pyGenomeTracks 3.4

Command-line tool to make beautiful and reproducible genome browser snapshots

pyGenomeTracks

Standalone program and library to plot beautiful genome browser tracks

pyGenomeTracks aims to produce high-quality genome browser tracks that are highly customizable. Currently, it is possible to plot:

• bigwig
• bed/gtf (many options)
• bedgraph
• epilogos
• narrow peaks
• links (represented as arcs)
• Hi-C matrices

pyGenomeTracks can make plots with or without Hi-C data. The following is an example output of pyGenomeTracks from Ramírez et al. 2017

Table of content

• Installation
• Usage
• Citation
• Documentation
• External users

Installation

pyGenomeTracks works with python >=3.6.

Currently, the best way to install pyGenomeTracks is with anaconda

$ conda install -c bioconda -c conda-forge pygenometracks

Also, pyGenomeTracks can be installed using pip

$ pip install pyGenomeTracks

If the latest version wants to be installed use:

$ pip install  git+https://github.com/deeptools/pyGenomeTracks.git

Usage

To run pyGenomeTracks a configuration file describing the tracks is required. The easiest way to create this file is using the program make_tracks_file which creates a configuration file with defaults that can be easily changed. The format is:

$ make_tracks_file --trackFiles <file1.bed> <file2.bw> ... -o tracks.ini

make_tracks_file uses the file ending to guess the file type.

Then, a region can be plotted using:

$ pyGenomeTracks --tracks tracks.ini --region chr2:10,000,000-11,000,000 --outFileName nice_image.pdf

The ending --outFileName defines the image format. If .pdf is used, then the resulting image is a pdf. The options are pdf, png and svg.

Description of other possible arguments:

optional arguments:
  -h, --help            show this help message and exit
  --tracks TRACKS       File containing the instructions to plot the tracks.
                        The tracks.ini file can be genarated using the
                        `make_tracks_file` program.
  --region REGION       Region to plot, the format is chr:start-end
  --BED BED             Instead of a region, a file containing the regions to
                        plot, in BED format, can be given. If this is the
                        case, multiple files will be created using a prefix
                        the value of --outFileName
  --width WIDTH         figure width in centimeters (default is 40)
  --height HEIGHT       Figure height in centimeters. If not given, the figure
                        height is computed based on the heights of the tracks.
                        If given, the track height are proportionally scaled
                        to match the desired figure height.
  --title TITLE, -t TITLE
                        Plot title
  --outFileName OUTFILENAME, -out OUTFILENAME
                        File name to save the image, file prefix in case
                        multiple images are stored
  --fontSize FONTSIZE   Font size for the labels of the plot (default is 0.3 *
                        figure width)
  --dpi DPI             Resolution for the image in case the ouput is a raster
                        graphics image (e.g png, jpg) (default is 72)
  --trackLabelFraction TRACKLABELFRACTION
                        By default the space dedicated to the track labels is
                        0.05 of the plot width. This fraction can be changed
                        with this parameter if needed.
  --trackLabelHAlign {left,right,center}
                        By default, the horizontal alignment of the track
                        labels is left. This alignemnt can be changed to right
                        or center.
  --decreasingXAxis     By default, the x-axis is increasing. Use this option
                        if you want to see all tracks with a decreasing
                        x-axis.
  --version             show program's version number and exit

Citation

If you use pyGenomeTracks in your analysis, you can cite the following paper :

Fidel Ramírez, Vivek Bhardwaj, Laura Arrigoni, Kin Chung Lam, Björn A. Grüning, José Villaveces, Bianca Habermann, Asifa Akhtar & Thomas Manke. High-resolution TADs reveal DNA sequences underlying genome organization in flies. Nature Communications (2018) doi:10.1038/s41467-017-02525-w

Documentation

Our documentation provide examples, as well as the full list of possible parameters and guidelines for developers who would like to add a new track type.

External users

• CoolBox is an interactive genomic data explorer for Jupyter Notebooks
• Galaxy integration offers a graphical user-interface to create PGT plots. It is also possible to include PGT into workflows and automatic pipelines.