LSX
LSX reduces lineage rate heterogeneity in multi-gene phylogeny inference by implementing LS³ and LS⁴ subsampling algorithms that remove fast- and extremely slow-evolving sequences to improve phylogenetic signal.
Key Features:
- LS³ algorithm: Identifies gene-specific subsets by removing fast-evolving sequences to obtain relatively homogeneous evolutionary rates, minimizing non-phylogenetic noise while preserving phylogenetic signal.
- LS⁴ algorithm: Detects both fast-evolving and extremely slow-evolving sequences to enable less stringent subsampling in datasets containing very slow-evolving lineages.
- Data subsampling strategy: Performs sequence removal/subselection across genes to reduce lineage rate heterogeneity in multi-gene datasets.
- Reprogrammed lineage rate calculations: Revises LS³ implementation to improve lineage rate calculations compared with the previous implementation.
- R implementation: Implemented as an R script.
- Scalability: Applicable to multi-gene sequence datasets of any size.
Scientific Applications:
- Multi-gene phylogeny inference: Reduces bias from lineage rate heterogeneity to improve accuracy of phylogenetic tree estimation.
- Resolution of contentious nodes: Enhances resolution of difficult or disputed phylogenetic relationships by minimizing non-phylogenetic signal.
- Empirical phylogenetic analyses: Applied to a catfish phylogeny dataset exhibiting high lineage rate heterogeneity to improve inference.
Methodology:
Implements LS³ and LS⁴ algorithms for gene-specific sequence subsampling (LS³ removes fast-evolving sequences; LS⁴ detects fast- and extremely slow-evolving sequences) and its performance has been validated via simulations and empirical studies.
Topics
Details
- License:
- GPL-3.0
- Tool Type:
- library
- Programming Languages:
- R, Bash
- Added:
- 11/14/2019
- Last Updated:
- 12/22/2020
Operations
Publications
Rivera-Rivera CJ, Montoya-Burgos JI. LSX: automated reduction of gene-specific lineage evolutionary rate heterogeneity for multi-gene phylogeny inference. BMC Bioinformatics. 2019;20(1). doi:10.1186/s12859-019-3020-1. PMID:31409290. PMCID:PMC6693147.