E.g. An aligner (bowtie) has a list of common genome references that most users
could chose from, but some users will want to use their own reference sequence.
Currently the only way to support this seems to be by duplicating the tool.
Ideally, a user should be able to select from a dropdown of configured paths,
or, in some way be able to indicate 'other' and select a loaded file or enter a
path. The value from either method should go into option '-ref'.
Original issue reported on code.google.com by s.willi...@qfab.org on 19 Aug 2011 at 4:40
Original issue reported on code.google.com by
s.willi...@qfab.org
on 19 Aug 2011 at 4:40