Evidence map›Paper›PMID 39311770›Full record

ArticleMicrobiology spectrum2024

An integrated strain-level analytic pipeline utilizing longitudinal metagenomic data.

Boyan Zhou, Chan Wang, Gregory Putzel, Jiyuan Hu, Menghan Liu, Fen Wu, Yu Chen, Alejandro Pironti, Huilin Li

Abstract read
In one paragraph

Article in Microbiology spectrum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
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

9 authors.

Boyan ZhouDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, New York, USA.ORCID 0000-0001-7067-4578
Chan WangDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, New York, USA.
Gregory PutzelDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Jiyuan HuDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, New York, USA.
Menghan LiuDepartment of Biological Sciences, Columbia University in the City of New York, New York, New York, USA.
Fen WuDivision of Epidemiology, Department of Population Health, New York University School of Medicine, New York, New York, USA.
Yu ChenDivision of Epidemiology, Department of Population Health, New York University School of Medicine, New York, New York, USA.
Alejandro PirontiDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Huilin LiDivision of Biostatistics, Department of Population Health, New York University School of Medicine, New York, New York, USA.ORCID 0000-0002-8288-7068

Funding

Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer RiskR01CA204113 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHEN, YU, PEI, ZHIHENG · 2016 to 2020
$3.8M
The Oral Microbiome and Upper Aerodigestive Squamous Cell CancerR01CA159036 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG, HAYES, RICHARD BERNARD · 2011 to 2024
$3.5M
Project 2P20CA252728 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG · 2020 to 2022
$3.4M
Prospective Study of Human Oral Microbiome and Pancreatic Cancer RiskR01CA164964 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG · 2014 to 2017
$2.2M
Novel Computational Methods for Microbiome Data Analysis in Longitudinal StudyR01LM014085 · NLM · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Huilin Li · 2023 to 2026
$1.5M
HHS | National Institutes of Health (NIH) P20CA252728,R01LM014085HHS | National Institutes of Health (NIH) R01CA204113NCI NIH HHS P20 CA252728NCI NIH HHS R01 CA164964NCI NIH HHS R01 CA204113NLM NIH HHS R01 LM014085
6 · The paper itself

Abstract

With the development of sequencing technology and analytic tools, studying within-species variations enhances the understanding of microbial biological processes. Nevertheless, most existing methods designed for strain-level analysis lack the capability to concurrently assess both strain proportions and genome-wide single nucleotide variants (SNVs) across longitudinal metagenomic samples. In this study, we introduce LongStrain, an integrated pipeline for the analysis of large-scale metagenomic data from individuals with longitudinal or repeated samples. In LongStrain, we first utilize two efficient tools, Kraken2 and Bowtie2, for the taxonomic classification and alignment of sequencing reads, respectively. Subsequently, we propose to jointly model strain proportions and shared haplotypes across samples within individuals. This approach specifically targets tracking a primary strain and a secondary strain for each subject, providing their respective proportions and SNVs as output. With extensive simulation studies of a microbial community and single species, our results demonstrate that LongStrain is superior to two genotyping methods and two deconvolution methods across a majority of scenarios. Furthermore, we illustrate the potential applications of LongStrain in the real data analysis of The Environmental Determinants of Diabetes in the Young study and a gastric intestinal metaplasia microbiome study. In summary, the proposed analytic pipeline demonstrates marked statistical efficiency over the same type of methods and has great potential in understanding the genomic variants and dynamic changes at strain level. LongStrain and its tutorial are freely available online at https://github.com/BoyanZhou/LongStrain. IMPORTANCE: The advancement in DNA-sequencing technology has enabled the high-resolution identification of microorganisms in microbial communities. Since different microbial strains within species may contain extreme phenotypic variability (e.g., nutrition metabolism, antibiotic resistance, and pathogen virulence), investigating within-species variations holds great scientific promise in understanding the underlying mechanism of microbial biological processes. To fully utilize the shared genomic variants across longitudinal metagenomics samples collected in microbiome studies, we develop an integrated analytic pipeline (LongStrain) for longitudinal metagenomics data. It concurrently leverages the information on proportions of mapped reads for individual strains and genome-wide SNVs to enhance the efficiency and accuracy of strain identification. Our method helps to understand strains' dynamic changes and their association with genome-wide variants. Given the fast-growing longitudinal studies of microbial communities, LongStrain which streamlines analyses of large-scale raw sequencing data should be of great value in microbiome research communities.

Indexed as

MetagenomicsBacteriaComputational BiologyGastrointestinal MicrobiomeHigh-Throughput Nucleotide SequencingHumansLongitudinal StudiesMetagenomeMicrobiotaPolymorphism, Single NucleotideSequence Analysis, DNASoftwaregenomic variantslongitudinal metagenomic datamicrobiomestrain dynamicsstrain-level analysis

Identifiers

PMID39311770
PMCPMC11542597

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LicenceCC BY
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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.