Hello everyone,
I have previously worked with gene tree/species tree evolution tools but not tumor evolution so if it looks like a silly question, I beg your pardon.
I have variant calling data (using Mutect and VarScan) for whole-exome sequencing data. In the review paper, such as http://sysbio.oxfordjournals.org/content/64/1/e1, the authors say that, for instance, for PyClone, Phylosub and SciClone, the input data is single nucleotide variant (SNV). When I check, for instance, in test data in PyClone, it has a nicely formatted input file which is used to generate the output.
I am wondering if someone has worked with any pipeline for phylogenetic tree reconstruction using "any" of tumor evolution software? I would be grateful if you can share your experience (and, if possible, the steps).
Thanks in advance
You are asking for an approach to running multiple software packages, or something different?
I am interested in sub-clonal evolution in primary tumor and secondary (metastasis) sites using one or more phylogenetic tools.