Package: ebGenotyping 2.0.1

ebGenotyping: Genotyping and SNP Detection using Next Generation Sequencing Data

Genotyping the population using next generation sequencing data is essentially important for the rare variant detection. In order to distinguish the genomic structural variation from sequencing error, we propose a statistical model which involves the genotype effect through a latent variable to depict the distribution of non-reference allele frequency data among different samples and different genome loci, while decomposing the sequencing error into sample effect and positional effect. An ECM algorithm is implemented to estimate the model parameters, and then the genotypes and SNPs are inferred based on the empirical Bayes method.

Authors:Na You <[email protected]> and Gongyi Huang<[email protected]>

ebGenotyping_2.0.1.tar.gz
ebGenotyping_2.0.1.zip(r-4.5)ebGenotyping_2.0.1.zip(r-4.4)ebGenotyping_2.0.1.zip(r-4.3)
ebGenotyping_2.0.1.tgz(r-4.5-any)ebGenotyping_2.0.1.tgz(r-4.4-any)ebGenotyping_2.0.1.tgz(r-4.3-any)
ebGenotyping_2.0.1.tar.gz(r-4.5-noble)ebGenotyping_2.0.1.tar.gz(r-4.4-noble)
ebGenotyping_2.0.1.tgz(r-4.4-emscripten)ebGenotyping_2.0.1.tgz(r-4.3-emscripten)
ebGenotyping.pdf |ebGenotyping.html
ebGenotyping/json (API)

# Install 'ebGenotyping' in R:
install.packages('ebGenotyping', repos = c('https://hmaoxian.r-universe.dev', 'https://cloud.r-project.org'))

On CRAN:

This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.

1.00 score 4 scripts 178 downloads 6 exports 0 dependencies

Last updated 9 years agofrom:994a6072f2. Checks:8 OK. Indexed: yes.

TargetResultLatest binary
Doc / VignettesOKFeb 13 2025
R-4.5-winOKFeb 13 2025
R-4.5-macOKFeb 13 2025
R-4.5-linuxOKFeb 13 2025
R-4.4-winOKFeb 13 2025
R-4.4-macOKFeb 13 2025
R-4.3-winOKFeb 13 2025
R-4.3-macOKFeb 13 2025

Exports:ecmesteplogitmstepmy.bisecrlogit

Dependencies: