Re: [galaxy-user] Quality report

2013-11-06 Thread James Taylor
On Wed, Nov 6, 2013 at 12:54 PM, Benjamin Osei-agyeman 
benjy_o...@yahoo.co.uk wrote:

 The report was obtained after running fastqc on my data. However after
 looking at the report statistics, the
 Quality is not good in the Per Base Sequence Quality and there is a
 difference between the mean and median at each cycle. How can the quality
 be improved?


Is the quality poor across the entire read, or just at one end? You can
improve overall quality in two ways. By filtering out lower quality reads
(the Filter by Quality tool or Filter FASTQ tool) or by trimming a portion
of the reads (the FASTQ trimmer tool).

It is important to understand that these tools work by throwing away data,
you can't improve the overall quality of reads you already have. The FASTQC
tool is telling you about the quality of your sequencing experiment. The
only way to improve the overall quality is to do the experiment again.


 And why is there a difference between the mean and median in the fastqc
 report at each cycle?


It means your quality score distribution is skewed. This is not necessarily
a concern.


--
James Taylor, Associate Professor, Biology/CS, Emory University
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Re: [galaxy-user] Need your helps about Galaxy

2013-09-24 Thread James Taylor
As I said before, there is no easy way to do this. You just need to
dump the old database and load into the new database. I would suggest
making a copy of the old database with a current version of Galaxy.
The migration scripts will then bring it up to date so you will have
identical schemas. You should then be able to dump and load easily
enough, you will just need to move the dump file between servers.

--
James Taylor, Associate Professor, Biology/CS, Emory University


On Mon, Sep 23, 2013 at 3:36 PM, Lei Yan leiyan2...@gmail.com wrote:
 Dear Dannon,

 I built a new cloud Galaxy instance today.
 Would you please tell me how to transfer given accounts from an old Galaxy
 to this new one?
 This is old Galaxy: http://galaxylocal.genenetwork.org:8080/
 This is new Galaxy: http://galaxyclass.genenetwork.org/
 Thanks a lot.


 Lei Yan
 Center for Integrative and Translational Genomics
 UTHSC

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Re: [galaxy-user] Secure file upload gateway for Galaxy

2013-09-24 Thread James Taylor
Galaxy's FTP support uses ProFTPD, which has modules for both TLS
(FTPS) and SFTP.

--
James Taylor, Associate Professor, Biology/CS, Emory University


On Tue, Sep 24, 2013 at 7:58 AM, Georgios Magklaras
georg...@biotek.uio.no wrote:
 Hi,

 Our team at the University of Oslo is building a Life Science Portal
 based on Galaxy. We operate several standalone instances and we have the
 necessary sysadmin experience, but we really need to implement a more
 secure file upload mechanism than FTP (we do not like to send cleartext
 password credentials in the open ), and we understand that Galaxy does
 not integrate an upload method other than FTP with reference to this
 screencast:

 http://screencast.g2.bx.psu.edu/quickie_17_ftp_upload/flow.html


 One possible solution for this is to setup an SFTP upload server with a
 huge scratch space, that runs the SFTP upload gateway on one end and an
 IP restricted FTP server on the other, so that users can then
 upload/index the SFTP uploaded data into their Galaxy session via the
 URL upload field. This two step process might be a bit cumbersome for
 some of our users and we are looking for ways to simplify it.

 Do you have best recipes for SFTP/Aspera upload gateway integration to
 Galaxy? We would welcome advise on that matter.

 GM


 Best regards,

 --
 --
 George Magklaras PhD
 RHCE no: 805008309135525

 Head of IT/Senior Systems Engineer
 Biotechnology Center of Oslo and
 the Norwegian Center for Molecular Medicine/
 Vitenskapelig Databehandling (VD) -
 Research Computing Services - USIT

 EMBnet TMPC Chair

 http://folk.uio.no/georgios
 http://www.uio.no/english/services/it/research/hpc/abel/

 Tel: +47 22840535

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Re: [galaxy-user] How do I add Ray to Galaxy Central in the tool shed ?

