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1. SavvySuite SavvySuite Public

   Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes

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2. snippets snippets Public

   Small snippets of useful code

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3. MNV-test-data MNV-test-data Public

   A BAM file containins five MNVs (Multiple Nucleotide Variants) for the purposes of testing bioinformatics pipelines.

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4. NGS-LIMS NGS-LIMS Public

   web app development to display variant and coverage data from NGS analysis

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5. intro_to_WDL intro_to_WDL Public

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6. virtual_panel_parser virtual_panel_parser Public

   Selects possible pathogenic variants from an Alamut output and a gene list

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