Move type: paired-end to top-level sequencing-read-type or some other similar name. Could also optionally have it per normal/tumor/RNA in case those end up being different for some reason, but seem unnecessary to have it for each "fragment".
Also, anything we do to hide the term "fragment" from the user would be good, since it's confusing the context of sequencing.
Move
type: paired-end
to top-levelsequencing-read-type
or some other similar name. Could also optionally have it per normal/tumor/RNA in case those end up being different for some reason, but seem unnecessary to have it for each "fragment".Also, anything we do to hide the term "fragment" from the user would be good, since it's confusing the context of sequencing.
One possibility, instead of
have:
or: