SNVLFDR
Empirical Bayes Single Nucleotide Variant Calling
Identifies single nucleotide variants in next-generation sequencing data by estimating their local false discovery rates. For more details, see Karimnezhad, A. and Perkins, T. J. (2024) doi:10.1038/s41598-024-51958-z.
- Version1.0.1
- R versionunknown
- LicenseGPL (≥ 3)
- Needs compilation?No
- Last release01/25/2024
Documentation
Team
Ali Karimnezhad
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