Evidence map›Paper›PMID 42891310›Full record

ArticleBioinformatics advances2026

TSLC: differential abundance analysis method for identifying biologically relevant known microbes.

Robert Beblavy, Cynthia L Monaco, Cassandra E Newkirk, Jin Xiao, Michael B Sohn

Abstract read
In one paragraph

Article in Bioinformatics advances, 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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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

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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

5 authors.

Robert BeblavyBiostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY 14642, United States.
Cynthia L MonacoMicrobiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, United States.
Cassandra E NewkirkMicrobiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, United States.
Jin XiaoEastman Institute for Oral Health, University of Rochester Medical Center, Rochester, NY 14620, United States.
Michael B SohnBiostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY 14642, United States.ORCID https://orcid.org/0000-0002-4981-8351

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
Understand biological factors underlying early childhood caries disparity from the oral microbiome in early infancyR01DE031025 · NIDCR · UNIVERSITY OF ROCHESTER · PI STEVEN R. GILL, Tongtong Wu · 2022 to 2026
$3.9M
Influence of the Cervicovaginal Phageome on Health and Disease in Women Living with HIV.K08AI181643 · NIAID · UNIVERSITY OF ROCHESTER · PI Cynthia L. Monaco · 2024 to 2026
$589k
NCATS NIH HHS UL1 TR002001NIAID NIH HHS K08 AI181643NIDCR NIH HHS R01 DE031025
6 · The paper itself

Abstract

Motivation: Identifying biologically relevant microbes is a crucial task in human microbiome studies. Numerous computational and statistical methods have been proposed for this task. However, most existing methods are based solely on taxonomic information, even when whole-metagenome sequencing data are available, and thus cannot account for the fact that different microbes can perform the same or similar functions (known as Results: To address the issues with existing methods, we propose a two-stage procedure: (i) determining differentially abundant functions between groups; and then (ii) determining microbes significantly associated with each identified differentially abundant function. This procedure involves Availability and implementation: An R package for the proposed method is available at https://github.com/rgbeblavy/TSLC.

Identifiers

PMID42891310
PMCPMC13674353

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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.