Copyright 2012, 2013, 2014, 2015 Brown University, Providence, RI. All Rights Reserved Permission to use, copy, modify, and distribute this software and its documentation for any purpose other than its incorporation into a commercial product is hereby granted without fee, provided that the above copyright notice appear in all copies and that both that copyright notice and this permission notice appear in supporting documentation, and that the name of Brown University not be used in advertising or publicity pertaining to distribution of the software without specific, written prior permission. BROWN UNIVERSITY DISCLAIMS ALL WARRANTIES WITH REGARD TO THIS SOFTWARE, INCLUDING ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR ANY PARTICULAR PURPOSE. IN NO EVENT SHALL BROWN UNIVERSITY BE LIABLE FOR ANY SPECIAL, INDIRECT OR CONSEQUENTIAL DAMAGES OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS OF USE, DATA OR PROFITS, WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE OR OTHER TORTIOUS ACTION, ARISING OUT OF OR IN CONNECTION WITH THE USE OR PERFORMANCE OF THIS SOFTWARE. http://cs.brown.edu/people/braphael/software.html README file for Tumor Heterogeneity Analysis (THetA) Software that estimates tumor purity and clonal/subclonal copy number aberrations directly from high-throughput DNA sequencing data. If you use this software in your research, please cite: L. Oesper, G. Satas, B.J. Raphael. (2014) Quantifying Tumor Heterogeneity in Whole-Genome and Whole-Exome Sequencing Data. Bioinformatics. (In Press). L. Oesper, A. Mahmoody, B.J. Raphael. (2013) THetA: Inferring intra-tumor heterogeneity from high-throughput DNA sequencing data. Genome Biology. 14:R80. contact: layla@cs.brown.edu braphael@cs.brown.edu Beta Version: 0.7 Version data: October, 2015 WEBSITE: http://compbio.cs.brown.edu/software/ http://compbio.cs.brown.edu/projects/theta/ SUMMARY======================================================================== This software is for estimating tumor purity (fraction of non-cancerous cells) and clonal/subclonal copy number aberrations from high-throughput DNA sequencing data for a tumor normal pair. CONTENTS ====================================================================== (i) Documentation (in doc/ subdirectory): * Manual; MANUAL.txt - A complete description of how to install/run the software. * Release Notes; RELEASE_NOTES.txt - List of changes between different versions. * License; LICENSE.txt - The complete license that goes with the software. (ii) Software (Main code in python/ Additional code in java/src/, jarfiles, and matlab/ subdirectories): * Source code in python/, java/src and matlab/ (iii) Executables (in bin/ subdirectory ): * Executables for compiling and running code (iv) Example (in example/ subdirectory) * Example input/output files (v) Data (in data/ subdirectory) * Useful data files for use with whole-exome sequencing data