Dear Galaxy Developer,
where is the "history/workflow" file stored in the local machine?
Best regards
--
Yang Chen
Room 635, No.41 Building,320 Yueyang Road
Institute of Biochemistry and Cell Biology
Shanghai Institutes for Biological Sciences
Chinese Academy of Sciences
Shanghai,P.R.China
Post C
Dear Galaxy Developer,
where is the "history/workflow" file stored in the local machine?
I mean the real file store in the disk instead of browser access.
Thanks and Best regards
--
Yang Chen
Room 635, No.41 Building,320 Yueyang Road
Institute of Biochemistry and Cell Biology
Shanghai Institut
Dear Galaxy Developer,
where is the "history/workflow" flow stored in the local machine?
Best regards
--
Yang Chen
Room 635, No.41 Building,320 Yueyang Road
Institute of Biochemistry and Cell Biology
Shanghai Institutes for Biological Sciences
Chinese Academy of Sciences
Shanghai,P.R.China
P
Galaxy Team,
I would like to create a workflow by combining portions of two
different workflows. How do I do this in Galaxy?
Thanks,
Getiria Onsongo
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The Galaxy User list should be used for the discussion of
Galaxy analysis and other feat
On Mon, Mar 19, 2012 at 4:53 PM, Innocent Onsongo wrote:
> Galaxy Team,
>
> I would like to create a workflow by combining portions of two
> different workflows. How do I do this in Galaxy?
>
> Thanks,
> Getiria Onsongo
One outline solution is as follows:
(1) Start with an empty history.
(2) Upl
You forgot to CC the mailin list.
> On Mon, Mar 19, 2012 at 12:02 PM, Peter Cock
> wrote:
>> On Mon, Mar 19, 2012 at 4:53 PM, Innocent Onsongo wrote:
>>> Galaxy Team,
>>>
>>> I would like to create a workflow by combining portions of two
>>> different workflows. How do I do this in Galaxy?
>>>
Thanks. I was hoping there was an easier way e.g., selecting the two
workflows and exporting them into a workflow canvas. The workflows are
not too big so manually creating the workflows will probably be the
faster option for now.
On Mon, Mar 19, 2012 at 12:09 PM, Peter Cock wrote:
> You forgot t
Dear galaxy user
After running cuffdiff on my two samples (SAM files from bowtie)
i got a list with p and q values, and löast colum is saying abou significance
with P value, it seems like the comparison should be significant, but in Q
value is 1, and last coumn is saying not significant
any one
Hi there,
I have two questions regarding alignment using Bowtie:
1. Is there a way to set the Seed Length (-l) to the full length of each read
instead of using a single Seed Length for all reads?
2. When using m = -1 mode (Suppress all alignments for a read if more than n
reportable alignments
Hi,
I was wondering if there is any tool on Galaxy were I can obtain a table
with how many reads have been mapped to a given sample and to a given gene
(for example, use a Tophat output and use a GFF file to obtain the table).
I am using HTSeq to get it (htseq-count). There is also GenomicRanges
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