rfaRm
rfaRm provides programmatic client-side access to the Rfam database for retrieval of non-coding RNA (ncRNA) family data, including member sequences, multiple sequence alignments, secondary structures, and covariance models, to support genomic analyses.
Key Features:
- Database search capabilities: Search the Rfam database using keywords or specific sequences to locate RNA families and associated metadata.
- Data retrieval: Retrieve member sequences, multiple sequence alignments, secondary structures, and covariance models for Rfam families.
- Programmatic access: Provide programmatic R-based access to Rfam data for integration into computational genomic workflows.
Scientific Applications:
- Genomic research integration: Incorporate ncRNA family data into broader genomic studies to investigate RNA functions and interactions.
- SARS-CoV-2 genome analysis: Apply Rfam-based ncRNA searches and data retrieval to analyze ncRNA elements in the SARS-CoV-2 genome.
Methodology:
rfaRm interfaces directly with the Rfam database to execute searches and retrieve data programmatically.
Topics
Details
- Tool Type:
- command-line tool, library
- Programming Languages:
- R
- Added:
- 3/19/2021
- Last Updated:
- 4/2/2021
Operations
Publications
Sellés Vidal L, Ayala R, Stan G, Ledesma-Amaro R. rfaRm: An R client-side interface to facilitate the analysis of the Rfam database of RNA families. PLOS ONE. 2021;16(1):e0245280. doi:10.1371/journal.pone.0245280. PMID:33449976. PMCID:PMC7810343.
PMID: 33449976
PMCID: PMC7810343
Funding: - Biotechnology and Biological Sciences Research Council: BB/T011408/1
- Engineering and Physical Sciences Research Council: EP/M002187/1