Compatibility with bed file is provided that contains 1,000,000 random positions on the hg19/GRCh37 human genome reference ?

[ElisouG]

Hi nanosv team, Is your tool compatible with human genome version hg38/GRCh378 ? If yes, did you produce the bed file for compute the coverage distribution with this genome and could you share it ? If not, how can I generate it ? Kind regards, Elise