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barbieQ: an R software package for analysing barcode count data from clonal tracking experiments
Liyang Fei1,2, Jovana Maksimovic1,2, Alicia Oshlack1,2
1Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
Bioinformatics (Oxford, England)
|June 16, 2026
Summary
A new R package, barbieQ, offers a generalized workflow for analyzing DNA barcode count data from single-cell lineage tracing experiments. It provides robust statistical tests and quality control to improve clonal tracking analysis across diverse samples.
Area of Science:
- * Computational Biology
- * Genomics
- * Bioinformatics
Background:
- * Single-cell lineage tracing utilizes DNA barcodes to track cell populations and their progeny.
- * Current analysis of barcode count data lacks a standardized, robust workflow, often relying on bespoke methods.
- * A generalized approach is needed for preprocessing and statistical analysis of barcode count data.
Purpose of the Study:
- * To introduce barbieQ, a Bioconductor R package for analyzing barcode count data.
- * To provide data-driven quality control, filtering, and visualization tools.
- * To implement robust statistical tests for differential barcode analysis.
Main Methods:
- * Development of the barbieQ R package available on Bioconductor.
- * Implementation of two statistical tests: differential barcode proportion and differential barcode occurrence.
- * Utilizing regression models to handle complex experimental designs and account for sample variability.
Main Results:
- * barbieQ offers data-driven quality control and filtering capabilities.
- * The package includes extensive visualizations for barcode count data.
- * Validated statistical tests demonstrate appropriate statistical properties (size and power) and outperform existing methods.
Conclusions:
- * barbieQ provides a generalized and robust workflow for analyzing single-cell lineage tracing barcode data.
- * The package enhances the statistical rigor and analytical power for clonal tracking studies.
- * barbieQ facilitates more reliable comparisons of clonal composition across different experimental groups.

