View source: R/AnnotateResults.R
AnnotateResults | R Documentation |
Add annotations to site-specific or region-based analysis
results from function TestAssociations
.
AnnotateResults( results_df, closeByRegions_gr = NULL, inputRegions_gr = NULL, genome = c("hg38", "hg19"), analysis = c("region-based", "site-specific") )
results_df |
An output data frame from function
|
closeByRegions_gr |
An output GRanges object from function
|
inputRegions_gr |
A GRanges object for input genomic
regions, defaults to |
genome |
Use |
analysis |
Results type. Defaults to |
A data frame with locations of the genomic sites or regions
(seqnames, start, end, width
), annotations for locations
(inputRegion, closeByRegion, symbol
), test statistics
(estimate, stdErr
or coef, exp_coef, se_coef
), pValue
and false discovery rate (fdr
).
TransformToGR
, AllCloseByRegions
,
AllCoeditedRegions
, CreateEditingTable
,
SummarizeAllRegions
, TestAssociations
data(rnaedit_df) # get GRanges for genes genes_gr <- TransformToGR( genes_char = c("PHACTR4", "CCR5", "METTL7A"), type = "symbol", genome = "hg19" ) # find close-by regions within the genes closebyRegions_gr <- AllCloseByRegions( regions_gr = genes_gr, rnaEditMatrix = rnaedit_df ) # identify co-edited regions within the genes coedited_gr <- AllCoeditedRegions( regions_gr = closebyRegions_gr, rnaEditMatrix = rnaedit_df, output = "GRanges", method = "spearman" ) # summarize editing levels within each gene by maximum summarizedRegions_df <- SummarizeAllRegions( regions_gr = coedited_gr, rnaEditMatrix = rnaedit_df, selectMethod = MaxSites ) exm_pheno <- readRDS( system.file( "extdata", "pheno_df.RDS", package = 'rnaEditr', mustWork = TRUE ) ) # test summarized editing levels against survival outcome results_df <- TestAssociations( rnaEdit_df = summarizedRegions_df, pheno_df = exm_pheno, responses_char = "sample_type", covariates_char = NULL, respType = "binary" ) AnnotateResults( results_df = results_df, closeByRegions_gr = closebyRegions_gr, inputRegions_gr = genes_gr, genome = "hg19" )
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