prompt$ hg help
>>
>> The "quick start" and "guide" at http://mercurial.selenic.com/ is a good
>> place for basic hg commands. A web search will return plenty of other
>> choices.
>>
>> This is the last email in this thread I think we shoul
ands. A web search will return plenty of other
>> choices.
>>
>> This is the last email in this thread I think we should send to both
>> lists - from here forward let's just cc to galaxy-...@bx.psu.edu for
>> follow-up and leave the user list off - no need to post to
ight now). So, otherwise the MAC install should be fine.
>
> Maybe this helps?
>
> Jen
> Galaxy team
>
> On 8/10/12 8:00 AM, Edward Turk wrote:
>> Both responses worked for checking python version, but trying to
>> download gave an error:
>>
>> Instal
.bx.psu.edu/Admin/Get%20Galaxy
>
>
> WRT checking the python version:
>
> just type 'python -V' on the command line, eg on my old MacBook:
>
> bash-3.2$ python -V
> Python 2.5.1
> bash-3.2$
>
>
> Hope this helps
> Regards, Hans
>
>
>
>
Hello,
Could someone provide instructions for installing galaxy on a Mac OS 10.7? The
instructions provided by galaxy start off by asking me to check my python
version, but I don't know how to do that. I figure someone has step-by-step
instructions or a screen cast?
Thank you,
Edward
___
want to conacatenate the fastq files (I assume that is what you
> mean) you can do that using the text manipulation tools: concatenate datasets
> tail-to-head.
> Good luck.
> Alex
>
>
> Van: galaxy-user-boun...@lists.bx.psu.edu
&g
Hi Galaxy Users,
Can FASTQ Databases be merged using Galaxy?
Thanks,
Edward
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org. Please keep all replies on t
Hello all,
I have used Tophat to map and now I want to filter out all reads that mapped to
the positive strand. Any help would be greatly appreciated.
Thanks,
Edward Turk
___
The Galaxy User list should be used for the discussion of
in Trackster ("Visualization" at Galaxy is a great
> alternative.
>
> Hopefully this helps,
>
> Jen
> Galaxy team
>
>
> On 6/24/11 8:40 AM, Edward Turk wrote:
>> For yeast analysis I use the following assembly: S. cerevisiae June 2008
>> (SGD/sacCer2) (sa
For yeast analysis I use the following assembly: S. cerevisiae June 2008
(SGD/sacCer2) (sacCer2). Recently a new yeast genome has appeared as an option
in Galaxy: S. cerevisae str. S288C (Saccharomyces_cerevisiae_S288C_SGD2010). Is
this an update to sacCer2? Where is it coming from? I don't see
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