Evidence map›Paper›PMID 40552980›Full record

ArticleGigaScience2025

PVGA: a precise viral genome assembler using an iterative alignment graph.

Zhi Song, Dehan Cai, Yanni Sun, Lusheng Wang

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Zhi SongDepartment of Computer Science, City University of Hong Kong, Kowloon, Hong Kong SAR (HKG), China.ORCID 0000-0001-9720-1084
Dehan CaiDepartment of Electrical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR (HKG), China.ORCID 0000-0002-8148-4574
Yanni SunDepartment of Electrical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR (HKG), China.ORCID 0000-0003-1373-8023
Lusheng WangDepartment of Computer Science, City University of Hong Kong, Kowloon, Hong Kong SAR (HKG), China.ORCID 0000-0002-4344-8791

Funding

GRF 11218821National Science Foundation 61972329
6 · The paper itself

Abstract

backgroundViral genome analysis is crucial for understanding virus evolution and mutation. Investigations into viral evolutionary dynamics and mutation patterns have garnered significant research attention since the outbreak of COVID-19. The basic structure of many virus genomes is highly conserved [1]. RNA viruses have high mutation rates, and single-nucleotide variations may induce substantial phenotypic alterations in terms of viral function and pathogenicity. Thus, special assembly methods are required for viral genome analysis.

resultPVGA starts with a reference genome and the sequencing reads. The first step in PVGA involves constructing an alignment graph based on a reference genome and the set of input sequencing reads. Then the optimal genomic path is determined through dynamic programming, maximizing the cumulative edge weights that reflect read support density across the alignment graph. The obtained path corresponds to a refined genome. Finally, we repeat the process by using the new reference genomes until no further improvement is possible. We evaluate PVGA's performance across both assembly and polishing tasks using simulated and real datasets, including both long reads and short reads. The experiments demonstrate that PVGA always outperforms popular existing programs in terms of the quality of assembly results, while the running time of our method is compatible to others. In particular, simulated Nanopore datasets show that our method can correctly report the true genomes with 0 mismatches and 0 indels.

conclusionsPVGA is a novel viral genome assembler that seamlessly integrates assembly and polishing into a unified workflow. Its design prioritizes high accuracy, enabling the detection of subtle genomic variations that can impact viral function and pathogenicity. By addressing the unique challenges of viral genome assembly, PVGA provides a reliable and precise solution for advancing our understanding of viral evolution and behavior.

Indexed as

Genome, ViralSARS-CoV-2SoftwareAlgorithmsComputational BiologyCOVID-19GenomicsHumansSequence Alignmentalignment graphgenome assembleriterative methodmaximum total weight pathvirus genome

Identifiers

PMID40552980
PMCPMC12206156

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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.