Evidence map›Paper›PMID 40328944›Full record

ArticleNature microbiology2025

Longitudinal profiling of low-abundance strains in microbiomes with ChronoStrain.

Younhun Kim, Colin J Worby, Sawal Acharya, Lucas R van Dijk, Daniel Alfonsetti, Zackary Gromko, Philippe N Azimzadeh, Karen W Dodson, Georg K Gerber, Scott J Hultgren and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Nature microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Younhun KimDepartment of Mathematics, Massachusetts Institute of Technology, Cambridge, MA, USA.
Colin J WorbyBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-9132-7249
Sawal AcharyaDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Lucas R van DijkBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Daniel AlfonsettiComputer Science and AI Lab, Massachusetts Institute of Technology, Cambridge, MA, USA.
Zackary GromkoComputer Science and AI Lab, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-1692-370X
Philippe N AzimzadehDepartment of Molecular Microbiology and Center for Women's Infectious Disease Research, Washington University School of Medicine, St Louis, MO, USA.
Karen W DodsonDepartment of Molecular Microbiology and Center for Women's Infectious Disease Research, Washington University School of Medicine, St Louis, MO, USA.
Georg K GerberDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9149-5509
Scott J HultgrenDepartment of Molecular Microbiology and Center for Women's Infectious Disease Research, Washington University School of Medicine, St Louis, MO, USA.ORCID http://orcid.org/0000-0001-8785-564X
Ashlee M EarlBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-7857-9145
Bonnie BergerDepartment of Mathematics, Massachusetts Institute of Technology, Cambridge, MA, USA. bab@mit.edu.ORCID http://orcid.org/0000-0002-2724-7228
Travis E GibsonDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA. tegibson@bwh.harvard.edu.ORCID http://orcid.org/0000-0003-0320-8010

Funding

Viral Genomics: evolution, spread, and host interactionsU19AI110818 · NIAID · BROAD INSTITUTE, INC. · PI NEAFSEY, DANIEL E · 2014 to 2024
$66.5M
Epidemiologic and molecular basis of the gut-urinary tract axis in urinary tract infectionR01DK121822 · NIDDK · WASHINGTON UNIVERSITY · PI Ashlee Miriam Earl, SCOTT J. HULTGREN · 2020 to 2026
$4.9M
Machine Learning and Control Principles for Computational BiologyR35GM143056 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI GIBSON, TRAVIS ELI · 2021 to 2025
$2.2M
Manifold representations and active learning for 21 st century biologyR35GM141861 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BERGER, BONNIE · 2021 to 2025
$1.9M
Probabilistic deep learning models and integrated biological experiments for analyzing dynamic and heterogeneous microbiomesR35GM149270 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Georg Kurt Gerber · 2023 to 2026
$1.8M
Bayesian Machine Learning Tools for Analyzing Microbiome DynamicsR01GM130777 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI GERBER, GEORG KURT · 2018 to 2022
$1.6M
Tracking the microbiome: purpose-built machine learning tools for tracking microbial strains over timeR21AI154075 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI GIBSON, TRAVIS ELI · 2021 to 2022
$492k
NIAID NIH HHS R21 AI154075NIAID NIH HHS U19 AI110818NIDDK NIH HHS R01 DK121822NIGMS NIH HHS R01 GM130777NIGMS NIH HHS R35 GM141861NIGMS NIH HHS R35 GM143056NIGMS NIH HHS R35 GM149270U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DK121822U.S. Department of Health & Human Services | National Institutes of Health (NIH) R21AI154075U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM141861U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM143056U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM149270U.S. Department of Health & Human Services | National Institutes of Health (NIH) U19AI110818
6 · The paper itself

Abstract

The ability to detect and quantify microbiota over time from shotgun metagenomic data has a plethora of clinical, basic science and public health applications. Given these applications, and the observation that pathogens and other taxa of interest can reside at low relative abundance, there is a critical need for algorithms that accurately profile low-abundance microbial taxa with strain-level resolution. Here we present ChronoStrain: a sequence quality- and time-aware Bayesian model for profiling strains in longitudinal samples. ChronoStrain explicitly models the presence or absence of each strain and produces a probability distribution over abundance trajectories for each strain. Using synthetic and semi-synthetic data, we demonstrate how ChronoStrain outperforms existing methods in abundance estimation and presence/absence prediction. Applying ChronoStrain to two human microbiome datasets demonstrated its improved interpretability for profiling Escherichia coli strain blooms in longitudinal faecal samples from adult women with recurring urinary tract infections, and its improved accuracy for detecting Enterococcus faecalis strains in infant faecal samples. Compared with state-of-the-art methods, ChronoStrain's ability to detect low-abundance taxa is particularly stark.

Indexed as

BacteriaMetagenomicsMicrobiotaAdultAlgorithmsBayes TheoremEnterococcus faecalisEscherichia coliFecesFemaleHumansInfantLongitudinal Studies

Identifiers

PMID40328944
PMCPMC12122369

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.