DNA is sequenced to depths targeted to maximize diversity capture using a combination of Oxford Nanopore and Illumina for long and short reads, respectively, allowing for the generation of high quality and high contiguity genomic assemblies.
The combination of ONT and Illumina is great - I wondered if you have found a tradeoff of trying to maximise finding diversity, i.e., reads that have differences, but also minimize retaining reads with sequencing errors that look artificially dissimilar. Presumably, walking the line between the two is critical to not over-inflating diversity estimates and retaining only confident 'true' standing diversity - I would love to know more about how you navigate this!