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Python package and CLI for whole-genome duplication related analyses

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Documentation Status Hosted

Copyright (C) 2018 Arthur Zwaenepoel

VIB/UGent center for plant systems biology - Bioinformatics & evolutionary genomics group http:https://bioinformatics.psb.ugent.be/beg/

wgd - simple command line tools for the analysis of ancient whole-genome duplications

Installation

Python package and command line interface (CLI) for the analysis of whole-genome duplications (WGDs). Tested with Python3 on Linux. If you don't have python or pip installed a simple sudo apt-get install python3-pip should do.

To install, simply run

git clone https://github.com/arzwa/wgd.git
cd wgd
pip install --user .

Note that depending on your python installation and whether you're in a virtualenv, pip may default either to pip2 or pip3. If the above installation step fails, please try to use pip3 instead of pip.

For the command line interface, upon installation run

$ wgd

to get a list of the available commands. To get usage instructions for a command (e.g. ksd) run

$ wgd ksd --help

For external software requirements: please consult the relevant section in the docs

Quick start

The main aim of wgd is computing whole-paranome and one-vs.-one ortholog Ks distributions. For a whole-paranome distribution of a CDS sequence fasta file, the minimal commands are:

$ wgd dmd ath.cds.fasta
$ wgd ksd wgd_dmd/ath.cds.fasta.mcl ath.cds.fasta

For one-vs.one orthologs the minimal commands are

$ wgd dmd ath.cds.fasta vvi.cds.fasta
$ wgd ksd wgd_dmd/ath1000.fasta_vvi1000.fasta.rbh ath.cds.fasta vvi.cds.fasta

For more information and these methods and other tools implemented in wgd, please consult the docs.

NEW: diamond support

This has not been thoroughly tested yet, but may be of interest. Diamond is a sequence similarity search tool that is much faster than Blast and performance similar on other measures. If you have diamond installed, you can use wgd dmd for whole-paranome or one-vs.-one ortholog delineation, e.g.

$ wgd dmd ath.cds.fasta

for a whole-paranome, and

$ wgd dmd ath.cds.fasta vvi.cds.fasta

for one-vs.-one orthologs.

This is part of a new wgd version that is forthcoming. In the future this will replace wgd mcl. Please let me know of any bugs!

Singularity container

A singularity container is available for wgd, allowing all to use all tools in wgd except wgd syn, without having to install all required software on your system. To install Singularity follow the instructions here

If you have singulaity installed (and you're in the virtual machine when running on Windows or Mac), you can run the following to get the container

singularity pull --name wgd.simg shub:https://arzwa/wgd

Then you can use wgd as follows

singularity exec wgd.simg wgd <command>

Notes

Bug tracking: If the program crashes, exits unexpectedly or some unexpected results are obtained, please run it again with the --verbosity debug flag before the subcommand of interest (e.g. wgd --verbosity debug ksd gf.mcl cds.fasta). If the anomaly persists, please open an issue on this GitHub site.

Note on input data: while the input data is rather straightforward (a CDS fasta file will do for most analyses) it may be of interest that the wgd suite was extensively tested with data from the PLAZA platform, so for examples of the right input data formats (in particular CDS fasta files for sequence data and GFF files for structural annotation), please have a look there. It is generally advised not to include pipe characters (|) in your gene IDs, since these can have special meanings in certain parts of wgd.

Note on virtualenv: you can install wgd in a virtual environment (using virtualenv). If you would however encounter problems with running the executable directly (e.g. wgd --help doesn't work) you can circumvent this by directly calling the CLI, using python3 ./wgd_cli.py --help (assuming you are currently in the directory where you cloned wgd).

Citation

Please cite us at https://doi.org/10.1093/bioinformatics/bty915

Zwaenepoel, A., and Van de Peer, Y. wgd - simple command line tools for the analysis of ancient whole genome duplications. Bioinformatics., bty915, https://doi.org/10.1093/bioinformatics/bty915

For citation of the tools used in wgd, please consult the documentation at https://wgd.readthedocs.io/en/latest/index.html#citation.

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