WisecondorFF: A whole-genome sequencing based copy number variation detection tool. WisecondorFF builds further upon WisecondorX by integrating fragment size inferred from paired-end reads and combining these data with the within-sample comparison based on genome read coverage.
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This project has been set up using PyScaffold 4.3.1. For details and usage information on PyScaffold see https://pyscaffold.org/.