Evidence map›Paper›PMID 41959051›Full record

ArticlebioRxiv : the preprint server for biology2026

A Multi-Omics Processing Pipeline (MOPP) for Extracting Taxonomic and Functional Insights from Metaribosome Profiling (metaRibo-Seq) data.

Yuhan Weng, Oriane Moyne, Corinn Walker, Eli Haddad, Chloe Lieng, Loryn Chin, Gibraan Rahman, Daniel McDonald, Rob Knight, Karsten Zengler

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.

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

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

10 authors.

Yuhan WengBioinformatics and Systems Biology Program, University of California San Diego, La Jolla, CA, USA.ORCID 0009-0005-3453-1402
Oriane MoyneDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Corinn WalkerDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Eli HaddadDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.ORCID 0009-0000-1536-9992
Chloe LiengDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.ORCID 0009-0009-9424-0016
Loryn ChinHuman Microbiome Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Gibraan RahmanDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-8843-0229
Daniel McDonaldDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Rob KnightDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Karsten ZenglerDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.

Funding

Defining the Quantitative Functional Mechanisms that Underly Gut Microbiome-Diet Interactions Contributing to Human Energy BalanceR01DK140328 · NIDDK · ADVENTHEALTH ORLANDO · PI Karen Davidowitz Corbin, Karsten B Zengler · 2024 to 2026
$1.8M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
NIDDK NIH HHS R01 DK140328NIH HHS S10 OD026929
6 · The paper itself

Abstract

Metaribosome profiling (metaRibo-Seq) enables genome-wide measurement of translation across complex microbial communities by sequencing ribosome-protected mRNA fragments, but the short length of these footprints creates substantial nonspecific mapping against large reference genome collections, leading to spurious taxonomic and functional assignments. Here we present MOPP (Multi-Omics Processing Pipeline), a modular reference-based workflow that denoises metaRibo-Seq data by leveraging matched metagenomic coverage breadth to identify genomes likely to be truly present in a sample before aligning metatranslatomic and optional metatranscriptomic reads. MOPP generates taxon-by-gene count tables across genomic, transcriptional and translational layers, enabling integrated downstream analyses of microbial function. We evaluated MOPP using a defined 79-member synthetic human gut community profiled by metagenomics and metaRibo-Seq. Coverage breadth filtering markedly improved detection accuracy relative to a standard baseline workflow, with performance remaining robust across a broad intermediate threshold range and peaking at 92-95% coverage breadth. At a 92% threshold, MOPP reduced the number of distinct detected operational genomic units by 99.4% while retaining 87.8% of aligned metaRibo-Seq reads on average, and increased the F1 score from 0.02 to 0.61. Residual false positives were predominantly attributable to genomes with extremely high nucleotide similarity to true community members, whereas false negatives were enriched among low-abundance taxa, indicating that remaining errors are driven primarily by biological similarity and detection limits rather than widespread nonspecific mapping. Together, these results establish MOPP as a high-throughput workflow for robust processing of metaRibo-Seq in the context of matched metagenomics and position it as a scalable framework for integrated taxonomic and functional analysis of microbial communities across genomic, transcriptional and translational layers.

Identifiers

PMID41959051
PMCPMC13061286

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.