Hi,
I'd find it extremely useful to be able to monitor/remember which reads have been corrected for paired-end overlap. I find this feature particularly useful for sequencing experiments from FFPE-extracted DNA/RNA, but I need to be able to see exactly which reads have been corrected, as well as how many.
Thanks!
Ale
Hi,
I'd find it extremely useful to be able to monitor/remember which reads have been corrected for paired-end overlap. I find this feature particularly useful for sequencing experiments from FFPE-extracted DNA/RNA, but I need to be able to see exactly which reads have been corrected, as well as how many.
Thanks!
Ale