Evidence map›Paper›PMID 41477820›Full record

ArticleScience advances2026

Machine learning-powered single-molecule cancer diagnosis using DNA origami tags.

Jinxin Xiong, Zhimei He, Wenyan Guan, Sheng Zhi, Xing Sun, Zixiao Yang, Jianfeng Ma, Chunhai Fan, Lianhui Wang, Jie Chao

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jinxin XiongState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.ORCID 0009-0006-8723-9154
Zhimei HeState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.ORCID 0000-0002-8509-0142
Wenyan GuanDepartment of Pathology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China.ORCID 0000-0003-3129-9730
Sheng ZhiState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Xing SunState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Zixiao YangState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Jianfeng MaState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Chunhai FanState Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhang Jiang Institute for Advanced Study and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, China.ORCID 0000-0002-7171-7338
Lianhui WangState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.ORCID 0000-0001-9030-9172
Jie ChaoState Key Laboratory for Flexible Electronics (LoFE), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.ORCID 0000-0003-1030-9944

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-molecule detection (SMD) holds considerable promise in biomedical research. Although atomic force microscopy (AFM) provides an important technique with nanoscale resolution for SMD, its broader application is limited by labeling challenges and slow data processing. Here, we present a machine learning (ML)-powered strategy combining AFM and DNA nanotags for SMD and cancer diagnosis. Nickases are applied to create specific single-strand breaks in target DNA, allowing insertion of exogenous DNA to attach shape-distinct nanotags for AFM imaging. A YOLOv5l algorithm is adopted to automatically recognize target objects in AFM images, which can classify 370 structures in 1.21 seconds with 98% accuracy. The proof of concept of this strategy is confirmed by identifying nickase-edited sites on both linear and circular DNA. Its practical applicability is demonstrated by detecting KRAS Gly12Arg (G12R) and p53 Arg175His (R175H) mutations in samples from patients with pancreatic and colorectal cancer, with accuracy rivaling Sanger sequencing and quantitative polymerase chain reaction, opening avenues for SMD.

Indexed as

DNAMachine LearningNeoplasmsPancreatic NeoplasmsSingle Molecule ImagingAlgorithmsColorectal NeoplasmsHumansMicroscopy, Atomic ForceMutationProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53DNAKRAS protein, humanProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53

Identifiers

PMID41477820
PMCPMC12757023

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.