Description Usage Arguments Value
View source: R/run_deq_pipeline.R
A package to conveniently run DESeq2, edgeR, and QNB for the detection of differential methylation in MeRIP/m6A-seq data.
1 2 3 |
input.bams |
vector of control input bam files |
ip.bams |
vector of control IP bam files |
peak.files |
vector of peak file names |
gtf |
location of a gtf file for annotations |
paired.end |
boolean indicating whether reads were paired end (defaults to FALSE) |
outfi |
output file name (defaults to deq.results.txt) |
tool |
which tools to run (options: any combination of d, e, and q; defaults to all: 'deq') |
compare.gene |
whether to calculate changes in gene expression for comparison (highly recommended, defaults to TRUE) |
readlen |
average read length for the data (defaults to 100) |
fraglen |
average fragment length for the data (defaults to 100) – (fraglen-readlen) is used to calculate the extension of reads for counting |
nthreads |
number of threads to run on (defaults to 1) |
input.bams |
vector of treatment input bam files |
ip.bams |
vector of treatment IP bam files |
GRanges object with peaks and estimated changes
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.