"Applied bioinformatics" is a course for Genetics Master Program at Genetics Department
-
Updated
Oct 12, 2023 - R
"Applied bioinformatics" is a course for Genetics Master Program at Genetics Department
This is a repository for a pipeline used to identify imprinted genes or allele specific expressions using Illumina next generation sequencing (NGS) platform. This repository contains a work in progress to identify imprinted genes in polyploid species.
R Shiny app encapsulating FilLT3r tool : https://doi.org/10.1186/s12859-022-04983-6
R Shiny app for germline genomic variants interpretation. The tool suite to deal with the underlying local structured database is provided here : https://github.com/clbenoit/GermlineVarDBTools
R Shiny app for somatic genomic variants interpretation. The tool suite to deal with the underlying local structured database is provided here : https://github.com/clbenoit/SomaVarDBTools
Add a description, image, and links to the dna-seq topic page so that developers can more easily learn about it.
To associate your repository with the dna-seq topic, visit your repo's landing page and select "manage topics."