At the moment we print a bed-like file that has onlt the probability of mutation not the mutant sample or its genotype. It might make sense to invoke something like what we have in the post-processor (#3) when a site meets the probability cut so we can write a lot more information about each site.
We should decide on one...
At the moment we print a bed-like file that has onlt the probability of mutation not the mutant sample or its genotype. It might make sense to invoke something like what we have in the post-processor (#3) when a site meets the probability cut so we can write a lot more information about each site.