Vgas: A Viral Genome Annotation System

The in-depth study of viral genomes is of great help in many aspects, especially in the treatment of human diseases caused by viral infections. With the rapid accumulation of viral sequencing data, improved, or alternative gene-finding systems have become necessary to process and mine these data. In...

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Published inFrontiers in microbiology Vol. 10; p. 184
Main Authors Zhang, Kai-Yue, Gao, Yi-Zhou, Du, Meng-Ze, Liu, Shuo, Dong, Chuan, Guo, Feng-Biao
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 13.02.2019
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Summary:The in-depth study of viral genomes is of great help in many aspects, especially in the treatment of human diseases caused by viral infections. With the rapid accumulation of viral sequencing data, improved, or alternative gene-finding systems have become necessary to process and mine these data. In this article, we present Vgas, a system combining an method and a similarity-based method to automatically find viral genes and perform gene function annotation. Vgas was compared with existing programs, such as Prodigal, GeneMarkS, and Glimmer. Through testing 5,705 virus genomes downloaded from RefSeq, Vgas demonstrated its superiority with the highest average precision and recall (both indexes were 1% higher or more than the other programs); particularly for small virus genomes (≤ 10 kb), it showed significantly improved performance (precision was 6% higher, and recall was 2% higher). Moreover, Vgas presents an annotation module to provide functional information for predicted genes based on BLASTp alignment. This characteristic may be specifically useful in some cases. When combining Vgas with GeneMarkS and Prodigal, better prediction results could be obtained than with each of the three individual programs, suggesting that collaborative prediction using several different software programs is an alternative for gene prediction. Vgas is freely available at http://cefg.uestc.cn/vgas/ or http://121.48.162.133/vgas/. We hope that Vgas could be an alternative virus gene finder to annotate new genomes or reannotate existing genome.
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Reviewed by: Claire Bertelli, Lausanne University Hospital (CHUV), Switzerland; Vladislav Victorovich Khrustalev, Belarusian State Medical University, Belarus
These authors have contributed equally to this work
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
Edited by: Andrew S. Lang, Memorial University of Newfoundland, Canada
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2019.00184