Evidence map›Paper›PMID 42245499›Full record

ArticleFrontiers in microbiology2026

A transformer based deep learning framework for accurate single nucleotide variant correction in heterogeneous samples.

Xiaonan Wang, Shenjie Wang, Zhili Chang, Minchao Zhao, Xian Zhang, Nazarov Fayzullo, Eshtemirov Bunyod, Shuotong Li, Jiayin Wang

Abstract read
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Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Xiaonan WangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Shenjie WangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Zhili ChangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Minchao ZhaoSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Xian ZhangNanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.
Nazarov FayzulloAI and Digital Technologies Faculty, Samarkand State University, Samarkand, Uzbekistan.
Eshtemirov BunyodAI and Digital Technologies Faculty, Samarkand State University, Samarkand, Uzbekistan.
Shuotong LiCollege of Economics, Shenzhen University, Shenzhen, China.
Jiayin WangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Profiling host genetic variations in heterogeneous host-microbiome mixtures is crucial for understanding cross-species interactions and microenvironmental dynamics. However, the variable host DNA fraction (purity) in bulk sequencing data severely compromises the performance of standard variant callers, leading to significant systematic biases in quantifying single nucleotide variants (SNVs). To address this, we developed a Transformer-based computational framework designed to model sequence context and technical artifacts in low-purity samples. The architecture employs a group-encoding mechanism to process multidimensional features-including variant allele frequency (VAF) distributions, base-level purity estimates, sequencing depth, and local genomic context (such as repeat regions and chromatin accessibility). By capturing long-range dependencies among these diverse signals, the model effectively neutralizes purity-induced biases to accurately recover the true host SNV count. We evaluated the framework using simulated sequencing data across a broad purity gradient (0.2-1.0). Our approach significantly reduced quantification errors, achieving high concordance between the corrected and actual ground-truth SNV counts. Benchmarking the corrected counts against the raw outputs of conventional callers (Mutect, Freebayes, LoFreq, and Platypus) demonstrated substantial performance gains, particularly in ultra-low purity conditions (0.2-0.3) where traditional statistical priors typically fail to provide reliable quantifications. Feature ablation and residual analyses further validated the independence of the multidimensional inputs and the unbiased, zero-centered nature of the count corrections. This deep learning pipeline provides a robust solution for the accurate quantification of host SNVs in complex biological mixtures, facilitating reliable downstream genetic analyses in highly heterogeneous microenvironments.

Indexed as

genomic profilingheterogeneous sampleshost-microbe symbiosissingle nucleotide variant correctiontransformer architecture

Identifiers

PMID42245499
PMCPMC13230899

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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.