| Literature DB >> 29927069 |
Camir Ricketts1,2, Victoria Popic3, Hosein Toosi4, Iman Hajirasouliha2,5.
Abstract
The reconstruction of cancer phylogeny trees and quantifying the evolution of the disease is a challenging task. LICHeE and BAMSE are two computational tools designed and implemented recently for this purpose. They both utilize estimated variant allele fraction of somatic mutations across multiple samples to infer the most likely cancer phylogenies. This unit provides extensive guidelines for installing and running both LICHeE and BAMSE.Entities:
Keywords: cancer phylogeny; deep sequencing; next-generation sequencing; somatic variations; tumor heterogeneity
Mesh:
Year: 2018 PMID: 29927069 PMCID: PMC6020047 DOI: 10.1002/cpbi.49
Source DB: PubMed Journal: Curr Protoc Bioinformatics ISSN: 1934-3396