Finding phylogeny-aware and biologically meaningful averages of metagenomic samples: L2UniFrac.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37387190.
- Also identified by DOI 10.1093/bioinformatics/btad238 and PMC identifier 10311324.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Metagenomic samples have high spatiotemporal variability. Hence, it is useful to summarize and characterize the microbial makeup of a given environment in a way that is biologically reasonable and interpretable. The UniFrac metric has been a robust and widely used metric for measuring the variability between metagenomic samples. We propose that the characterization of metagenomic environments can be improved by finding the average, a.k.a. the barycenter, among the samples with respect to the UniFrac distance. However, it is possible that such a UniFrac-average includes negative entries, making it no longer a valid representation of a metagenomic community. To overcome this intrinsic issue, we propose a special version of the UniFrac metric, termed L2UniFrac, which inherits the phylogenetic nature of the traditional UniFrac and with respect to which one can easily compute the average, producing biologically meaningful environment-specific "representative samples." We demonstrate the usefulness of such representative samples as well as the extended usage of L2UniFrac in efficient clustering of metagenomic samples, and provide mathematical characterizations and proofs to the desired properties of L2UniFrac. A prototype implementation is provided at https://github.com/KoslickiLab/L2-UniFrac.git. All figures, data, and analysis can be reproduced at https://github.com/KoslickiLab/L2-UniFrac-Paper.
Medical subject headings
- Metagenome
- Metagenomics