Prediction of copy number alterations and structural variants using deep-sequencing data

 FREEC-SV HOWTOs:

  1. Install all components

  2. Run FREEC-SV

  3. Visualize in Circos

 Contact:

Valentina Boeva: FREEC@curie.fr

phone: +33.1.56.24.69.88

 Distributions:

FREEC and SVDetect are free software; you can redistribute it and/or modify it under the terms of the GNU General Public License and GNU Public License correspondingly as published by the Free Software Foundation (www.fsf.org).

 Installation:

  • Download and install FREEC here
  • Download and install SVDetect here
  • Download scripts to combine the output of the two programs here

 Run FREEC-SV

Type perl crossFreecSVDetect.pl in the command line to get the list of functions

 Translate FREEC's output into Bed or Circos formats

To translate an output of FREEC to a Bed file (so to view it in the UCSC Genome Browser) or to the Circos format, use these scripts: freec2bed.pl and freec2circos.pl


Last modified: Jul 14 2011