2013-06-06 Thread James Taylor
 I want to add Ray (a scalable de novo assembler for genomes and metagenomes)
 to Galaxy.

And I really want you to do this!

 I will also have to write a wrapper for Ray to prepare the command line from
 the options provided by the
 Galaxy API.


 But where is stored the executable (in my case, where is sdtored Ray) ?

 Does Galaxy include the specs to build all the tools available in
 Galaxy-Central ?

No, we are gradually moving all the tools out of galaxy-central into
the Tool Shed. You probably want to look at this page:

  
http://wiki.galaxyproject.org/ToolShedToolFeatures#Automatic_third-party_tool_dependency_installation_and_compilation_with_installed_repositories

Which describes how you can add a recipe to the toolshed that will
install the Ray binaries.
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Re: [galaxy-user] How to share an history with a SPECIFIC user ?

2013-06-03 Thread James Taylor
Sarah, when you share with a specfic user, it will not show up under
the Shared Data section since that is only for published items. The
person you share it with should see it under Histories Shared with
me which is in the History options menu:

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Mon, Jun 3, 2013 at 11:22 AM, Sarah Maman
sarah.ma...@toulouse.inra.fr wrote:
 Hello Jennifer,

 I would like to share only with a specific user but when I use the meth 3
 with the email address into last section, my history is not shared.
 I need to publish AND share with a mail , in order to see my history in
 shared data .
 It seems to be a bug ?

 Thanks in advance,
 Sarah

 Jennifer Jackson a écrit :

 Hello Sarah,

 On the history menu's share or publish page, there are three ways to share,
 one section per method:

 1 - generate a share link. this can be share with one or more users,
 account holders or not
 2 - publish the history - this places it in the list of all Shared
 Histories where everyone using that server can see it
 3 - share with just a user by entering in their email address into last
 section

 Hopefully this helps,

 Jen
 Galaxy team

 On 6/3/13 6:58 AM, Sarah Maman wrote:

 Hello,

 My question is about sharing histories with a specific user.
 The share is not effective for a specific one but for all users logged in
 our local instance.

 Could you please help me ?

 Thank you in advance,
 Sarah

 --
   --*--
 Sarah Maman
 INRA - LGC - SIGENAE
 http://www.sigenae.org/
 Chemin de Borde-Rouge - Auzeville - BP 52627
 31326 Castanet-Tolosan cedex - FRANCE
 Tel:   +33(0)5.61.28.57.08
 Fax:   +33(0)5.61.28.57.53
  --*--



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 --
 Jennifer Hillman-Jackson
 Galaxy Support and Training
 http://galaxyproject.org



 --
   --*--
 Sarah Maman
 INRA - LGC - SIGENAE
 http://www.sigenae.org/
 Chemin de Borde-Rouge - Auzeville - BP 52627
 31326 Castanet-Tolosan cedex - FRANCE
 Tel:   +33(0)5.61.28.57.08
 Fax:   +33(0)5.61.28.57.53
  --*--


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Re: [galaxy-user] Unable to use FASTQ tool on Main over several days

2013-05-24 Thread James Taylor
Hi, could you be more specific. Name one or two specific tools that
are not working. Also, when does the error occur, after submitting the
job or before loading the tool?

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Fri, May 24, 2013 at 10:31 AM, Eduardo Fox ofoxo...@gmail.com wrote:
 Please, I have been unable to use any of the tools under FASTQ Tools
 for the last 4 days. I keep getting an error message with codes, for
 instance GURU MEDITATION: #376b73ae417d41f3a7c2088770e13b8f.

 Is this part of the platform down for some reason?

 Best wishes and thanks,

 E. Fox
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Re: [galaxy-user] problem uploading txt data

2013-05-13 Thread James Taylor
Are the first four lines of your file deliberately whitespace? This
will definitely cause problems for file type detection (it is not a
valid TSV file as is).

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Sun, May 12, 2013 at 10:52 AM, Chunyu Liu liuc...@gmail.com wrote:
 hi,
 I had an odd problem today, seems not a problem before:
 I am trying to upload a simple tab-delimited text file into galaxy,
 but it kept telling me:
 empty
 format: txt, database: hg19
 The uploaded binary file contains inappropriate content

 Also, showed filesize as 0 bytes.

