Provided by: cnvkit_0.9.10-2_all
NAME
cnvkit_heatmap - Plot copy number for multiple samples as a heatmap.
DESCRIPTION
usage: cnvkit.py heatmap [-h] [-c CHROMOSOME] [-y] [-x {m,y,male,Male,f,x,female,Female}] [--no-shift-xy] [-o FILENAME] [-b] [-d] [-v] [--delimit-samples] [-t TITLE] filenames [filenames ...] positional arguments: filenames Sample coverages as raw probes (.cnr) or segments (.cns). options: -h, --help show this help message and exit -c CHROMOSOME, --chromosome CHROMOSOME Chromosome (e.g. 'chr1') or chromosomal range (e.g. 'chr1:2333000-2444000') to display. If a range is given, all targeted genes in this range will be shown, unless '--gene'/'-g' is already given. -y, --male-reference, --haploid-x-reference Assume inputs were normalized to a male reference (i.e. female samples will have +1 log-CNR of chrX; otherwise male samples would have -1 chrX). -x {m,y,male,Male,f,x,female,Female}, --sample-sex {m,y,male,Male,f,x,female,Female}, -g {m,y,male,Male,f,x,female,Female}, --gender {m,y,male,Male,f,x,female,Female} Specify the chromosomal sex of all given samples as male or female. [Default: guess each sample from coverage of X and Y chromosomes]. --no-shift-xy Don't adjust the X and Y chromosomes according to sample sex. -o FILENAME, --output FILENAME Output PDF file name. Plot aesthetics: -b, --by-bin Plot data x-coordinates by bin indices instead of genomic coordinates. All bins will be shown with equal width, no blank regions will be shown, and x-axis values indicate bin number (within chromosome) instead of genomic position. -d, --desaturate Tweak color saturation to focus on significant changes. -v, --vertical Plot heatmap with samples as X-axis (instead of Y-axis). --delimit-samples Add an horizontal delimitation line between each sample. -t TITLE, --title TITLE Plot title. [Default: Range if provided, otherwise none]