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Forked from xbrowse/minimal_representation
Convert genetic variants to minimal representation
Analysis of the penetrance of missense variants and tolerability of loss-of-function variants in PRNP
Evaluating potential drug targets through human loss-of-function genetic variation
Comparison of callability in whole genomes vs. whole exoms
Scripts dealing with various aspects of next-gen sequence data. QC, CNVs, etc
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