Evidence map›Paper›PMID 39402441›Full record

ArticleBMC bioinformatics2024

DNASimCLR: a contrastive learning-based deep learning approach for gene sequence data classification.

Minghao Yang, Zehua Wang, Zizhuo Yan, Wenxiang Wang, Qian Zhu, Changlong Jin

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. CLASPP: A unified model for predicting post-translational modifications.bioRxiv : the preprint server for biology · 2026
    Article
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Minghao YangShandong University, Weihai, People's Republic of China.
Zehua WangBeijing Research Institute of Automation for Machinery Industry, Beijing, People's Republic of China.
Zizhuo YanBeijing Research Institute of Automation for Machinery Industry, Beijing, People's Republic of China.
Wenxiang WangBeijing Research Institute of Automation for Machinery Industry, Beijing, People's Republic of China.
Qian ZhuShandong University, Weihai, People's Republic of China.
Changlong JinShandong University, Weihai, People's Republic of China. cljin@sdu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rapid advancements in deep neural network models have significantly enhanced the ability to extract features from microbial sequence data, which is critical for addressing biological challenges. However, the scarcity and complexity of labeled microbial data pose substantial difficulties for supervised learning approaches. To address these issues, we propose DNASimCLR, an unsupervised framework designed for efficient gene sequence data feature extraction.

resultsDNASimCLR leverages convolutional neural networks and the SimCLR framework, based on contrastive learning, to extract intricate features from diverse microbial gene sequences. Pre-training was conducted on two classic large scale unlabelled datasets encompassing metagenomes and viral gene sequences. Subsequent classification tasks were performed by fine-tuning the pretrained model using the previously acquired model. Our experiments demonstrate that DNASimCLR is at least comparable to state-of-the-art techniques for gene sequence classification. For convolutional neural network-based approaches, DNASimCLR surpasses the latest existing methods, clearly establishing its superiority over the state-of-the-art CNN-based feature extraction techniques. Furthermore, the model exhibits superior performance across diverse tasks in analyzing biological sequence data, showcasing its robust adaptability.

conclusionsDNASimCLR represents a robust and database-agnostic solution for gene sequence classification. Its versatility allows it to perform well in scenarios involving novel or previously unseen gene sequences, making it a valuable tool for diverse applications in genomics.

Indexed as

Deep LearningMetagenomeNeural Networks, ComputerBiological sequence dataContrastive learningConvolutional neural networksRepresentation learningSequence classificationSimCLR

Identifiers

PMID39402441
PMCPMC11476100

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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.