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Phylogenetics

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Open Unknowns
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Cross-Domain Bridges
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Active Hypotheses

Cross-Domain Bridges

Bridge Phylogenetic generalised least squares (PGLS) corrects for the non- independence of closely related species by modelling trait covariance as proportional to shared branch length on the phylogenetic tree, bridging evolutionary biology to multivariate statistics through the variance- covariance structure of trait evolution under Brownian motion.

Fields: Evolutionary Biology, Statistics, Phylogenetics, Comparative Biology, Ecology

PROBLEM: Closely related species share evolutionary history โ€” a regression of body mass on metabolic rate across 100 mammal species treats data as 100 independent observations, but phylogenetic correl...

Bridge Phylogeography uses the coalescent theory from population genetics as a backward- time statistical model to date past population splits and migrations from present-day DNA sequences, with the molecular clock assumption providing the rate calibration that transforms branch lengths in mutations per site into years โ€” making evolutionary biology a direct application of stochastic process theory.

Fields: Evolutionary Biology, Statistics, Genetics, Phylogenetics

The coalescent (Kingman 1982) describes how a sample of gene copies traces back to a common ancestor, with coalescence events occurring at rate C(k,2)/N_e for k gene copies in a population of effectiv...

Bridge Phylogenetic trees are rooted Cayley trees โ€” graph-theoretic objects โ€” and maximum likelihood phylogenetics maximizes P(sequences|tree, model) over a combinatorially vast tree topology space of (2n-3)!! topologies, making exact search NP-hard and requiring heuristic graph algorithms from combinatorics.

Fields: Mathematics, Graph Theory, Combinatorics, Biology, Phylogenetics, Evolutionary Biology

A rooted bifurcating phylogenetic tree for n taxa is a Cayley tree โ€” a graph with n leaves, n-1 internal nodes, and 2n-2 edges, with the property that each internal node has exactly 3 incident edges (...

Open Unknowns (1)

Unknown What is the best method for correcting long-branch attraction (LBA) artefacts in maximum likelihood and Bayesian phylogenetic inference, and when do model violations (rate heterogeneity, compositional heterogeneity, saturation) produce systematic biases that cannot be corrected by more complex substitution models? u-phylogenetic-placement-long-branch-attraction-correction

Active Hypotheses

Hypothesis GTR+Gamma+I substitution models are inadequate for estimating deep Metazoan divergence times because they cannot account for compositional heterogeneity and long-branch saturation, causing systematic 10-30% underestimation of Cambrian and pre-Cambrian divergence dates compared to CAT+GTR non-homogeneous models. medium

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