Evidence map›Paper›PMID 40387494›Full record

ArticleBriefings in bioinformatics2025

VirNucPro: an identifier for the identification of viral short sequences using six-frame translation and large language models.

Jing Li, Jia Mi, Wei Lin, Fengjuan Tian, Jing Wan, Jingyang Gao, Yigang Tong

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 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. ADAPT: a programme for the advanced detection of AI-enabled pathogenic threats.Frontiers in bioengineering and biotechnology · 2026
    Article
  3. Review
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

7 authors.

Jing LiThe College of Information Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.ORCID 0000-0003-3060-2531
Jia MiThe College of Information Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.ORCID 0000-0002-9393-4288
Wei LinThe College of Life Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.
Fengjuan TianThe College of Life Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.
Jing WanThe College of Information Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.
Jingyang GaoThe College of Information Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.
Yigang TongThe College of Life Science and Technology, Beijing University of Chemical Technology, No. 15 North Third Ring East Road, Chaoyang District, Beijing 100029, China.

Funding

Capital Health Research and Development 2024-1G-4421
6 · The paper itself

Abstract

Viruses are ubiquitous in nature, yet our understanding of them remains limited. High-throughput sequencing technology facilitates the unbiased revelation of genetic composition in samples; however, viral sequences typically make up a small proportion of the entire sequencing data, making it challenging to accurately identify the few or fragmented viral sequences present in a sample. The limited features and information provided by short sequences result in insufficient resolution of viral sequences by existing models. Therefore, we propose a new model, VirNucPro, for short viral sequence identification. Based on a six-frame translation strategy and large language models, we combine nucleotide and amino acid sequence information to enhance feature extraction for short sequences, achieving high accuracy in identifying short viral sequences. Ablation experiments compared the contributions of nucleotide and amino acid sequence features to the model, confirming that the introduced amino acid features significantly contribute to the classification results. Our model outperforms others, such as GCNFrame, DeepVirFinder, DETIRE, and Virtifier, which have demonstrated good performance in identifying short viral sequences of 300 and 500 bp. Our model demonstrates excellent performance on carefully created real-world datasets. Additionally, it can scan for prophage regions within long bacterial fragments, offering a wide range of applications. The codes are available at: https://github.com/Li-Jing-1997/VirNucPro.

Indexed as

SoftwareVirusesAlgorithmsAmino Acid SequenceComputational BiologyHigh-Throughput Nucleotide SequencingLarge Language Modelslarge language modelssix-frame translationviral short sequences identifierVirNucPro

Identifiers

PMID40387494
PMCPMC12086996

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.