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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>.
| Version: | 1.0.1 |
| Published: | 2024-01-25 |
| DOI: | 10.32614/CRAN.package.SNVLFDR |
| Author: | Ali Karimnezhad [aut, cre, ctb] |
| Maintainer: | Ali Karimnezhad <ali.karimnezhad at gmail.com> |
| License: | GPL (≥ 3) |
| NeedsCompilation: | no |
| Materials: | README |
| CRAN checks: | SNVLFDR results |
| Reference manual: | SNVLFDR.pdf |
| Package source: | SNVLFDR_1.0.1.tar.gz |
| Windows binaries: | r-devel: SNVLFDR_1.0.1.zip, r-release: SNVLFDR_1.0.1.zip, r-oldrel: SNVLFDR_1.0.1.zip |
| macOS binaries: | r-release (arm64): SNVLFDR_1.0.1.tgz, r-oldrel (arm64): SNVLFDR_1.0.1.tgz, r-release (x86_64): SNVLFDR_1.0.1.tgz, r-oldrel (x86_64): SNVLFDR_1.0.1.tgz |
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These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.