CaPSID: Computational Pathogen Sequence Identification
Project description
CaPSID
CaPSID (Computational Pathogen Sequence IDentification) is a comprehensive open source platform which integrates a high-performance computational pipeline for pathogen sequence identification and characterization in human genomes and transcriptomes together with a scalable results database and a user-friendly web-based software application for managing, querying and visualizing results.
Project Leader Vincent Ferretti
Development Team Ivan Borozan, Philippe Laflamme, Shane Wilson
Downloading and using CaPSID is free, if you use CaPSID or its code in your work please acknowledge CaPSID by referring to its GitHub homepage https://github.com/capsid. This is important for us since obtaining grants is one significant way to fund planning and implementation for our project. Also if you find CaPSID useful in your research feel free to let us know.
Getting Started
You will need a MongoDB database, a Python 2.7 installation and a Java Web Server. For more details, read the wiki:
License and Copyright
Licensed under the GNU General Public License, Version 3.0. See LICENSE for more details.
Copyright 2011 The Ontario Institute for Cancer Research.
Acknowledgement
This project is supported by the Ontario Institute for Cancer Research (OICR) through funding provided by the government of Ontario, Canada.
News
1.4.0
Release date: 1 June 2012
Adds statistics while they are being run rather than all at the end
Saves unique id for genes as uid
1.3.0
Release date: 28 Feb 2012
Adds a new field in mapped for AS tag
Links mapped genes to NCBI page
Uses max sample coverage for project max coverage
Adds timer to wait for file collapsing to finish when intersecting
Using a path/to/file input no longer breaks intersecting
1.2.6
Release date: 6 Feb 2012
Subtraction filters out unmapped when building mapped reads
1.2
Release date: 20 Jan 2012
Utility to create FastQ files from unmapped reads
Utility to return intersection of FastQ files
Utility to return filter FastQ files
Added mapq threshold flag to subtraction
Gbloader can now load bacteria and fungal genomes
Saves genome sequences to database using GridFS
Reduced memory footprint when calculating statistics
use subprocesses instead of os.system
mapq scores filter needs to include 0 <= mapq <=3 due to multiple mapping reads
1.1
Release date: 25 Nov 2011
Adds support for pair-end reads
1.0.1
Release date: 19 Oct 2011
Added support for MongoDB authentication
1.0
Release date: 12 Oct 2011
Initial release
Project details
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