 I tried Unix format, DOS format. It is a very small data, only 348 bytes.
 4 rows, as attached.

 What is WRONG?

 Thanks!

 Chunyu

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Re: [galaxy-user] ImportError: Unable to run arch-specific checks

2013-04-25 Thread James Taylor
Since you have isolated the problem to running on ceph, I'm not sure
there is much help we can offer. My understanding is that the posix
filesystem part of ceph (as opposed to the object store) is still in
development and could have bugs.

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Thu, Apr 25, 2013 at 7:35 AM, Shun Liang shun.li...@cruk.cam.ac.uk wrote:
 Dear Galaxy Developers,

 Here is some more information about the environment I am trying to install
 Galaxy on. I am using Ubuntu 12.10 on armv7l architecture. I encountered the
 Import Error problem when I was running Galaxy on the Ceph file system. This
 is how the Ceph file system is mounted on the machine:

 galaxy@arm01-25:~$ mount | grep ceph
 10.20.232.4,10.20.232.8,10.20.232.12,10.20.232.16,10.20.232.20:/ on
 /mnt/ceph type ceph (name=admin,key=client.admin)

 I have later tried to install and run Galaxy on the same machine but on a
 different directory which is within the EXT4 file system  mounted on the
 hard drive. Galaxy runs on that directory without any problem.

 I hope this gives some clue to you to solve the problem.

 Many thanks,


 Shun

 
 From: galaxy-user-boun...@lists.bx.psu.edu
 [galaxy-user-boun...@lists.bx.psu.edu] on behalf of Shun Liang
 [shun.li...@cruk.cam.ac.uk]
 Sent: 24 April 2013 14:56
 To: galaxy-u...@bx.psu.edu
 Subject: [galaxy-user] ImportError: Unable to run arch-specific checks

 Dear Galaxy Developers,

 I am trying to run Galaxy on ARM architecture. I am able to scramble the
 eggs locally. However, I am unable to run Galaxy on my machine as run.sh
 gives an error after some initialization steps:

