Evidence map›Paper›PMID 30367598›Full record

ArticleBMC bioinformatics2018

BMCMDA: a novel model for predicting human microbe-disease associations via binary matrix completion.

Jian-Yu Shi, Hua Huang, Yan-Ning Zhang, Jiang-Bo Cao, Siu-Ming Yiu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  15. Application of Machine Learning in Microbiology.Frontiers in microbiology · 2019
    Review
  16. 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

5 authors.

Jian-Yu ShiSchool of Life Sciences, Northwestern Polytechnical University, Xi'an, 70072, China. jianyushi@nwpu.edu.cn.
Hua HuangSchool of Software and Microelectronics, Northwestern Polytechnical University, Xi'an, 70072, China.
Yan-Ning ZhangSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 70072, China.
Jiang-Bo CaoSchool of Life Sciences, Northwestern Polytechnical University, Xi'an, 70072, China.
Siu-Ming YiuDepartment of Computer Science, The University of Hong Kong, Hong Kong, 999077, China.

Funding

Urokinase-type Plasminogen Activator System and Pancreatic Stellate CellsR03AA016008 · NIAAA · BRENTWOOD BIOMEDICAL RESEARCH INSTITUTE · PI LUGEA, AURELIA · 2006 to 2007
$122k
NIAAA NIH HHS R03 AA016008
6 · The paper itself

Abstract

backgroundHuman Microbiome Project reveals the significant mutualistic influence between human body and microbes living in it. Such an influence lead to an interesting phenomenon that many noninfectious diseases are closely associated with diverse microbes. However, the identification of microbe-noninfectious disease associations (MDAs) is still a challenging task, because of both the high cost and the limitation of microbe cultivation. Thus, there is a need to develop fast approaches to screen potential MDAs. The growing number of validated MDAs enables us to meet the demand in a new insight. Computational approaches, especially machine learning, are promising to predict MDA candidates rapidly among a large number of microbe-disease pairs with the advantage of no limitation on microbe cultivation. Nevertheless, a few computational efforts at predicting MDAs are made so far.

resultsIn this paper, grouping a set of MDAs into a binary MDA matrix, we propose a novel predictive approach (BMCMDA) based on Binary Matrix Completion to predict potential MDAs. The proposed BMCMDA assumes that the incomplete observed MDA matrix is the summation of a latent parameterizing matrix and a noising matrix. It also assumes that the independently occurring subscripts of observed entries in the MDA matrix follows a binomial model. Adopting a standard mean-zero Gaussian distribution for the nosing matrix, we model the relationship between the parameterizing matrix and the MDA matrix under the observed microbe-disease pairs as a probit regression. With the recovered parameterizing matrix, BMCMDA deduces how likely a microbe would be associated with a particular disease. In the experiment under leave-one-out cross-validation, it exhibits the inspiring performance (AUC = 0.906, AUPR =0.526) and demonstrates its superiority by ~ 7% and ~ 5% improvements in terms of AUC and AUPR respectively in the comparison with the pioneering approach KATZHMDA.

conclusionsOur BMCMDA provides an effective approach for predicting MDAs and can be also extended to other similar predicting tasks of binary relationship (e.g. protein-protein interaction, drug-target interaction).

Indexed as

AlgorithmsBacteriaDiseaseMicrobiotaModels, BiologicalBacterial Physiological PhenomenaComputational BiologyHost-Pathogen InteractionsHumansRisk FactorsMachine learningMatrix completionMicrobe-disease associationPrediction

Identifiers

PMID30367598
PMCPMC6101089

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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.