In caravagnalab/lineaGT: lineaGT

knitr::opts_chunk$set(
  collapse = TRUE,
  comment = "#>",
  fig.path = "man/figures/README-",
  out.width = "100%"
)

lineaGT

This package implements algorithm to determine lineage inference for gene therapy assays based on insertion sites, accounting also for somatic mutations accumulation. More specifically, starting from coverage values of ISs identified in a gene therapy assays and associated somatic mutations, lineaGT can:

• cluster ISs from the observed multi-lineage longitudinal coverage to identify populations of cells originated from the same Haematopoietic Stem Cell and estimate their abundances in the sample;

• cluster somatic mutations from the observed multi-lineage longitudinal variant allele frequency within each clone, to identify subpopulations;

• infer population genetics parameters, i.e., growth rates, for each population supporting the exponential and logistic growth models and selecting the optimal one.

This R package provides an R interface for the Python algorithms developed in the pyLineaGT package, which uses the Pyro probabilistic programming language to infer lineage histories.

Citation

If you use lineaGT, please cite:

• E. Buscaroli, S. Milite, R. Bergamin, N. Calonaci, F. Gazzo, A. Calabria, G. Caravagna. Bayesian multi-lineage tracing in gene therapy assays. In preparation.

Help and support

Installation

You can install the released version of lineaGT from GitHub with:

# install.packages("devtools")
devtools::install_github("caravagnalab/lineaGT")

---

Copyright and contacts

Elena Buscaroli, Giulio Caravagna. Cancer Data Science (CDS) Laboratory, University of Trieste, Italy.

caravagnalab/lineaGT documentation built on June 13, 2025, 6:01 p.m.