> metadata(8): cluster size ... version geneSets
#> assays(1): RAVindex
#> rownames(13934): CASKIN1 DDX3Y ... CTC-457E21.9 AC007966.1
#> rowData names(0):
#> colnames(4764): RAV1 RAV2 ... RAV4763 RAV4764
#> colData names(4): RAV studies silhouetteWidth gsea
#> trainingData(2): PCAsummary MeSH
#> trainingData names(536): DRP000987 SRP059172 ... SRP164913 SRP188526
version(RAVmodel)
#> [1] "1.1.1"1.3 Example dataset
The human B-cell dataset (Gene Expression Omnibus series GSE2350) consists of 211 normal and tumor human B-cell phenotypes. This dataset was generated on Affymatrix HG-U95Av2 arrays and stored in an ExpressionSet object with 6,249 features x 211 samples.
data(bcellViper)
dset
#> ExpressionSet (storageMode: lockedEnvironment)
#> assayData: 6249 features, 211 samples
#> element names: exprs
#> protocolData: none
#> phenoData
#> sampleNames: GSM44075 GSM44078 ... GSM44302 (211 total)
#> varLabels: sampleID description detailed_description
#> varMetadata: labelDescription
#> featureData: none
#> experimentData: use 'experimentData(object)'
#> Annotation:You can provide your own expression dataset in any of these formats: simple matrix, ExpressionSet, or SummarizedExperiment. Just make sure that genes are in a ‘symbol’ format.
2 Which RAV best represents the dataset?
validate function calculates validation score, which provides a quantitative
representation of the relevance between a new dataset and RAV. RAVs that give
the validation score is called validated RAV. The validation results can
be displayed in different ways for more intuitive interpretation.
val_all <- validate(dset, RAVmodel)
head(val_all)
#> score PC sw cl_size cl_num
#> RAV1 0.2249382 2 -0.05470163 6 1
#> RAV2 0.3899341 2 0.06426256 21 2
#> RAV3 0.1887409 2 -0.01800335 4 3
#> RAV4 0.2309703 6 -0.04005584 7 4
#> RAV5 0.2017431 2 0.05786189 3 5
#> RAV6 0.1903602 8 -0.02520973 3 62.1 HeatmapTable
heatmapTable takes validation results as its input and displays them into
a two panel table: the top panel shows the average silhouette width (avg.sw)
and the bottom panel displays the validation score.
heatmapTable can display different subsets of the validation output. For
example, if you specify scoreCutoff, any validation result above that score
will be shown. If you specify the number (n) of top validation results through
num.out, the output will be a n-columned heatmap table. You can also use the
average silhouette width (swCutoff), the size of cluster (clsizecutoff),
one of the top 8 PCs from the dataset (whichPC).
Here, we print out top 5 validated RAVs with average silhouette width above 0.
heatmapTable(val_all, RAVmodel, num.out = 5, swCutoff = 0)
2.2 Interactive Graph
Under the default condition, plotValidate plots validation results of all non
single-element RAVs in one graph, where x-axis represents average silhouette
width of the RAVs (a quality control measure of RAVs) and y-axis represents
validation score. We recommend users to focus on RAVs with higher validation
score and use average silhouette width as a secondary criteria.
plotValidate(val_all, interactive = FALSE)
Note that interactive = TRUE will result in a zoomable, interactive plot
that included tooltips.
You can hover each data point for more information:
- sw : the average silhouette width of the cluster
- score : the top validation score between 8 PCs of the dataset and RAVs
- cl_size : the size of RAVs, represented by the dot size
- cl_num : the RAV number. You need this index to find more information
about the RAV.
- PC : test dataset’s PC number that validates the given RAV. Because we used top 8 PCs of the test dataset for validation, there are 8 categories.
If you double-click the PC legend on the right, you will enter an individual display mode where you can add an additional group of data point by single-click.
3 What kinds of information can you access through RAV?
GenomicSuperSignature connects different public databases and prior information through RAVmodel, creating the knowledge graph illustrated below. Through RAVs, you can access and explore the knowledge graph from multiple entry points such as gene expression profiles, publications, study metadata, keywords in MeSH terms and gene sets.
3.1 MeSH terms in wordcloud
You can draw a wordcloud with the enriched MeSH terms of RAVs. Based on the
heatmap table above, three RAVs (2538, 1139, and 884) show the high validation
scores with the positive average silhouette widths, so we draw wordclouds of
those RAVs using drawWordcloud function. You need to provide RAVmodel and
the index of the RAV you are interested in.
