virMine 2.0
virMine 2.0 identifies viral sequences within complex microbial community sequencing reads by excluding nonviral data and scoring remaining sequences for relatedness to known viral elements.
Key Features:
- Exclusion filtering: Employs an exclusion technique to filter out nonviral data from sequencing reads.
- Relatedness scoring: Scores remaining sequences based on their relatedness to known viral elements rather than relying exclusively on direct sequence homology.
- Reduced homology dependency: Decreases reliance on traditional homology identification methods to accommodate viral evolutionary variability.
- Focus on viral candidates: Concentrates computational resources on sequences identified as potential viral elements to enhance detection specificity.
- Applicability to diverse viruses: Broadens detection applicability to viruses with limited or no existing reference sequences by using relatedness-based scoring.
Scientific Applications:
- Viral diversity surveys: Enables exploration of viral diversity in environmental and metagenomic samples.
- Virus–host interaction studies: Supports investigation of virus-host interactions within microbial communities.
- Ecosystem dynamics research: Facilitates study of the roles of viruses in ecosystem and community dynamics.
- Metagenomic viral identification: Assists in distinguishing viral sequences from bacterial and archaeal DNA in comprehensive metagenomic datasets.
Methodology:
Applies an exclusion technique to remove nonviral sequencing reads and then scores the remaining sequences for relatedness to known viral elements, reducing dependence on direct sequence homology.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python, Shell
- Added:
- 8/13/2022
- Last Updated:
- 8/13/2022
Operations
Publications
Johnson G, Putonti C. virMine 2.0: Identifying Viral Sequences in Microbial Communities. Microbiology Resource Announcements. 2022;11(5). doi:10.1128/mra.00107-22. PMID:35499341. PMCID:PMC9119091.
DOI: 10.1128/MRA.00107-22
PMID: 35499341
PMCID: PMC9119091
Funding: - National Science Foundation: 1661357