Bhargava Reddy Morampalli

Thanks @yuukiiwa I initially ran the xpore without those filtering options and that was the output I was talking about where there are only a few positions. I tried again...

 More error code

What I usually do is basecall the data again with --fast5 out option during basecall. That way I have the fast5s with sequence information already in it. Then, I convert...