createGeneModelFromRegulatoryRegions,Trena-method | R Documentation |
Create a model for a target gene using a Trena object
## S4 method for signature 'Trena'
createGeneModelFromRegulatoryRegions(
obj,
targetGene,
solverNames,
tbl.regulatoryRegions,
mtx
)
obj |
An object of class Trena |
targetGene |
The name of a target gene to use for building a model |
solverNames |
A character vector containing the solver names to be used for building the model |
tbl.regulatoryRegions |
A data frame of regulatory regions, typically generated by using a filter |
mtx |
An assay matrix of expression data |
A data frame containing the gene model
if(interactive()){ # takes too long for the bioconductor build
# Create a Trena object for human and make a gene model for "MEF2C" using a footprint filter
trena <- Trena("hg38")
chromosome <- "chr5"
mef2c.tss <- 88904257
loc.start <- mef2c.tss - 1000
loc.end <- mef2c.tss + 1000
database.filename <- system.file(package="trena", "extdata", "mef2c.neigborhood.hg38.footprints.db")
database.uri <- sprintf("sqlite://%s", database.filename)
sources <- c(database.uri)
load(system.file(package="trena", "extdata/ampAD.154genes.mef2cTFs.278samples.RData"))
motifs.list <- getRegulatoryChromosomalRegions(trena, chromosome, mef2c.tss-1000, mef2c.tss+1000,
sources, "MEF2C", mef2c.tss)
library(MotifDb)
tbl.motifs.tfs <- associateTranscriptionFactors(MotifDb, motifs.list[[1]], source="MotifDb", expand.rows=TRUE)
model.mef2c <- createGeneModelFromRegulatoryRegions(trena, "MEF2C", c("lasso","ridge","randomforest"),
tbl.motifs.tfs, mtx.sub)
} # if interactive
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