https://www.biorxiv.org/content/10.1101/2025.11.07.686952v1
according to preprint; it looks to:
-Perform better at finding simulated variants (with simulated reads), particularly when using PacBio Hifi
-Call more variants in line with QUAST when using reference
However currently the information on the tool is extremely limited (no indication of the output)
Installation looks annoying to integrate
and no idea if there is a score; or perhaps will have to recalculate scores based on the number of miss-assemblies detected
https://www.biorxiv.org/content/10.1101/2025.11.07.686952v1
according to preprint; it looks to:
-Perform better at finding simulated variants (with simulated reads), particularly when using PacBio Hifi
-Call more variants in line with QUAST when using reference
However currently the information on the tool is extremely limited (no indication of the output)
Installation looks annoying to integrate
and no idea if there is a score; or perhaps will have to recalculate scores based on the number of miss-assemblies detected