ArticlePloS one2012
PHYRN: a robust method for phylogenetic analysis of highly divergent sequences.
Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- A new lineage of segmented RNA viruses infecting animals.Virus evolution · 2020Article
- Genomic Characterization of Cyanophage vB_AphaS-CL131 Infecting Filamentous Diazotrophic CyanobacteriumApplied and environmental microbiology · 2019Article
- GenFamClust: an accurate, synteny-aware and reliable homology inference algorithm.BMC evolutionary biology · 2016Article
- Sequence analysis reveals a conserved extension in the capping enzyme of the alphavirus supergroup, and a homologous domain in nodaviruses.Biology direct · 2015Article
- Domain organization of DNase from Thioalkalivibrio sp. provides insights into retention of activity in high salt environments.Frontiers in microbiology · 2015Article
- Molecular dynamic simulations reveal the structural determinants of Fatty Acid binding to oxy-myoglobin.PloS one · 2015Article
- Reevaluation of the evolutionary events within recA/RAD51 phylogeny.BMC genomics · 2013Article
- Quantitative synteny scoring improves homology inference and partitioning of gene families.BMC bioinformatics · 2013Article
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Authors and funding
15 authors.
Funding
Abstract
Both multiple sequence alignment and phylogenetic analysis are problematic in the "twilight zone" of sequence similarity (≤ 25% amino acid identity). Herein we explore the accuracy of phylogenetic inference at extreme sequence divergence using a variety of simulated data sets. We evaluate four leading multiple sequence alignment (MSA) methods (MAFFT, T-COFFEE, CLUSTAL, and MUSCLE) and six commonly used programs of tree estimation (Distance-based: Neighbor-Joining; Character-based: PhyML, RAxML, GARLI, Maximum Parsimony, and Bayesian) against a novel MSA-independent method (PHYRN) described here. Strikingly, at "midnight zone" genetic distances (~7% pairwise identity and 4.0 gaps per position), PHYRN returns high-resolution phylogenies that outperform traditional approaches. We reason this is due to PHRYN's capability to amplify informative positions, even at the most extreme levels of sequence divergence. We also assess the applicability of the PHYRN algorithm for inferring deep evolutionary relationships in the divergent DANGER protein superfamily, for which PHYRN infers a more robust tree compared to MSA-based approaches. Taken together, these results demonstrate that PHYRN represents a powerful mechanism for mapping uncharted frontiers in highly divergent protein sequence data sets.
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Registered trials
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