Pugh Lab
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Pugh Lab
bamgineer
37
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Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
VisCap
22
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VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number variants (CNVs) from targeted next-generation sequencing data. Fo...
ConsensusCruncher
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ConsensusCruncher is a tool that suppresses errors in next-generation sequencing data by using unique molecular identifiers (UMIs) to amalgamate reads derived from the same DNA template into a consens...