Provided by: rsem_1.3.3+dfsg-2_amd64 

NAME
rsem-control-fdr - Filter EBSeq output for statistical significance.
SYNOPSIS
rsem-control-fdr [options] input_file fdr_rate output_file
ARGUMENTS
input_file
This should be the main result file generated by 'rsem-run-ebseq', which contains all
genes/transcripts and their associated statistics.
fdr_rate
The desire false discovery rate (FDR).
output_file
This file is a subset of the 'input_file'. It only contains the genes/transcripts called as
differentially expressed (DE). When more than 2 conditions exist, DE is defined as not all conditions
are equally expressed. Because statistical significance does not necessarily mean biological
significance, users should also refer to the fold changes to decide which genes/transcripts are
biologically significant. When more than two conditions exist, this file will not contain fold change
information and users need to calculate it from 'input_file.condmeans' by themselves.
OPTIONS
--hard-threshold
Use hard threshold method to control FDR. If this option is set, only those genes/transcripts with
their PPDE >= 1 - fdr_rate are called as DE. (Default: on)
--soft-threshold
Use soft threshold method to control FDR. If this option is set, this program will try to report as
many genes/transcripts as possible, as long as their average PPDE >= 1 - fdr_rate. This option is
equivalent to use EBSeq's 'crit_fun' for FDR control. (Default: off)
-h/--help
Show help information.
DESCRIPTION
This program controls the false discovery rate and reports differentially expressed genes/transcripts.
EXAMPLES
We assume that we have 'GeneMat.results' as input. We want to control FDR at 0.05 using hard threshold
method and name the output file as 'GeneMat.de.txt':
rsem-control-fdr GeneMat.results 0.05 GeneMat.de.txt
perl v5.32.1 2021-09-09 RSEM-CONTROL-FDR(1)