Wellcome Trust Centre for Human Genetics

chaos
Annotation, analysis and visualization of variants from high-throughput sequencing experiments

 

Introduction

CHAoS is a Perl-based system for annotation of variants identified in high-throughput sequencing experiments developed at the Wellcome Trust Centre for Human Genetics (WTCHG).

Functionality includes annotation of variants with information relating to population genetics, known transcripts, positional records, and sequence motif-based prediction. In addition, annotated variants can be summarized and extracted to facilitate downstream analysis.

There is also basic support for gene-based biological annotation, and eventually will include tools for variant and genotype analysis and visualization.


Download

CHAoS releases can be downloaded here


Documentation

Installation instructions are included as part of the Chaos distribution (README).

Overview of usage and features can be obtained here or by running Chaos without any arguments after installation


Supplemental annotation data

Gene function annotation filesgene_annot.tar.gzupdated 6 FEB 2012
ENCODE regulatory data filesreg/updated 6 FEB 2012



Contact

Kyle Gaulton < kgaulton@gmail.com >
Manuel Rivas < rivas@broadinstitute.org >

 
 
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