Index of validated RAVs can be easily collected using validatedSingatures
function, which outputs the validated index based on num.out, PC from dataset
(whichPC) or any *Cutoff arguments in the same way as heatmapTable. Here,
we choose the top 3 RAVs with the average silhouette width above 0, which will
returns RAV2538, RAV1139, and RAV884 as we discussed above.
validated_ind <- validatedSignatures(val_all, RAVmodel, num.out = 3,
swCutoff = 0, indexOnly = TRUE)
validated_ind
#> [1] 2538 1139 884And we plot the wordcloud of those three RAVs.
set.seed(1) # only if you want to reproduce identical display of the same words
drawWordcloud(RAVmodel, validated_ind[1])
drawWordcloud(RAVmodel, validated_ind[2])
drawWordcloud(RAVmodel, validated_ind[3])
3.2 GSEA
3.2.1 Associated gene sets of validated RAV
You can directly access the GSEA outputs for each RAV using annotateRAV
function. Based on the wordclouds, RAV1139 seems to be associated with B-cell.
annotateRAV(RAVmodel, validated_ind[2]) # RAV1139
#> Description NES pvalue
#> 1 DMAP_ERY3 -2.179082 1e-10
#> 2 KEGG_ALZHEIMERS_DISEASE -2.443701 1e-10
#> 3 REACTOME_POST_TRANSLATIONAL_PROTEIN_MODIFICATION -2.458995 1e-10
#> 4 REACTOME_APOPTOSIS -2.645437 1e-10
#> 5 KEGG_HUNTINGTONS_DISEASE -2.670108 1e-10
#> qvalues
#> 1 6.390977e-10
#> 2 6.390977e-10
#> 3 6.390977e-10
#> 4 6.390977e-10
#> 5 6.390977e-10If you want to check the enriched pathways for multiple RAVs, use
subsetEnrichedPathways function instead.
subsetEnrichedPathways(RAVmodel, validated_ind[2], include_nes = TRUE)
#> DataFrame with 10 rows and 2 columns
#> RAV1139.Description RAV1139.NES
#> <character> <numeric>
#> Up_1 DMAP_ERY3 -2.17908
#> Up_2 KEGG_ALZHEIMERS_DISE.. -2.44370
#> Up_3 REACTOME_POST_TRANSL.. -2.45899
#> Up_4 REACTOME_APOPTOSIS -2.64544
#> Up_5 KEGG_HUNTINGTONS_DIS.. -2.67011
#> Up_6 REACTOME_MRNA_PROCES.. -2.67431
#> Up_7 REACTOME_HOST_INTERA.. -2.69593
#> Up_8 PID_E2F_PATHWAY -2.74887
#> Up_9 KEGG_PYRIMIDINE_META.. -2.75404
#> Up_10 REACTOME_CDK_MEDIATE.. -2.75535
subsetEnrichedPathways(RAVmodel, validated_ind, include_nes = TRUE)
#> DataFrame with 10 rows and 6 columns
#> RAV2538.Description RAV2538.NES RAV1139.Description RAV1139.NES
#> <character> <numeric> <character> <numeric>
#> Up_1 REACTOME_CELL_CYCLE 3.25799 DMAP_ERY3 -2.17908
#> Up_2 REACTOME_CELL_CYCLE_.. 3.22323 KEGG_ALZHEIMERS_DISE.. -2.44370
#> Up_3 REACTOME_DNA_REPLICA.. 3.18974 REACTOME_POST_TRANSL.. -2.45899
#> Up_4 REACTOME_MITOTIC_M_M.. 3.10711 REACTOME_APOPTOSIS -2.64544
#> Up_5 REACTOME_MITOTIC_PRO.. 2.91384 KEGG_HUNTINGTONS_DIS.. -2.67011
#> Up_6 KEGG_CELL_CYCLE 2.86725 REACTOME_MRNA_PROCES.. -2.67431
#> Up_7 REACTOME_CHROMOSOME_.. 2.85931 REACTOME_HOST_INTERA.. -2.69593
#> Up_8 REACTOME_S_PHASE 2.85345 PID_E2F_PATHWAY -2.74887
#> Up_9 REACTOME_MITOTIC_G1_.. 2.83497 KEGG_PYRIMIDINE_META.. -2.75404
#> Up_10 REACTOME_CELL_CYCLE_.. 2.80616 REACTOME_CDK_MEDIATE.. -2.75535
#> RAV884.Description RAV884.NES
#> <character> <numeric>
#> Up_1 DMAP_ERY3 -1.43162
#> Up_2 REACTOME_METABOLISM_.. -1.54368
#> Up_3 KEGG_ALZHEIMERS_DISE.. -1.62716
#> Up_4 KEGG_HUNTINGTONS_DIS.. -1.65062
#> Up_5 KEGG_CELL_CYCLE -1.65473
#> Up_6 REACTOME_MITOTIC_G1_.. -1.67482
#> Up_7 REACTOME_METABOLISM_.. -1.68713
#> Up_8 REACTOME_CELL_CYCLE -1.69922
#> Up_9 REACTOME_CELL_CYCLE_.. -1.72169
#> Up_10 REACTOME_DNA_REPLICA.. -1.767563.2.2 Search enriched pathways through keyword
You can also find the RAVs annotated with the keyword-containing pathways using
findSignature function. Without the k argument, this function outputs a
data frame with two columns: the number of RAVs (Freq column) with the
different numbers of keyword-containing, enriched pathways
(# of keyword-containing pathways column).
