Evidence map›Paper›PMID 41092060›Full record

ArticleBriefings in bioinformatics2025

MRDadaptis: self-adaptive parameter configuration enhances minimal residual disease detection in heterogeneous ctDNA samples.

Tianci Wang, Xin Lai, Shenjie Wang, Zhengfa Xue, Yuqian Liu, Xiaoyan Zhu, Xiaonan Wang, Zhili Chang, Yang Shao, Xian Zhang 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.

Tianci WangSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.ORCID 0000-0002-4875-3488
Xin LaiSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Shenjie WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University,  No. 157, Xiwu Road, Xincheng District, Xi'an 710003, China.
Zhengfa XueSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Yuqian LiuSchool 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.
Xiaonan WangNanjing 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
Xian ZhangNanjing Geneseeq Technology Inc., 128 Huakang Road, Pukou, Nanjing 211800, China.
Jiayin WangSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.ORCID 0000-0002-3862-6557

Funding

National Natural Science Foundation of China 62402376National Natural Science Foundation of China 62572389National Natural Science Foundation of China 72274152National Natural Science Foundation of China 72293581
6 · The paper itself

Abstract

Detection of structural variations (SVs) through circulating tumor DNA (ctDNA) has become a key method for detecting minimal residual disease (MRD). However, the heterogeneity of ctDNA samples, characterized by variable limits of detection (LOD) and diverse structural variant types, significantly impacts detection stability and performance, posing persistent challenges for conventional SV detection tools such as Delly and Manta. These widely used methods require extensive manual parameter tuning, hindered by the combinatorial complexity of multiple parameters and heterogeneous sequencing data. To address this, we propose MRDadaptis, a novel SV detection tool that uniquely incorporates a self-adaptive parameter optimization mechanism. MRDadaptis distinguishes itself by integrating Bayesian optimization with meta-learning techniques to dynamically adjust detection parameters automatically, based on intrinsic features derived from the ctDNA sequencing data itself. This innovative approach not only reduces manual intervention but also effectively captures sample-specific characteristics, significantly improving detection stability, and detection performance. Extensive validation experiments using both simulated and real-world ctDNA datasets demonstrates it distinct advantages, including markedly improved average F1-scores and superior stability (reduced variance, lower RMSE, increased kurtosis). These results highlight the significant advantages of MRDadaptis in addressing sample heterogeneity, underscoring its potential to improve the accuracy and reliability of MRD detecting through ctDNA analysis. https://github.com/aAT0047/MRDadaptis.git.

Indexed as

Circulating Tumor DNANeoplasm, ResidualSoftwareAlgorithmsBayes TheoremHumansCirculating Tumor DNABayesian optimizationctDNAheterogeneous sequencing samplemeta-learningself-adaptive parameter configurationstructural variant detection

Identifiers

PMID41092060
PMCPMC12527258

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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.