 galaxy@arm01-48:/mnt/ceph/galaxy/galaxy-dist$ ./run.sh
 Initializing datatypes_conf.xml from datatypes_conf.xml.sample
 Initializing external_service_types_conf.xml from
 external_service_types_conf.xml.sample
 Initializing migrated_tools_conf.xml from migrated_tools_conf.xml.sample
 Initializing reports_wsgi.ini from reports_wsgi.ini.sample
 Initializing shed_tool_conf.xml from shed_tool_conf.xml.sample
 Initializing tool_conf.xml from tool_conf.xml.sample
 Initializing shed_tool_data_table_conf.xml from
 shed_tool_data_table_conf.xml.sample
 Initializing tool_data_table_conf.xml from tool_data_table_conf.xml.sample
 Initializing tool_sheds_conf.xml from tool_sheds_conf.xml.sample
 Initializing data_manager_conf.xml from data_manager_conf.xml.sample
 Initializing shed_data_manager_conf.xml from
 shed_data_manager_conf.xml.sample
 Initializing openid_conf.xml from openid_conf.xml.sample
 Initializing tool-data/shared/ncbi/builds.txt from builds.txt.sample
 Initializing tool-data/shared/ensembl/builds.txt from builds.txt.sample
 Initializing tool-data/shared/ucsc/builds.txt from builds.txt.sample
 Initializing tool-data/shared/ucsc/publicbuilds.txt from
 publicbuilds.txt.sample
 Initializing tool-data/shared/igv/igv_build_sites.txt from
 igv_build_sites.txt.sample
 Initializing tool-data/shared/rviewer/rviewer_build_sites.txt from
 rviewer_build_sites.txt.sample
 Initializing tool-data/add_scores.loc from add_scores.loc.sample
 Initializing tool-data/alignseq.loc from alignseq.loc.sample
 Initializing tool-data/all_fasta.loc from all_fasta.loc.sample
 Initializing tool-data/annotation_profiler_options.xml from
 annotation_profiler_options.xml.sample
 Initializing tool-data/annotation_profiler_valid_builds.txt from
 annotation_profiler_valid_builds.txt.sample
 Initializing tool-data/bfast_indexes.loc from bfast_indexes.loc.sample
 Initializing tool-data/binned_scores.loc from binned_scores.loc.sample
 Initializing tool-data/blastdb.loc from blastdb.loc.sample
 Initializing tool-data/blastdb_p.loc from blastdb_p.loc.sample
 Initializing tool-data/bowtie2_indices.loc from bowtie2_indices.loc.sample
 Initializing tool-data/ccat_configurations.loc from
 ccat_configurations.loc.sample
 Initializing tool-data/codingSnps.loc from codingSnps.loc.sample
 Initializing tool-data/encode_datasets.loc from encode_datasets.loc.sample
 Initializing tool-data/faseq.loc from faseq.loc.sample
 Initializing tool-data/funDo.loc from funDo.loc.sample
 Initializing tool-data/gatk_annotations.txt from gatk_annotations.txt.sample
 Initializing tool-data/gatk_sorted_picard_index.loc from
 gatk_sorted_picard_index.loc.sample
 Initializing tool-data/liftOver.loc from liftOver.loc.sample
 Initializing tool-data/maf_index.loc from maf_index.loc.sample
 Initializing tool-data/maf_pairwise.loc from maf_pairwise.loc.sample
 Initializing tool-data/microbial_data.loc from microbial_data.loc.sample
 Initializing tool-data/mosaik_index.loc from mosaik_index.loc.sample
 Initializing tool-data/ngs_sim_fasta.loc from ngs_sim_fasta.loc.sample
 Initializing tool-data/perm_base_index.loc from perm_base_index.loc.sample
 Initializing tool-data/perm_color_index.loc from perm_color_index.loc.sample
 Initializing tool-data/phastOdds.loc from phastOdds.loc.sample
 Initializing tool-data/picard_index.loc

Re: [galaxy-user] glitch in .wig visualization in trackster?

2013-03-27 Thread James Taylor
Hi Michael, sorry it took a while but we've figured out the root cause
of this issue and will be deploying a fix shortly. Thanks!

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Fri, Mar 22, 2013 at 4:20 PM, Michael Axtell mj...@psu.edu wrote:
 Hi everyone.

 I'm having an issue with a wiggle file.  I'm using Trackster on the
 public-main instance of Galaxy, with a custom genome build. My wiggle
 file fails to be shown. When added to the visualization using the 'add
 tracks' dialog, I see the usual hatched gray lines with the message
 processing data, this may take some time.  But then after a few
 minutes the track just goes to hatched gray lines with no messages,
 and the intensities are never displayed, nor is any error message (or
 any message at all, just stuck with the hatched gray lines).

 The .wig file has been extensively validated to conform to UCSC spec.
 In addition, the same file displays data just fine when loaded into
 Broad's IGV. So I'm confident it is formatted correctly.

 The custom genome is not a great one .. scaffolds not pseudomolecules,
 and there are many thousands of scaffolds in the assembly (scaffold
 N50 is 1.3M at scaffold 111 out of ~2,100 scaffolds; total length
 ~480M). If I slice my problematic wiggle file to only keep
 sub-sections of the data, sometimes it works.  I tested a number of
 such sub-slices, and some worked and some didn't, as below (the
 numbers refer to scaffold numbers in my custom genome):

 1-50 : worked
 1-100 : worked
 1-200 : worked
 1-300 : failed
 1-400 : failed
 1-500 : failed

 100-250 : worked
 200-300 : worked
 300-400 : worked
 500-600 : worked

 From the above, it seems possible the error is that Trackster just
 doesn't like wig files that exceed a certain number of
 chromosomes/scaffolds? Or some sort of data overload issue?

 Some other information: This custom genome build works fine on
 trackster to visualize several other datasets in gff, gff3, and bed
 format. In addition, the problem wiggle file is not so large .. the
 full file is only ~48M. It is a fixedStep file with span and step both
 equal to 100, and the data are relatively sparse.

