Evidence map›Paper›PMID 37306408›Full record

ArticleGut microbes

MMINP: A computational framework of microbe-metabolite interactions-based metabolic profiles predictor based on the O2-PLS algorithm.

Wenli Tang, Huimin Zheng, Shuangbin Xu, Pan Li, Li Zhan, Xiao Luo, Zehan Dai, Qianwen Wang, Guangchuang Yu

Open access · goldAbstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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, 8 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

Wenli TangDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Huimin ZhengDepartment of Obstetrics and Gynecology, First People's Hospital of Foshan, Foshan, Guangdong, China.
Shuangbin XuDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Pan LiMicrobiome Research Centre, St. George and Sutherland Clinical School, Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.
Li ZhanDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Xiao LuoDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Zehan DaiDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Qianwen WangDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Guangchuang YuDepartment of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID 0000-0002-6485-8781
Southern Medical University · CNFirst People's Hospital of Foshan · CNSutherland Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut metabolome acts as an intermediary between the gut microbiota and host, and has tremendous diagnostic and therapeutic potential. Several studies have utilized bioinformatic tools to predict metabolites based on the different aspects of the gut microbiome. Although these tools have contributed to a better understanding of the relationship between the gut microbiota and various diseases, most of them have focused on the impact of microbial genes on the metabolites and the relationship between microbial genes. In contrast, relatively little is known regarding the effect of metabolites on the microbial genes or the relationship between these metabolites. In this study, we constructed a computational framework of Microbe-Metabolite INteractions-based metabolic profiles Predictor (MMINP), based on the Two-Way Orthogonal Partial Least Squares (O2-PLS) algorithm to predict the metabolic profiles associated with gut microbiota. We demonstrated the predictive value of MMINP relative to that of similar methods. Additionally, we identified the features that would profoundly impact the prediction performance of data-driven methods (O2-PLS, MMINP, MelonnPan, and ENVIM), including the training sample size, host disease state, and the upstream data processing methods of the different technical platforms. We suggest that when using data-driven methods, similar host disease states and preprocessing methods, and a sufficient number of training samples are necessary to achieve accurate prediction.

Indexed as

Gastrointestinal MicrobiomeAlgorithmsComputational BiologyLeast-Squares AnalysisMetabolomedata-driven methodmetabolomemetagenomeprediction

Identifiers

PMID37306408
PMCPMC10262779
OpenAlexW4380291875

What OpenQuestion holds

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LicenceCC BY-NC
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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.