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App for the indexing, querying, comparison and benchmark of read depth and coverage of human genes, variants and genomic positions of health relevance, using anonymized human NGS data from available commercial exome capture probes against MANE Select transcripts.
Go library for parsing biological data formats and tool outputs from UniProt, PDB (Structure/Model/Chain/Residue/Atom - SMCRA), Pfam, DSSP, Fpocket and more. Plus: comparable position mappings!