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1. CNVand CNVand Public

   A snakemake workflow to analyse and annotate copy number variants

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2. variant_visualization variant_visualization Public

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3. primertool primertool Public

   Streamlit app for generating primers for PCR/Sanger sequencing based on genomic variants. Demo available at https://primertool.simonmichau.de

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4. CNVizard CNVizard Public

   Browser-based tool for visualizing and analyzing germline copy number variants in genomic data.

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5. bulkRNASeq bulkRNASeq Public

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