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>.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
1.0.1 |
rolling linux/jammy R-4.5 | SNVLFDR_1.0.1.tar.gz |
123.1 KiB |
1.0.1 |
rolling linux/noble R-4.5 | SNVLFDR_1.0.1.tar.gz |
123.1 KiB |
1.0.1 |
rolling source/ R- | SNVLFDR_1.0.1.tar.gz |
65.6 KiB |
1.0.1 |
latest linux/jammy R-4.5 | SNVLFDR_1.0.1.tar.gz |
123.1 KiB |
1.0.1 |
latest linux/noble R-4.5 | SNVLFDR_1.0.1.tar.gz |
123.1 KiB |
1.0.1 |
latest source/ R- | SNVLFDR_1.0.1.tar.gz |
65.6 KiB |
1.0.1 |
2026-04-26 source/ R- | SNVLFDR_1.0.1.tar.gz |
65.6 KiB |
1.0.1 |
2026-04-23 source/ R- | SNVLFDR_1.0.1.tar.gz |
65.6 KiB |
1.0.1 |
2026-04-09 windows/windows R-4.5 | SNVLFDR_1.0.1.zip |
119.5 KiB |
1.0.1 |
2025-04-20 source/ R- | SNVLFDR_1.0.1.tar.gz |
65.6 KiB |