Evidence map›Paper›PMID 39803481›Full record

ArticlebioRxiv : the preprint server for biology2025

A data-driven modeling framework for mapping genotypes to synthetic microbial community functions.

Yili Qian, Sarvesh D Menon, Nick Quinn-Bohmann, Sean M Gibbons, Ophelia S Venturelli

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Yili QianDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Sarvesh D MenonDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Nick Quinn-BohmannInstitute of Systems Biology, Seattle, WA 98109, USA.
Sean M GibbonsInstitute of Systems Biology, Seattle, WA 98109, USA.ORCID 0000-0002-8724-7916
Ophelia S VenturelliDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0003-2200-1963

Funding

CyberGut: towards personalized human-microbiome metabolic modeling for precision health and nutritionR01DK133468 · NIDDK · INSTITUTE FOR SYSTEMS BIOLOGY · PI Sean Michael Gibbons · 2022 to 2026
$3.6M
Elucidating the molecular and ecological design principles of stability and assembly of the human gut microbiotaR35GM124774 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Ophelia Venturelli · 2017 to 2026
$2.9M
Model-guided design of next-generation bacterial therapeutics to treat cardiovascular diseaseR01EB030340 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI REY, FEDERICO E, ROMERO, PHILIP ANTHONY · 2020 to 2023
$2.8M
NIBIB NIH HHS R01 EB030340NIDDK NIH HHS R01 DK133468NIGMS NIH HHS R35 GM124774
6 · The paper itself

Abstract

Microbial communities play a central role in transforming environments across Earth, driving both physical and chemical changes. By harnessing these capabilities, synthetic microbial communities, assembled from the bottom up, offer valuable insights into the mechanisms that govern community functions. These communities can also be tailored to produce desired outcomes, such as the synthesis of health-related metabolites or nitrogen fixation to improve plant productivity. Widely used computational models predict synthetic community functions using species abundances as inputs, making it impossible to predict the effects of species not included in the training data. We bridge this gap using a data-driven community genotype function (dCGF) model. By lifting the representation of each species to a high-dimensional genetic feature space, dCGF learns a mapping from community genetic feature matrices to community functions. We demonstrate that dCGF can accurately predict communities in a fixed environmental context that are composed in part or entirely from new species with known genetic features. In addition, dCGF facilitates the identification of species roles for a community function and hypotheses about how specific genetic features influence community functions. In sum, dCGF provides a new data-driven avenue for modeling synthetic microbial communities using genetic information, which could empower model-driven design of microbial communities.

Identifiers

PMID39803481
PMCPMC11722394

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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.