Hello All,
I have a minimap2 aligned .paf file of two genomes. This paf file was used to identify structural variant (SVs) shared between these genomes. How do I use this paf file alone for a precise detection of SV breakpoints?
Thank you for your time and feedback in advance.
Regards,
B
I have a minimap2 aligned .paf file of two genomes. This paf file was used to identify structural variant (SVs) shared between these genomes. How do I use this paf file alone for a precise detection of SV breakpoints?
Thank you for your time and feedback in advance.
Regards,
B