Subject: | [galaxy-user] unable to import run or save-to-file published workflow after galaxy upgrade |
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Date: | Tue, 8 Oct 2013 23:44:32 +0000 |
From: | McCulloch, Alan <alan.mcculloch@agresearch.co.nz> |
To: | galaxy-user@lists.bx.psu.edu <galaxy-user@lists.bx.psu.edu> |
dear all,
we've just upgraded our Galaxy server
(Galaxy revision 7148:17d57db9a7c0, upgraded to revision
10422:a886bc3ae924 ), and
have found that an NGS training workflow
that one of us set up and published is no longer accessible -
we now get a stack trace
when we try to run it (screenshot attached)
; if we try to save to file, we "get page not found" from the
browser, but no errors
reported in web logs, or Galaxy log as far
as we can see
Is there any way we can recover the
workflow ?
How to avoid this happening in future
upgrades ? This time it is not a major problem, however we
would not want this to happen to
production workflows. Should we
save-to-file on all workflows as a precaution before an
upgrade ? (Would that help ? )
The workflow included steps as below.
Grateful for any suggestions.
Cheers
Alan McC
First Part : checking GC content
•Upload the sampling.fasta file or get it
from the shared data in Galaxy.
•Use geecee from EMBOSS
•Remove beginning (Text manipulation),
first line
•Convert as tabular (Text manipulation) or
cut (Text manipulation)
•Histogram (Graph/Display Data)on col2
•Compute data (Text manipulation) (data4
convert; col2>0.2)
•Count data (statistics on col3) If it is
worth it we can remove the sequences which have a too low GC
content
3
Second part : sequence length
•Compute Sequence length (FASTA
manipulation)
•Summary Statistics (Statistics)on col2
•Filter by length(FASTA manipulation) ; 800
•Line/world/character count(Text
manipulation)
•Blastn against fungi db : yeast, only one
hit to show (advanced options )
•Count the lines to know how many sequences
have a hit . (Text manipulation)
4
Bonus track : removing sequences with low
GC content
•Select (filter and sort) on data 6 where
matching = True
•FASTA-to-Tabular (FASTA manipulation) the
input file sampling.fasta (2 col for the title)
•Join two datasets(Join, Subtract and
Group) on the columns c1
•Tabular-to-FASTA (fasta manipulation) of
the previous results.
•You can see how many sequences you took
away (click on the dataset name in History) and it should
correspond to the number of True in Count .
5