BMC GenomicsGenetic & Genomic MedicinePeer-reviewed journal article
Frequentmers - a novel way to look at metagenomic Next Generation Sequencing data and an application in detecting liver cirrhosis
Ioannis MouratidisiD, Nikol ChantziiD, Umair KhaniD, Maxwell A. KonnarisiD, Candace S. Y. ChaniD, Manvita MareboinaiD, Camille M. MoeckeliD, Ilias Georgakopoulos‐SoaresiD
Abstract
Early detection of human disease is associated with improved clinical outcomes. However, many diseases are often detected at an advanced, symptomatic stage where patients are past efficacious treatment periods and can result in less favorable outcomes. Therefore, methods that can accurately detect human disease at a presymptomatic stage are urgently needed. Here, we introduce "frequentmers"; short sequences that are specific and recurrently observed in either patient or healthy control samples, but not in both. We showcase the utility of frequentmers for the detection of liver cirrhosis using metagenomic Next Generation Sequencing data from stool samples of patients and controls. We develop classification models for the detection of liver cirrhosis and achieve an AUC score of 0.91 using ten-fold cross-validation. A small subset of 200 frequentmers can achieve comparable results in detecting liver cirrhosis. Finally, we identify the microbial organisms in liver cirrhosis samples, which are associated with the most predictive frequentmer biomarkers.
- organism: human
- assay: metagenomics
- research focus: differential expression
- approach: statistical model
- Citations
- 3
- FWCI
- 0.27
- Field percentile
- 45th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Early prediction of liver disease using conventional risk factors and gut microbiome-augmented gradient boosting
Yang Liu, Guillaume Méric, … Michael Inouye·Cell MetabolismPeer-reviewed·Mar 29, 2022
- MetagenBERT: a Transformer Architecture using Foundational DNA Read Embedding Models to enhance Disease Classification
Gaspar Roy, Eugeni Belda, … Jean‐Daniel Zucker·bioRxiv·May 6, 2025
- A robust, sensitive phylogenetic method enables gene-level metagenomic analyses
Nghi Tran, Kathryn Kananen, Patrick H. Bradley·bioRxiv·Jul 15, 2026
- Metagenomic unmapped reads provide important insights into human microbiota and disease associations
Zifan Zhu, Jie Ren, … Fengzhu Sun·Genome biologyPeer-reviewed·Aug 6, 2019
- Microbiome meta-analysis and cross-disease comparison enabled by the SIAMCAT machine-learning toolbox
Jakob Wirbel, Konrad Zych, … Georg Zeller·Genome biologyPeer-reviewed·Mar 30, 2021
- A novel algorithm to accurately classify metagenomic sequences
Subrata Saha, Zigeng Wang, Sanguthevar Rajasekaran·bioRxiv·Oct 1, 2020