This is control panel for nanomonsv software, which is expected to exclude many false positives as well as improve computational cost. This is made by aligning 30 Nanopore sequencing data from Human Pangenome Reference Consortium to the GRCh38 reference genome (obtained from here) with minimap2 version 2.24. When you use these control panels and publish, do not forget to credit to HPRC!

{"references": ["Shiraishi et al., Precise characterization of somatic structural variations and mobile element insertions from paired long-read sequencing data with nanomonsv, bioRxiv, 2020."]}