Evidence map›Paper›PMID 40178927›Full record

ArticleBioinformatics (Oxford, England)2025

Demixer: a probabilistic generative model to delineate different strains of a microbial species in a mixed infection sample.

Brintha Vp, Manikandan Narayanan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Brintha VpDepartment of Computer Science and Engineering, Indian Institute of Technology (IIT) Madras, Chennai, 600036, India.ORCID 0009-0002-2300-8171
Manikandan NarayananDepartment of Computer Science and Engineering, Indian Institute of Technology (IIT) Madras, Chennai, 600036, India.ORCID 0000-0002-8490-4087

Funding

Wellcome TrustWellcome Trust/DBT IA/I/17/2/503323
6 · The paper itself

Abstract

motivationMulti-drug resistant or hetero-resistant tuberculosis (TB) hinders the successful treatment of TB. Hetero-resistant TB occurs when multiple strains of the TB-causing bacterium with varying degrees of drug susceptibility are present in an individual. Existing studies predicting the proportion and identity of strains in a mixed infection sample rely on a reference database of known strains. A main challenge then is to identify de novo strains not present in the reference database, while quantifying the proportion of known strains.

resultsWe present Demixer, a probabilistic generative model that uses a combination of reference-based and reference-free techniques to delineate mixed infection strains in whole genome sequencing (WGS) data. Demixer extends a topic model widely used in text mining to represent known mutations and discover novel ones. Parallelization and other heuristics enabled Demixer to process large datasets like CRyPTIC (Comprehensive Resistance Prediction for Tuberculosis: an International Consortium). In both synthetic and experimental benchmark datasets, our proposed method precisely detected the identity (e.g. 91.67% accuracy on the experimental in vitro dataset) as well as the proportions of the mixed strains. In real-world applications, Demixer revealed novel high confidence mixed infections (101 out of 1963 Malawi samples analysed), and new insights into the global frequency of mixed infection (2% at the most stringent threshold in the CRyPTIC dataset) and its significant association to drug resistance. Our approach is generalizable and hence applicable to any bacterial and viral WGS data. AVAILABILITY AND IMPLEMENTATION: All code relevant to Demixer is available at https://github.com/BIRDSgroup/Demixer.

Indexed as

CoinfectionModels, StatisticalMycobacterium tuberculosisSoftwareTuberculosis, Multidrug-ResistantComputational BiologyGenome, BacterialHumansWhole Genome SequencingCRyPTIC consortiumhybrid (reference-plus-de novo) approachLatent Dirichilet Allocation (LDA)latent variable modelingmixed infectionmulti-sample analysismutationsparallel heuristicsstrainsTuberculosis (TB)Whole Genome Sequencing (WGS)

Identifiers

PMID40178927
PMCPMC12011361

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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.