visual analysis of your VCF files
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Updated
Dec 3, 2022 - R
visual analysis of your VCF files
R tools to interact with hap.py output
Reporting toolbox for happy output
Tumor in normal detection
Bioinformatics pipelines developed while working at the dept of Obs & Gynae
Tools for analyzing UMIErrorCorrect output
Management flow using PBS system to analyze sequencing data from Illumina Novaseq6000
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
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
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