Given a tabular file containing counts of reads overlapping exons or other contigs from two groups (eg treatment, control) of RNA-seq samples with biological replicates, this tool runs edgeR to estimate the probability of each contig being differentially expressed. The companion bams2mx tool is recommended for creating appropriate input files from RNA-seq data mapped to either a transcriptome or genome as BAM files. |
hg clone https://toolshed.g2.bx.psu.edu/repos/fubar/digital_dge
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
for RNA counts | 0.01 | any |