runEdgeR | R Documentation |
Run edgeR on PhIP-Seq data
runEdgeR( object, threshold.cpm = 0, threshold.prevalence = 0, assay.names = c(logfc = "logfc", prob = "prob"), beadsRR = FALSE, de.method = "exactTest", BPPARAM = BiocParallel::bpparam() )
object |
|
threshold.cpm |
CPM threshold to be considered present in a sample |
threshold.prevalence |
proportion of beads-only samples that surpass
|
assay.names |
named vector specifying the assay names for the log2(fold-change) and exact test p-values. If the vector is not names, the first and second entries are used as defaults |
beadsRR |
logical value specifying whether each beads-only sample should be compared to all other beads-only samples. |
de.method |
character describing which edgeR test for differential expression should be used. Must be one of 'exactTest' or 'glmQLFTest' |
BPPARAM |
|
PhIPData object with log2 estimated fold-changes and p-values for enrichment stored in the assays specified by 'assay.names'.
[BiocParallel::BiocParallelParam]
, beadsRR
sim_data <- readRDS(system.file("extdata", "sim_data.rds", package = "beer")) ## Default back-end evaluation runEdgeR(sim_data) ## Serial runEdgeR(sim_data, BPPARAM = BiocParallel::SerialParam()) ## Snow runEdgeR(sim_data, BPPARAM = BiocParallel::SnowParam()) ## With glmQLFTest runEdgeR(sim_data, de.method = "glmQLFTest")
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