Evidence map›Paper›PMID 41499226›Full record

ArticleBioinformatics (Oxford, England)2026

NanoSSL: attention mechanism-based self-supervised learning method for protein identification using nanopores.

Yong Xie, Jindong Li, Ziyan Zhang, Bin Meng, Shuaijian Dai, Yuchen Zhou, Eamonn Kennedy, Niandong Jiao, Haobin Chen, Zhuxin Dong

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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.

Yong XieDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Jindong LiDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Ziyan ZhangDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Bin MengDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Shuaijian DaiDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Yuchen ZhouXiangya School of Medicine, Central South University, Changsha, Hunan 410013, China.
Eamonn KennedyDivision of Epidemiology, Internal Medicine, University of Utah, Salt Lake City, UT 84112, United States.
Niandong JiaoState Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang, Liaoning 110169, China.
Haobin ChenDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.
Zhuxin DongDepartment of Biomedical Engineering, Xiangya School of Basic Medical Sciences, Central South University, Changsha, Hunan 410013, China.ORCID 0000-0001-9059-2430

Funding

National Key R&D Program of China 2023YFF1205900National Natural Science Foundation of China 32271520State Key Laboratory of Robotics 2023005
6 · The paper itself

Abstract

motivationNanopores are cutting-edge interdisciplinary tools that can analyze biomolecules at the single-molecule level for many applications, e.g. DNA sequencing. Efforts are underway to extend nanopores to proteomics, including the development of machine learning algorithms for protein sequencing and identification. However, single-molecule data are intrinsically noisy and hard to process. Moreover, the development and performance of machine learning for nanopore is jeopardized by data scarcity. Self-supervised learning is an emerging method that may yield advantages in nanopore scenarios.

resultsWe propose and experimentally validate Nanopore analysis using Self-Supervised Learning (NanoSSL), a generative self-supervised learning framework based on attention mechanisms for the identification of protein signals from nanopores. Leveraging a two-step approach consisting of self-supervised pre-training and supervised fine-tuning, NanoSSL learns useful feature representations from empirical data to facilitate downstream classification tasks. Inspired by the concept of fragmentation in conventional protein sequencing technologies, during pretraining each translocation event is split into multiple non-overlapping fragments of equal size, some of which are randomly masked and reconstructed using a masked autoencoder. Learning the feature representations of the reconstructed nanopore events facilitates molecular identification in fine-tuning. In this study, we retested a publicly available nanopore multiplexed protein sensing dataset for model iteration, and subsequently measured Alzheimer's disease biomarker Aβ1-42 using homemade solid-state nanopores. Empirical results indicated NanoSSL achieved an unprecedented performance across four metrics: accuracy, precision, recall, and F1 score, when classifying two mutated Aβ1-42, E22G and G37R. The self-supervised learning and attention mechanism were verified as the source of performance gains. AVAILABILITY AND IMPLEMENTATION: The main program is available at https://doi.org/10.5281/zenodo.17172822.

Indexed as

NanoporesProteinsProteomicsSupervised Machine LearningAlgorithmsAmyloid beta-PeptidesHumansAmyloid beta-PeptidesProteins

Identifiers

PMID41499226
PMCPMC12777981

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.