Database Commons

a catalog of worldwide biological databases

The Papilloma Virus Episteme (PaVE) https://pave.niaid.nih.gov/ was initiated by NIAID in 2008 to provide a highly curated bioinformatic and knowledge resource for the papillomavirus scientific community. It rapidly became the fundamental and core resource for papillomavirus researchers and clinicians worldwide. Over time, the software infrastructure became severely outdated. In PaVE 2.0, the underlying libraries and hosting platform have been completely upgraded and rebuilt using Amazon Web Services (AWS) tools and automated CI/CD (continuous integration and deployment) pipelines for deployment of the application and data (now in AWS S3 cloud storage). PaVE 2.0 is hosted on three AWS ECS (elastic container service) using the NIAID Operations & Engineering Branch's Monarch tech stack and terraform. A new Celery queue supports longer running tasks. The framework is Python Flask with a JavaScript/JINJA template front end, and the database switched from MySQL to Neo4j. A Swagger API (Application Programming Interface) performs database queries, and executes jobs for BLAST, MAFFT, and the L1 typing tooland will allow future programmatic data access. All major tools such as BLAST, the L1 typing tool, genome locus viewer, phylogenetic tree generator, multiple sequence alignment, and protein structure viewer were modernized and enhanced to support more users. Multiple sequence alignment uses MAFFT instead of COBALT. The protein structure viewer was changed from Jmol to Mol*, the new embeddable viewer used by RCSB (Research Collaboratory for Structural Bioinformatics). In summary, PaVE 2.0 allows us to continue to provide this essential resource with an open-source framework that could be used as a template for molecular biology databases of other viruses.

The Papillomavirus Episteme (PaVE) is a database of curated papillomavirus genomic sequences, accompanied by web-based sequence analysis tools. This update describes the addition of major new features. The papillomavirus genomes within PaVE have been further annotated, and now includes the major spliced mRNA transcripts. Viral genes and transcripts can be visualized on both linear and circular genome browsers. Evolutionary relationships among PaVE reference protein sequences can be analysed using multiple sequence alignments and phylogenetic trees. To assist in viral discovery, PaVE offers a typing tool; a simplified algorithm to determine whether a newly sequenced virus is novel. PaVE also now contains an image library containing gross clinical and histopathological images of papillomavirus infected lesions. Database URL: https://pave.niaid.nih.gov/. Published by Oxford University Press on behalf of Nucleic Acids Research 2016. This work is written by (a) US Government employee(s) and is in the public domain in the US.

The goal of the Papillomavirus Episteme (PaVE) is to provide an integrated resource for the analysis of papillomavirus (PV) genome sequences and related information. The PaVE is a freely accessible, web-based tool (http://pave.niaid.nih.gov) created around a relational database, which enables storage, analysis and exchange of sequence information. From a design perspective, the PaVE adopts an Open Source software approach and stresses the integration and reuse of existing tools. Reference PV genome sequences have been extracted from publicly available databases and reannotated using a custom-created tool. To date, the PaVE contains 241 annotated PV genomes, 2245 genes and regions, 2004 protein sequences and 47 protein structures, which users can explore, analyze or download. The PaVE provides scientists with the data and tools needed to accelerate scientific progress for the study and treatment of diseases caused by PVs.