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CoNVaDING
Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV) detection in high coverage next-generation sequencing (NGS) data
GNU Lesser General Public License v3.0
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Fixed bug introduced in previous version
#26
Closed
freerkvandijk
closed
7 years ago
freerkvandijk
commented
7 years ago
Start positions of events in shortlist are now calculated properly