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SNVLFDR  

Empirical Bayes Single Nucleotide Variant Calling
View on CRAN: Click here


Download and install SNVLFDR package within the R console
Install from CRAN:
install.packages("SNVLFDR")

Install from Github:
library("remotes")
install_github("cran/SNVLFDR")

Install by package version:
library("remotes")
install_version("SNVLFDR", "1.0.1")



Attach the package and use:
library("SNVLFDR")
Maintained by
Ali Karimnezhad
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2024-01-25
Latest Update: 2024-01-25
Description:
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>.
How to cite:
Ali Karimnezhad (2024). SNVLFDR: Empirical Bayes Single Nucleotide Variant Calling. R package version 1.0.1, https://cran.r-project.org/web/packages/SNVLFDR. Accessed 06 Oct. 2024.
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Complete documentation for SNVLFDR
Functions, R codes and Examples using the SNVLFDR R package
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