 If anyone has a clue, let me know .. thanks!

 --
 Michael J. Axtell, Ph.D.
 Associate Professor
 Dept. of Biology
 Penn State University
 http://axtell-lab-psu.weebly.com
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Re: [galaxy-user] How to connect to private instance of galaxy from another computer

2013-03-14 Thread James Taylor
Yes, you will need to edit universe_wsgi.ini and change the entry for host
= (exactly what you need to do is documented in that file).


--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Wed, Mar 13, 2013 at 3:40 AM, Michael Milevskiy m.milevs...@uq.edu.auwrote:

  Dear Galaxy,

 ** **

 I am running an instance of Galaxy on my computer through localhost:8080/
 and am wondering if I can use this on my laptop? I basically don’t want to
 be at the computer at the same time and don’t want to upload files to and
 from my laptop but just use the galaxy interface to work with my data.

 ** **

 Regards,

 ** **

 Michael J.G. Milevskiy | BBiomedSc

 

 PhD Student
 School of Chemical and Molecular Biosciences
 Prof. Melissa Brown - Group Leader
 Molecular Biosciences Building 76-432
 The University of Queensland | (07) 3365 4635

 ** **

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Re: [galaxy-user] Installing Galaxy on ARM Architecture

2013-02-21 Thread James Taylor
You are definitely in uncharted territory with an arm server. Can you
try building just bx-python itself and let us know what the errors
are?

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Thu, Feb 21, 2013 at 11:03 AM, Shun Liang shun.li...@cruk.cam.ac.uk wrote:
 Hi,

 I am trying to install Galaxy on an ARMV7 architecture Linux server. I ran
 run.sh and failed because some of the python eggs could not be fetched. I
 then have a look at http://eggs.galaxyproject.org/; and I have realized
 there aren't any armv7 builds for those eggs.

 I then decided to build (or scramble) the eggs on my own. I ran
 scripts/scramble.py and this also failed with the following message (after
 building a lot of things):

 scramble(): Copied egg to:
   /nfs/users/galaxy_dist/eggs/twill-0.9-py2.7.egg
 Traceback (most recent call last):
   File scripts/scramble.py, line 26, in module
 eggs = c.scramble()
   File /nfs/users/galaxy_dist/lib/galaxy/eggs/scramble.py, line 242, in
 scramble
 raise last_exc # only 1 failure out of the crate, be more informative
 galaxy.eggs.scramble.ScrambleFailure: run_scramble_script(): Egg build
 failed for bx_python 0.7.1


 May I ask what may cause this problem? Have I done anything wrong? Or, is it
 even possible to install Galaxy on ARM architecture Linux?



 Many thanks,
 Shun


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Re: [galaxy-user] Error using Trackster

2013-02-01 Thread James Taylor
What is the type of the file from GEO? Any additional information you
provide will help debug this.

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Fri, Feb 1, 2013 at 1:53 PM, Kilaru, Varun vkil...@emory.edu wrote:
 Hi,
 Good day. I have been trying to use trackster on a file I downloaded from
 the NCBI GEO. However, it fails with the following error:

 hashMustFindVal: 'chr11' not found
 grep: writing output: Broken pipe

 This is followed by a number of lines of the same error code. I am not sure
 what is happening. Can you please elaborate?

 Thanks,
 Varun


 

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Re: [galaxy-user] [galaxy-dev] Workflows

2013-01-16 Thread James Taylor
Neil,

.../api/workflows is not a path in the galaxy directory, but a URL
that you should access over HTTP. For example, if you login to Galaxy
Test, and then access https://test.g2.bx.psu.edu/api/workflows you
will get a json dict of all of your workflows, including the workflow
id that you are looking for.


--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Tue, Jan 15, 2013 at 8:52 PM,  neil.burd...@csiro.au wrote:
 Hi

Sorry if these questions are obvious but I just don’t know how to find
 the answers.



 I’m trying to get one of the API examples to work in
 http://wiki.galaxyproject.org/Learn/API/Examples .



