can we generalize on behalf of users ? thought the whole point here is that the resource recommendations are based on user's genome size and read coverage (which we won't know beforehand right ?) Thinking in terms of a nf-core beginner user - I would like to use the rnaseq pipeline on a new genome say, axolotl for my reads with x coverage -> run test using one sample and then get optimized config based on that -> apply config & run for rest of samples