knitr::opts_chunk$set( collapse = TRUE, echo = TRUE, message = FALSE, error = FALSE, comment = "#>", fig.path = "man/figures/" ) pkgdownsite <- !is.null(getOption("PKGDOWN_BUILD"))
The FacileAnalysis package defines a set of analysis tasks over genomic data
in a modular fashion, which requires these data to be stored in a container that
implements the FacileData API (aka a FacileDataStore
).
The over-arching goal of developing analyses within this framework is to enable quick and effortless interrogation of genomic data by enabling a hybrid interactive and code-driven approach to data analysis. Analyses can be either completely code-driven, GUI driven, or some mix of the two.
To achieve this goal, analysis modules break down a general analysis task into smaller constituent steps, the results of which can:
|>
) to perform a complete analysis;shine()
,
viz()
, and report()
methods; andranks()
, signature()
, or compare()
methods.Please refer to the RNA-seq Analysis: The Facile Way to get an idea of how to use these tools when analyzing RNA-seq data.
The analyses implemented within this package are listed below, with links to vignettes that describe their functionality in more detail:
fpca
: Interactive Principal Components Analysesfdge
: Interactive Differential Gene Expression Analysisfsea
: Interactive (Gene) Set Enrichment AnalysisA note on the experimental lifecycle: This package is tagged as "experimental" due to its limited use by a broader audience, and not as a sign of the commitment to its development or how long it has been in (internal) use. As we find the edge cases and pain points in the APIs through broader adoption, we expect to soon move to "maturing" (and eventually "stable") lifecycle.
We'll include an exemplar differential expression analysis here in order to touch on some of the guiding principles of an analysis modules mentioned above.
We have first defined a complete differential expression analysis (fdge
),
by breaking it down into the following steps:
FacileDataStore
to perform the
analysis over;"voom"
, "edgeR-qlf"
,
"limma-trend"
, "limma"
)
iii) advanced options, like the threshold to test against (limma/treat), or
whether to incorporate sample level weightsThe example below identifies genes differentially expression between tumor and normal samples (and controlling for sex) in the "BLCA" indication of the example TCGA dataset included in the FacileData package.
library(FacileData) library(FacileAnalysis) efds <- exampleFacileDataSet() # Step 1: define the samples implicated in our test samples <- filter_samples(efds, indication == "BLCA") # Step 2: define the model (design) for the test model <- flm_def(samples, covariate = "sample_type", numer = "tumor", denom = "normal", batch = "sex") # Step 3: configure the options to run the test, which include the assay that # holds the data used to test and the statistical method/framework we # should use to perform the test vdge <- fdge(model, assay_name = "rnaseq", method = "voom")
Perhaps you prefer the edgeR/QLF analysis framework, instead? No problem, we only need to tweak one of the parameters in the last step of the pipeline:
qdge <- fdge(model, assay_name = "rnaseq", method = "edgeR-qlf")
... or DESeq2, perhaps? No problem, we accept pull requests!
There are a number of S3 methods a FacileAnalysisResult
needs to define in
order to be complete. The shine()
, viz()
, and report()
methods allow
the end-user to interrogate (and report) the results of an analysis at
different levels of interactivity.
Let's take a look at how these work over a FacileDgeAnalysisResult
The shine(aresult, ...)
method provides the richest interactive view over a
FacileAnalysisResult
by launching a shiny gadget that enables
the end-user to fully interrogate the results.
shine(vdge)
The viz(aresult, ...)
methods leverage htmlwidgets to create a
JavaScript-powered interactive view of the analysis result, which is detached
from a running R-process.
viz(vdge)
While the output of the viz()
functions can be used directly in Rmarkdown
reports, report(aresult, ...)
is meant to create a "more complete"
(perhaps multi-htmlwidget) view over the result that can be more suitable
for inclusion into an Rmarkdown report.
cap <- paste( "Differential expression of tumor vs normal samples, in the TCGA bladder", "cancer indication (BLCA)") report(vdge, caption = cap)
The same differential expression analysis that created the vdge
object above
can be performed entirely interactively, with the same results.
We can either start the analysis from the same predefined set of samples, but define the linear model and testing framework to use interactively, by launching a the facile differential gene expression gadget:
vdge2 <- fdgeGadget(samples)
Or we can perform the whole thing via a GUI which lets us select the subset of samples and run the differential expression analysis without using any code at all:
vdge3 <- fdgeGadget(efds)
Assuming the same filtering and testing strategies were selected in the GUI
using the fdgeGadget
calls above, the objects they return will all be
equivalent to the vdge
result, which was entirely generated programmatically.
Note: the screen capture of the fdgeGadget()
above actually corresponds
to the analyses in the RNA-seq the facile way vignette.
Because the packages in the facileverse have not officially been released yet and they also depend heavily on bioconductor packages, we recommend using the BiocManager package for installation.
# install.packages("BiocManager") BiocManager::install("facilebio/FacileAnalysis")
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