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TitanCNA a R/Bioconductor package for analyzing subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in whole genome and exome sequencing of tumours.
Ha, G., et al. (2014). TITAN: Inference of copy number architectures in clonal cell populations from tumour whole genome sequence data. Genome Research, 24: 1881-1893. (PMID: 25060187)
Dana-Farber Cancer Institute
contact: firstname.lastname@example.org or email@example.com
Date: May 13, 2017
Table of Contents
TitanCNA GitHub: https://github.com/gavinha/TitanCNA
KRONOS TITAN Workflow: https://github.com/MO-BCCRC/titan_workflow
Google Groups: https://groups.google.com/forum/#!forum/titancna
TitanCNA website: http://compbio.bccrc.ca/software/titan/
Publication in Genome Research: http://genome.cshlp.org/content/24/11/1881
(See NEWS for previous version notes)
TitanCNA version 1.15.0 changes
1) 10X Genomics analysis
- Please see scripts for instructions on running the 10X Genomics analysis.
2) New script to help select optimal solutions. Please see scripts/R_scripts
3) Added snakemake pipeline for entire TITAN workflow.
Please see scripts/snakemake.
4) New function
loadHaplotypeAlleleCounts(): loads input allele counts with phasing information
plotHaplotypeFraction(): results from 10X Genomics WGS data with phasing of haplotype blocks
5) Modified features (no changes for user-accessible functions)
- updateParameters: coordinate descent estimate of ploidy update uses previously estimated normal parameter from the same corodinate descent iteration ; leads to faster convergence
Install TitanCNA R package from github
From within R-3.3.2 or higher,
Install TitanCNA from Bioconductor
From within R-3.3.2 or higher,
Install other dependencies
Install the HMMcopy suite
Please follow instructions on the HMMcopy website http://compbio.bccrc.ca/software/hmmcopy/.
KRONOS TITAN Workflow
The easiest way to generate these files is by using the downloadable pipeline from https://github.com/MO-BCCRC/titan_workflow.
R scripts are provided to run the R component of the TITAN analysis using the TitanCNA R/Bioconductor package.
Please go to the scripts directory and look at the README there for more details.
Vignette in TitanCNA R package
The PDF of the vignette can be accessed from R
browseVignettes(package = "TitanCNA")
The path of the file can also be located using
pathToInstall <- system.file(package = "TitanCNA")
pathToPdf <- paste0(pathToInstall, "/int/doc/TitanCNA.pdf)
The example provided will reproduce Figure 1 in the manuscript. However, it will be slightly different because the example is only based on the analysis of chr2, not genome-wide.
TitanCNA was developed by Gavin Ha while in the laboratories of Sohrab Shah (firstname.lastname@example.org) and Sam Aparicio (email@example.com) at the Dept of Molecular Oncology, BC Cancer Agency, Vancouver, Canada.
Yikan Wang and Daniel Lai have contributed code and discussions to this project.
The KRONOS TITAN workflow was developed by Diljot Grewal (firstname.lastname@example.org) and Jafar Taghiyar (email@example.com).
HMMcopy was co-developed by Daniel Lai and Gavin Ha.
TitanCNA was inspired by existing methods including OncoSNP and PyClone
TitanCNA R code is open source and is R/Bioconductor package is under GPLv3. This applies to the v1.9.0 and all subsequent versions within and obtained from Bioconductor.
Users who are using TitanCNA earlier than v1.9.0 not for the purpose of academic research should contact firstname.lastname@example.org, email@example.com, and firstname.lastname@example.org to inquire about previous licensing.