ArticleBioinformatics (Oxford, England)2018
MicroPheno: predicting environments and host phenotypes from 16S rRNA gene sequencing using a k-mer based representation of shallow sub-samples.
Article in Bioinformatics (Oxford, England), 2018. 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 39 papers.
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Who cites it
39 citing papers in PubMed.
- Review
- Smart Microbiomes: How AI Is Revolutionizing Personalized Medicine.Bioengineering (Basel, Switzerland) · 2025Review
- Integrating sequence composition information into microbial diversity analyses with k-mer frequency counting.mSystems · 2025Article
- EPheClass: ensemble-based phenotype classifier from 16S rRNA gene sequences.Frontiers in bioinformatics · 2025Article
- Benchmarking beta-diversity measures and transfer functions for sedimentary ancient DNA.ISME communications · 2025Article
- A deep learning feature importance test framework for integrating informative high-dimensional biomarkers to improve disease outcome prediction.Briefings in bioinformatics · 2024Article
- Utilizing Artificial Intelligence for Microbiome Decision-Making: Autism Spectrum Disorder in Children from Bosnia and Herzegovina.Diagnostics (Basel, Switzerland) · 2024Article
- Metabolic interactions shape emergent biofilm structures in a conceptual model of gut mucosal bacterial communities.NPJ biofilms and microbiomes · 2024Article
- Deep learning methods in metagenomics: a review.Microbial genomics · 2024Review
- Deep learning in microbiome analysis: a comprehensive review of neural network models.Frontiers in microbiology · 2024Review
- Reorganizing heterogeneous information from host-microbe interaction reveals innate associations among samples.Quantitative biology (Beijing, China) · 2023Article
- Crohn's Disease Prediction Using Sequence Based Machine Learning Analysis of Human Microbiome.Diagnostics (Basel, Switzerland) · 2023Article
- Automatic disease prediction from human gut metagenomic data using boosting GraphSAGE.BMC bioinformatics · 2023Article
- MV-CVIB:Frontiers in microbiology · 2023Article
- NN-RNALoc: Neural network-based model for prediction of mRNA sub-cellular localization using distance-based sub-sequence profiles.PloS one · 2023Article
- A convenient correspondence between k-mer-based metagenomic distances and phylogenetically-informed β-diversity measures.PLoS computational biology · 2023Article
- Microbiome-based disease prediction with multimodal variational information bottlenecks.PLoS computational biology · 2022Article
- Article
- Multimodal deep learning applied to classify healthy and disease states of human microbiome.Scientific reports · 2022Article
- Metagenomic Predictions: A Review 10 years on.Frontiers in genetics · 2022Review
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Motivation: Microbial communities play important roles in the function and maintenance of various biosystems, ranging from the human body to the environment. A major challenge in microbiome research is the classification of microbial communities of different environments or host phenotypes. The most common and cost-effective approach for such studies to date is 16S rRNA gene sequencing. Recent falls in sequencing costs have increased the demand for simple, efficient and accurate methods for rapid detection or diagnosis with proved applications in medicine, agriculture and forensic science. We describe a reference- and alignment-free approach for predicting environments and host phenotypes from 16S rRNA gene sequencing based on k-mer representations that benefits from a bootstrapping framework for investigating the sufficiency of shallow sub-samples. Deep learning methods as well as classical approaches were explored for predicting environments and host phenotypes. Results: A k-mer distribution of shallow sub-samples outperformed Operational Taxonomic Unit (OTU) features in the tasks of body-site identification and Crohn's disease prediction. Aside from being more accurate, using k-mer features in shallow sub-samples allows (i) skipping computationally costly sequence alignments required in OTU-picking and (ii) provided a proof of concept for the sufficiency of shallow and short-length 16S rRNA sequencing for phenotype prediction. In addition, k-mer features predicted representative 16S rRNA gene sequences of 18 ecological environments, and 5 organismal environments with high macro-F1 scores of 0.88 and 0.87. For large datasets, deep learning outperformed classical methods such as Random Forest and Support Vector Machine. Availability and implementation: The software and datasets are available at https://llp.berkeley.edu/micropheno. Supplementary information: Supplementary data are available at Bioinformatics online.
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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.