Evidence map›Paper›PMID 40774815›Full record

ArticleGenome research2025

ERC2.0 evolutionary rate covariation update improves inference of functional interactions across large phylogenies.

Jordan H Little, Guillermo Hoffmann Meyer, Aakash Grover, Alex Michael Francette, Raghavendran Partha, Karen M Arndt, Martin Smith, Nathan Clark, Maria Chikina

Abstract read
In one paragraph

Article in Genome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jordan H LittleDepartment of Human Genetics, University of Utah, Salt Lake City, Utah 84112, USA.ORCID 0000-0002-8590-9357
Guillermo Hoffmann MeyerDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.ORCID 0009-0009-8127-038X
Aakash GroverDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.ORCID 0009-0009-0211-7118
Alex Michael FrancetteDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.ORCID 0000-0003-1145-5847
Raghavendran ParthaDepartment of Computational and Systems Biology, University of Pittsburgh, Pennsylvania 15213, USA.ORCID 0000-0002-7900-4375
Karen M ArndtDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.ORCID 0000-0003-1320-9957
Martin SmithDepartment of Earth Sciences, University of Durham, Durham DH1 3LE, United Kingdom.ORCID 0000-0001-5660-1727
Nathan ClarkDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA; nclark@pitt.edu.ORCID 0000-0003-0006-8374
Maria ChikinaDepartment of Computational and Systems Biology, University of Pittsburgh, Pennsylvania 15213, USA.ORCID 0000-0003-2550-5403

Funding

Title: Functional Annotation of Genomes via Phenotypic Convergence within Large Multi-species AlignmentsR01HG009299 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Maria D Chikina, Nathaniel L Clark · 2017 to 2026
$4.1M
Mechanisms that Couple Chromatin Modifications to TranscriptionR35GM141964 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAREN M ARNDT · 2021 to 2026
$2.8M
NHGRI NIH HHS R01 HG009299NIGMS NIH HHS R35 GM141964
6 · The paper itself

Abstract

Evolutionary rate covariation (ERC) is an established comparative genomics method that identifies sets of genes sharing patterns of sequence evolution, which suggests shared function. Whereas many functional predictions of ERC have been empirically validated, its predictive power has hitherto been limited by its inability to tackle the large numbers of species in contemporary comparative genomics data sets. This study introduces ERC2.0, an enhanced methodology for studying ERC across phylogenies with hundreds of species and tens of thousands of genes. ERC2.0 improves upon previous iterations of ERC in algorithm speed, normalizing for heteroskedasticity, and normalizing correlations via Fisher transformations. These improvements have resulted in greater statistical power to predict biological function. In exemplar yeast and mammalian data sets, we demonstrate that the predictive power of ERC2.0 is improved relative to the previous method, ERC1.0, and that further improvements are obtained by using larger yeast and mammalian phylogenies. We attribute the improvements to both the larger data sets and improved rate normalization. We demonstrate that ERC2.0 has high predictive accuracy for known annotations and can predict the functions of genes in nonmodel systems. Our findings underscore the potential for ERC2.0 to be used as a single-pass computational tool in candidate gene screening and functional predictions.

Indexed as

Evolution, MolecularGenomicsPhylogenySoftwareAlgorithmsAnimalsHumansMammalsSaccharomyces cerevisiae

Identifiers

PMID40774815
PMCPMC12400958

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.