Evidence map›Paper›PMID 38649300›Full record

ArticleGigaScience2024

IPEV: identification of prokaryotic and eukaryotic virus-derived sequences in virome using deep learning.

Hengchuang Yin, Shufang Wu, Jie Tan, Qian Guo, Mo Li, Jinyuan Guo, Yaqi Wang, Xiaoqing Jiang, Huaiqiu Zhu

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.8field-weighted citation impact, top 11% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Hengchuang YinDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-9561-7817
Shufang WuDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0001-7793-2509
Jie TanDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-5231-2124
Qian GuoDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-8622-8553
Mo LiDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-6496-9756
Jinyuan GuoDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0001-8218-5974
Yaqi WangDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-7261-4947
Xiaoqing JiangDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0001-7475-1630
Huaiqiu ZhuDepartment of Biomedical Engineering, College of Future Technology, and Center for Quantitative Biology, Peking University, Beijing 100871, China.ORCID 0000-0002-6376-218X
Peking University · CNGeorgia Institute of Technology · USChinese Academy of Sciences · CN

Funding

National Key Research and Development Program of China 2021YFC2300300National Natural Science Foundation of China 32070667
6 · The paper itself

Abstract

backgroundThe virome obtained through virus-like particle enrichment contains a mixture of prokaryotic and eukaryotic virus-derived fragments. Accurate identification and classification of these elements are crucial to understanding their roles and functions in microbial communities. However, the rapid mutation rates of viral genomes pose challenges in developing high-performance tools for classification, potentially limiting downstream analyses.

findingsWe present IPEV, a novel method to distinguish prokaryotic and eukaryotic viruses in viromes, with a 2-dimensional convolutional neural network combining trinucleotide pair relative distance and frequency. Cross-validation assessments of IPEV demonstrate its state-of-the-art precision, significantly improving the F1-score by approximately 22% on an independent test set compared to existing methods when query viruses share less than 30% sequence similarity with known viruses. Furthermore, IPEV outperforms other methods in accuracy on marine and gut virome samples based on annotations by sequence alignments. IPEV reduces runtime by at most 1,225 times compared to existing methods under the same computing configuration. We also utilized IPEV to analyze longitudinal samples and found that the gut virome exhibits a higher degree of temporal stability than previously observed in persistent personal viromes, providing novel insights into the resilience of the gut virome in individuals.

conclusionsIPEV is a high-performance, user-friendly tool that assists biologists in identifying and classifying prokaryotic and eukaryotic viruses within viromes. The tool is available at https://github.com/basehc/IPEV.

Indexed as

Deep LearningViromeVirusesComputational BiologyEukaryotaGenome, ViralHumansProkaryotic CellsSoftware

Identifiers

PMID38649300
PMCPMC11034026
OpenAlexW4395016580

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.