Description

Add both Wilcoxon test and Kolmogorov-Smirnov test p-values to each CNV output of FREEC

Input

Name
Description
Pattern

0 ()

1 ()

2 ()

Output

Name
Description
Pattern

p_value_txt ()

versions ()

Tools

controlfreec/assesssignificance Documentation

Copy number and genotype annotation from whole genome and whole exome sequencing data.

https://github.com/BoevaLab/FREEC/doi: 10.1093/bioinformatics/btq635License: GPL >=2
Authors