Evidence map›Paper›PMID 40919911›Full record

ArticleBriefings in bioinformatics2025

TMBquant: an explainable AI-powered caller advancing tumor mutation burden quantification across heterogeneous samples.

Shenjie Wang, Xiaonan Wang, Xiaoyan Zhu, Xuwen Wang, Yuqian Liu, Minchao Zhao, Zhili Chang, Yang Shao, Haitao Zhang, Shuanying Yang and 1 more

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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

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.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

11 authors.

Shenjie WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710004, China.
Xiaonan WangSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Xiaoyan ZhuSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Xuwen WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710004, China.
Yuqian LiuSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Minchao ZhaoNanjing Geneseeq Technology Inc., 128 Huakang Road, Pukou, Nanjing 211800, China.
Zhili ChangNanjing Geneseeq Technology Inc., 128 Huakang Road, Pukou, Nanjing 211800, China.
Yang ShaoNanjing Geneseeq Technology Inc., 128 Huakang Road, Pukou, Nanjing 211800, China.ORCID 0000-0003-4585-1792
Haitao ZhangDepartment of Respiratory Medicine, Tangdu Hospital, The Fourth Military Medical University, 569 Xinsi Road, Baqiao District, Xi'an, Shaanxi 710038, China.
Shuanying YangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710004, China.
Jiayin WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710004, China.ORCID 0000-0002-3862-6557

Funding

National Natural Science Foundation of China 62402376National Natural Science Foundation of China 72274152National Natural Science Foundation of China 72293581Natural Science Basic Research Program of Shaanxi 2020JC-01
6 · The paper itself

Abstract

Accurate tumor mutation burden (TMB) quantification is critical for immunotherapy stratification, yet remains challenging due to variability across sequencing platforms, tumor heterogeneity, and variant calling pipelines. Here, we introduce TMBquant, an explainable AI-powered caller designed to optimize TMB estimation through dynamic feature selection, ensemble learning, and automated strategy adaptation. Built upon the H2O AutoML framework, TMBquant integrates variant features, minimizes classification errors, and enhances both accuracy and stability across diverse datasets. We benchmarked TMBquant against nine widely used variant callers, including traditional tools (e.g. Mutect2, VarScan2, Strelka2) and recent AI-based methods (DeepSomatic, Octopus), using 706 whole-exome sequencing tumor-control pairs. To evaluate clinical relevance, we further assessed TMBquant through survival analyses across immunotherapy-treated cohorts of non-small cell lung cancer (NSCLC), nasopharyngeal carcinoma (NPC), and the two NSCLC subtypes: lung adenocarcinoma and lung squamous cell carcinoma. In each cohort, TMBquant consistently achieved the highest hazard ratios, demonstrating superior patient stratification compared to all other methods. Importantly, TMBquant maintained robust predictive performance across both high-TMB (NSCLC) and low-TMB (NPC) settings, highlighting its generalizability across cancer types with distinct biological characteristics. These findings establish TMBquant as a reliable, reproducible, and clinically actionable tool for precision oncology. The software is open source and freely available at https://github.com/SomaticCaller/SomaticCaller. To enhance reproducibility, we provide detailed usage instructions and representative code snippets for TMBquant in the Methods section (see Code Availability).

Indexed as

Artificial IntelligenceBiomarkers, TumorCarcinoma, Non-Small-Cell LungLung NeoplasmsMutationNeoplasmsSoftwareComputational BiologyExome SequencingHumansBiomarkers, Tumorcounting-based biomarkerheterogeneous samplesimmunotherapytumor mutation burdenvariant calling

Identifiers

PMID40919911
PMCPMC12415849

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.