Here, we used the keyword, “Bcell”.
findSignature(RAVmodel, "Bcell")
#> # of keyword-containing pathways Freq
#> 1 0 4678
#> 2 1 46
#> 3 2 15
#> 4 3 16
#> 5 4 6
#> 6 5 3There are two RAVs with five keyword-containing pathways (row 6). We can check which RAVs they are.
findSignature(RAVmodel, "Bcell", k = 5)
#> [1] 695 953 1994Enriched pathways are ordered by NES and you can check the rank of any keyword-
containing pathways using findKeywordInRAV.
findKeywordInRAV(RAVmodel, "Bcell", ind = 695)
#> [1] "1|2|3|4|5|6|8 (out of 9)"You can check all enriched pathways of RAV using subsetEnrichedPathways
function. If both=TRUE, both the top and bottom enriched pathways will
be printed.
## Chosen based on validation/MeSH terms
subsetEnrichedPathways(RAVmodel, ind = validated_ind[2], n = 3, both = TRUE)
#> DataFrame with 6 rows and 1 column
#> RAV1139.Description
#> <character>
#> Up_1 DMAP_ERY3
#> Up_2 KEGG_ALZHEIMERS_DISE..
#> Up_3 REACTOME_POST_TRANSL..
#> Down_1 REACTOME_CELL_CYCLE_..
#> Down_2 REACTOME_DNA_REPLICA..
#> Down_3 REACTOME_CELL_CYCLE
## Chosen based on enriched pathways
subsetEnrichedPathways(RAVmodel, ind = 695, n = 3, both = TRUE)
#> DataFrame with 6 rows and 1 column
#> RAV695.Description
#> <character>
#> Up_1 IRIS_Bcell-Memory_Ig..
#> Up_2 DMAP_BCELLA3
#> Up_3 IRIS_Bcell-naive
#> Down_1 SVM B cells memory
#> Down_2 DMAP_BCELLA1
#> Down_3 IRIS_PlasmaCell-From..
subsetEnrichedPathways(RAVmodel, ind = 953, n = 3, both = TRUE)
#> DataFrame with 6 rows and 1 column
#> RAV953.Description
#> <character>
#> Up_1 IRIS_Bcell-Memory_Ig..
#> Up_2 IRIS_Bcell-Memory_IgM
#> Up_3 IRIS_Bcell-naive
#> Down_1 IRIS_Monocyte-Day0
#> Down_2 IRIS_DendriticCell-L..
#> Down_3 IRIS_Monocyte-Day1
subsetEnrichedPathways(RAVmodel, ind = 1994, n = 3, both = TRUE)
#> DataFrame with 6 rows and 1 column
#> RAV1994.Description
#> <character>
#> Up_1 SVM T cells CD4 memo..
#> Up_2 DMAP_TCELLA6
#> Up_3 DMAP_TCELLA8
#> Down_1 IRIS_Bcell-naive
#> Down_2 IRIS_Bcell-Memory_IgM
#> Down_3 IRIS_Bcell-Memory_Ig..4 Session Info
sessionInfo()
#> 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: /home/biocbuild/bbs-3.20-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] stats4 stats graphics grDevices utils datasets methods
#> [8] base
#>
#> other attached packages:
#> [1] bcellViper_1.41.0 GenomicSuperSignature_1.14.0
#> [3] SummarizedExperiment_1.36.0 Biobase_2.66.0
#> [5] GenomicRanges_1.58.0 GenomeInfoDb_1.42.0
#> [7] IRanges_2.40.0 S4Vectors_0.44.0
#> [9] BiocGenerics_0.52.0 MatrixGenerics_1.18.0
#> [11] matrixStats_1.4.1 BiocStyle_2.34.0
#>
#> loaded via a namespace (and not attached):
#> [1] DBI_1.2.3 rlang_1.1.4 magrittr_2.0.3
#> [4] clue_0.3-65 GetoptLong_1.0.5 compiler_4.4.1
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#> [64] carData_3.0-5 foreach_1.5.2 generics_0.1.3
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#> [73] ggsignif_0.6.4 Cairo_1.6-2 grid_4.4.1
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