rasusa
rasusa randomly subsamples sequencing reads to a user-specified coverage for analyses that require reduced dataset size while preserving representativeness.
Key Features:
- Unbiased subsampling: Produces random subsamples intended to be representative of the input read set.
- Specified coverage: Subsamples reads to achieve a user-defined sequencing coverage level.
- Sequencing-technology compatibility: Operates across different sequencing technologies to support diverse genomic studies.
Scientific Applications:
- Computational resource reduction: Reduces dataset size to accommodate limited computational resources while maintaining representativeness.
- Pilot and preliminary analyses: Provides smaller representative datasets for preliminary experiments and parameter tuning.
- Large-dataset reduction: Lowers data volume for analyses of large sequencing projects without losing significant information content.
Methodology:
Randomly subsamples sequencing reads to reach a user-specified coverage, producing an unbiased representative subset of the input reads.
Topics
Details
- License:
- MIT
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Added:
- 4/22/2021
- Last Updated:
- 11/6/2024
Operations
Publications
Hall M. Rasusa: Randomly subsample sequencing reads to a specified coverage. Journal of Open Source Software. 2022;7(69):3941. doi:10.21105/joss.03941.
DOI: 10.21105/joss.03941
Documentation
Installation instructions
https://github.com/GlobalPathogenAnalysisService/read-it-and-keep/blob/main/README.md