Evidence map›Paper›PMID 41436922›Full record

ArticleBMC bioinformatics2025

Phylograd: fast column-specific calculation of substitution model gradients.

Benjamin Lieser, Georgy Belousov, Johannes Söding

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Benjamin LieserQuantitative and Computational Biology, Max Planck Institute for Multidisciplinary Sciences, Am Faßberg 11, Göttingen, 37077, Germany. benjamin.lieser@mpinat.mpg.de.
Georgy BelousovQuantitative and Computational Biology, Max Planck Institute for Multidisciplinary Sciences, Am Faßberg 11, Göttingen, 37077, Germany.
Johannes SödingQuantitative and Computational Biology, Max Planck Institute for Multidisciplinary Sciences, Am Faßberg 11, Göttingen, 37077, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost popular tools for reconstructing phylogenetic trees from multiple sequence alignments use a model of molecular evolution in which a single substitution matrix or a small set of fixed matrices are shared between all columns. Models with column-specific rate matrices can in principle be fit by automatic differentiation methods, but in practice the heavy computational burden associated with computing the gradients of the many matrix exponentials has hindered exploration of such models. IMPLEMENTATION: Here, we present a highly efficient approach for reverse-mode differentiation of the log likelihood computed with Felsenstein's algorithm under any time-reversible substitution model. PhyloGrad is implemented in Rust and has Python bindings to easily combine it with automatic differentiation tools.

resultsDepending on the tree size, PhyloGrad is 30-100 times faster than automatic differentiation in Pytorch and uses 10-100 times less memory. Even in the task of fitting one global model it is still at least 10 times faster than IQ-TREE3. PhyloGrad accelerates current model optimizations and enables the field to easily explore and implement novel site-specific models.

Indexed as

AlgorithmsComputational BiologyModels, GeneticPhylogenySequence AlignmentSoftwareEvolution, MolecularFelsensteinPhylogenyReverse-mode differentiationSite-specific models

Identifiers

PMID41436922
PMCPMC12836810

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.