 I’ve got my API key but how do I get/find the workflow id (f2db41e1fa331b3e
 in the examples). I’ve created workflow but don’t know how to access this
 key.



 Also in the first example it states galaxy_url/api/workflows However I
 don’t have the “api/workflows” directory structure in my galaxy-dist, do I
 need to create this?



 Thanks

 Neil




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Re: [galaxy-user] galaxy test dataset listing

2013-01-04 Thread James Taylor
You are probably seeing the mtDNA re-sequencing datasets associated
with this paper:

  http://genomebiology.com/2011/12/6/R59

--
James Taylor, Assistant Professor, Biology/CS, Emory University


On Fri, Jan 4, 2013 at 10:46 AM, Sun, Wenping [USA] sun_wenp...@bah.com wrote:
 Hello,



 It is good to see there are some testing dataset in fastq format from galaxy
 s3. Is there any brief information about the test data? For example, RNAseq
 or Chipseq, etc?



 Many thanks,

 Kathryn


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Re: [galaxy-user] Galaxy CloudMan - Nodes can't make their own qsub calls?

2012-09-13 Thread James Taylor
You probably need to sudo to sgeadmin (cloudman guys correct me if you
have this setup differently).

I don't see any reason not to make worker nodes submit hosts by
default in a future cloudman release.

-- jt


On Thu, Sep 13, 2012 at 4:17 PM, greg margeem...@gmail.com wrote:
 As a follow up I found a command that should add the new nodes as
 submit hosts and I tried to run it but I got this error:

 $ qconf -as ip-10-28-164-178.ec2.internal
 denied: ubuntu must be manager for this operation

 What does it mean by manager?  How would I run this command?


 I guess my preference is for Cloudman to do this automatically though
 so I'll be distributing this program to 3rd party users using the
 built-in cloudman sharing.  I can't rightly ask users to be running
 qconf.

 Thanks again,

 Greg


 On Thu, Sep 13, 2012 at 3:59 PM, greg margeem...@gmail.com wrote:
 Hi guys,

 I created a new Galaxy instance web launcher
 (https://biocloudcentral.herokuapp.com/launch) and then I ssh'd into
 the master node.

 I'm trying to run a Perl script that makes several qsub calls to other
 perl scripts.  Now the catch is that one of those perl scripts makes
 its own qsub calls.

 And I'm getting this error when it tries to do that:

 Unable to run job: denied: host ip-10-29-176-111.ec2.internal is no
 submit host.


 Somehow this works fine on other clusters I've run this code on.  Any
 idea what could be going on?  Do I need to make all of the nodes
 submit hosts?

 Thanks a bunch!

 -Greg
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Re: [galaxy-user] [Genome] Problems with MAF blocks from Galaxy

2011-01-12 Thread James Taylor
Excerpts from ele.ga...@tiscali.it's message of Wed Jan 12 15:19:36 + 2011:

 I have a problem with MAF blocks using Galaxy. 

Hi Elena, I'm copying the galaxy-user list since this is a Galaxy
related question.

 1) the starting position of the MAF block extracted from Galaxy is
 shifted of one position downstream;

If you enter a region into the position box in the genome browser, it
will interpret it as one-based. However, when working with bed files in
Galaxy (and the genome browser) the intervals are zero-based. This is
likely the problem.

 2) the number of species displayed is not 28 in both Maf (from Galaxy)
 and Genome Browser.

This is entirely expected. If the alignment procedure does not identify
putatively orthologous sequence in the other species, no sequence will
be shown in the MAF output for that species. There are several reasons
this could happen, including: no significant pairwise local alignment
found by lastz, or a signifigant alignment found, but eliminated 
by the chaining/netting procedure.

 3) the alignment seems to be different (for example, species that have
 aligned sequences in the Genome Browser, are not in the MAF block
 retrieve from Galaxy).

Can you point out an example of this? In particular, are you sure you
are using the same original alignments in Galaxy and the Genome Browser?

Thanks,
James

-- 
James Taylor, Assistant Professor, Biology / Computer Science, Emory University
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