DOKK / manpages / debian 10 / cnvkit / cnvkit-genemetrics.1.en
CNVKIT_GENEMETRICS(1) User Commands CNVKIT_GENEMETRICS(1)

cnvkit_genemetrics - Identify targeted genes with copy number gain or loss.

usage: cnvkit genemetrics [-h] [-s SEGMENT] [-t THRESHOLD] [-m MIN_PROBES]

[--drop-low-coverage] [-y]
[-x {m,y,male,Male,f,x,female,Female}] [-o FILENAME] [--mean] [--median] [--mode] [--stdev] [--sem] [--mad] [--mse] [--iqr] [--bivar] [--ci] [--pi] [-a ALPHA] [-b BOOTSTRAP] filename

Processed sample coverage data file (*.cnr), the output of the 'fix' sub-command.

show this help message and exit
Segmentation calls (.cns), the output of the 'segment' command).
Copy number change threshold to report a gene gain/loss. [Default: 0.2]
Minimum number of covered probes to report a gain/loss. [Default: 3]
Drop very-low-coverage bins before segmentation to avoid false-positive deletions in poor-quality tumor samples.
Assume inputs were normalized to a male reference (i.e. female samples will have +1 log-coverage of chrX; otherwise male samples would have -1 chrX).
Specify the sample's chromosomal sex as male or female. (Otherwise guessed from X and Y coverage).
Output table file name.

Mean log2 value (unweighted).
Median.
Mode (i.e. peak density of log2 values).
Standard deviation.
Standard error of the mean.
Median absolute deviation (standardized).
Mean squared error.
Inter-quartile range.
Tukey's biweight midvariance.
Confidence interval (by bootstrap).
Prediction interval.
Level to estimate confidence and prediction intervals; use with --ci and --pi. [Default: 0.05]
Number of bootstrap iterations to estimate confidence interval; use with --ci. [Default: 100]
March 2019 cnvkit_genemetrics 0.9.5