Evidence map›Paper›PMID 41959466›Full record

ArticlebioRxiv : the preprint server for biology2026

Leveraging spectrum of graph sheaf Laplacian as a genome-architecture-aware measure of microbiome diversity.

Nicolae Sapoval, Todd J Treangen, Luay Nakhleh

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Nicolae SapovalDepartment of Computer Science, Rice University.ORCID 0000-0002-0736-5075
Todd J TreangenDepartment of Computer Science, Rice University.ORCID 0000-0002-3760-564X
Luay NakhlehDepartment of Computer Science, Rice University.ORCID 0000-0003-3288-6769

Funding

Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogenP01AI152999 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HAAG, ANTHONY · 2020 to 2025
$12.0M
NIAID NIH HHS P01 AI152999
6 · The paper itself

Abstract

Motivation: Measures of microbial diversity that can be derived directly from metagenomic sequencing data offer a valuable summary view of the underlying complex systems. Prior work has shown that both taxonomic composition and abundances that are captured by standard diversity measures (e.g., Shannon entropy), and structural variation within the metagenome due to gene duplications, losses and horizontal transfers (HGT), can correlate with the host's health. However, there are no diversity measures available that simultaneously account for the genome architecture and taxonomic composition within the sample. Thus, in this work we propose the spectral energy of a graph sheaf Laplacian as such a measure, and justify its applicability through a simulation study and analysis of biological data. Results: First, we describe a theoretical framework that allows us to combine the features of genome graphs with the taxonomic data. Then, we explore the sensitivity of the proposed diversity measure to genome rearrangements and HGT events in a simulation study. Finally, we explore applicability of our proposed measure to characterization of diversity of human gut metagenomes. We find our proposed measure to offer better discrimination between healthy controls and inflammatory bowel disease (IBD) patients' samples ( Availability and Implementation: https://github.com/nsapoval/bd-gsl.

Indexed as

genome graphshorizontal gene transfermetagenomicsmicrobiome diversitystructural variants

Identifiers

PMID41959466
PMCPMC13060994

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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.