Evidence map›Paper›PMID 39735577›Full record

ArticleBioinformatics advances2025

Multitask knowledge-primed neural network for predicting missing metadata and host phenotype based on human microbiome.

Mahsa Monshizadeh, Yuhui Hong, Yuzhen Ye

Abstract read
In one paragraph

Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

3 authors.

Mahsa MonshizadehComputer Science Department, Indiana University, Bloomington, IN 47408, United States.
Yuhui HongComputer Science Department, Indiana University, Bloomington, IN 47408, United States.ORCID https://orcid.org/0000-0002-5647-9714
Yuzhen YeComputer Science Department, Indiana University, Bloomington, IN 47408, United States.ORCID https://orcid.org/0000-0003-3707-3185

Funding

Subtractive assembly approaches for inferring disease-associated microbial genes and pathways from microbiome sequencing dataR01AI143254 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI YE, YUZHEN · 2019 to 2023
$1.1M
NIAID NIH HHS R01 AI143254
6 · The paper itself

Abstract

Motivation: Microbial signatures in the human microbiome are closely associated with various human diseases, driving the development of machine learning models for microbiome-based disease prediction. Despite progress, challenges remain in enhancing prediction accuracy, generalizability, and interpretability. Confounding factors, such as host's gender, age, and body mass index, significantly influence the human microbiome, complicating microbiome-based predictions. Results: To address these challenges, we developed MicroKPNN-MT, a unified model for predicting human phenotype based on microbiome data, as well as additional metadata like age and gender. This model builds on our earlier MicroKPNN framework, which incorporates prior knowledge of microbial species into neural networks to enhance prediction accuracy and interpretability. In MicroKPNN-MT, metadata, when available, serves as additional input features for prediction. Otherwise, the model predicts metadata from microbiome data using additional decoders. We applied MicroKPNN-MT to microbiome data collected in mBodyMap, covering healthy individuals and 25 different diseases, and demonstrated its potential as a predictive tool for multiple diseases, which at the same time provided predictions for the missing metadata. Our results showed that incorporating real or predicted metadata helped improve the accuracy of disease predictions, and more importantly, helped improve the generalizability of the predictive models. Availability and implementation: https://github.com/mgtools/MicroKPNN-MT.

Identifiers

PMID39735577
PMCPMC11676323

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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.