2020
DOI: 10.1093/ve/veaa068
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PuMA: A papillomavirus genome annotation tool

Abstract: High-throughput sequencing technologies provide unprecedented power to identify novel viruses from a wide variety of (environmental) samples. The field of ‘viral metagenomics’ has dramatically expanded our understanding of viral diversity. Viral metagenomic approaches imply that many novel viruses will not be described by researchers who are experts on (the genomic organization of) that virus family. We have developed the papillomavirus annotation tool (PuMA) to provide researchers with a convenient and reprod… Show more

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Cited by 12 publications
(11 citation statements)
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“…We determined the genomes of two novel circular dsDNA viruses using a metagenomics approach. The open reading frames (ORFs) of these putative new viruses were identified using PuMA ( 150 ). This analysis identified the typical papillomavirus open reading frames (E6, E7, E1, E2, L1, and L2) and the spliced E1^E4 and E8^E2 mRNAs.…”
Section: Resultsmentioning
confidence: 99%
“…We determined the genomes of two novel circular dsDNA viruses using a metagenomics approach. The open reading frames (ORFs) of these putative new viruses were identified using PuMA ( 150 ). This analysis identified the typical papillomavirus open reading frames (E6, E7, E1, E2, L1, and L2) and the spliced E1^E4 and E8^E2 mRNAs.…”
Section: Resultsmentioning
confidence: 99%
“…We also identified two spliced products, E8^E2 and E1^E4 in two of the genomes. The splice donor and acceptor sequences were identified by homology in the PuMA tool [ 22 ]. The upstream regulatory regions (URRs) range in size from 504 to 613 bp.…”
Section: Resultsmentioning
confidence: 99%
“…The 7307-bp contig was annotated using the PuMA pipeline [ 22 ]. This sequence corresponded to a full papillomavirus genome encoding L1, L2, E1, E2, E6 and E7, in addition to two spliced products (E1^E4 and E8^E2).…”
Section: Methodsmentioning
confidence: 99%
“…They may, however, result in incorrect functional annotations [ 52 ]. Annotating genomes correctly is critical for our knowledge and use of functional gene diversity [ 53 , 54 ]. In order to confirm the accuracy of the gene annotations, structural analysis or assessment of expression level is usually necessary [ 55 ].…”
Section: Discussionmentioning
confidence: 99%