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=head1 GBROWSE FAQ
Frequently asked questions - with answers.
=head1 GENERAL
=over 4
=item How do I get the most recent version of this FAQ?
The most recent version of this FAQ can be downloaded at
L<http://www.gmod.org/ggb/FAQ.html> and
L<http://www.gmod.org/ggb/FAQ.pod>.
=item What is GBrowse good for?
GBrowse was designed to view genomes. It displays a graphical
representation of a section of a genome, and shows the positions of
genes and other functional elements. It can be configured to show both
qualitative data such as the splicing structure of a gene, and
quantitative data such as microarray expression levels.
Another good way to get an overview of the features GBrowse offers is
to read the online tutorial at
L<http://www.gmod.org/ggb/tutorial/tutorial.html>.
=item What platforms does GBrowse run on?
GBrowse is a web-server application that is implemented in the Perl
programming language. It will run on any machine that runs Perl,
including Windows, Macintosh OS X, and most versions of Linux and
UNIX.
=item How is GBrowse distributed?
GBrowse is distributed as source code for Macintosh OS X, UNIX and
Linux platforms, and as pre-packaged binaries for Windows machines.
=item What are the terms of use for GBrowse?
GBrowse is distributed under the Perl Artistic License, which allows
for unrestricted use and distribution, including commercial use and
resale. You may modify and distribute modified versions of GBrowse
provided that you credit the original authors for their contribution.
=item I have a problem. What do I do?
First consult the mailing lists at
L<http://sourceforge.net/mailarchive/forum.php?forum_id=31947>. Your
problem may already have been reported and discussed. If you find no
help there, then send email to
E<gmod-gbrowse@lists.sourceforge.net>. If you are pretty
certain you have found a bug, please report it to the bug report
tracking system at
L<http://sourceforge.net/tracker/?func=add&group_id=27707&atid=511474>.
=back
=head1 INSTALLATION
=over 4
=item Where do I download GBrowse?
From
L<http://sourceforge.net/project/showfiles.php?group_id=27707>. If you
want to live on the bleeding edge, you may try the development version
of GBrowse. Instructions for accessing the development version of
GBrowse can be found at L<http://www.gmod.org/cvs.shtml>.
=item How do I install GBrowse?
After you unpack GBrowse, detailed installation instructions will be
found in the top level directory, in the file INSTALL. An online
version of this document can be found at
L<http://www.gmod.org/ggb/install.txt>.
=back
=head1 CONFIGURATION
=over 4
=item When I search, why doesn't GBrowse find my 3-letter gene name?
If you are using the MySQL GFF adaptor and are storing gene names
inside Note attributes, then you may bump up against MySQL's default
four-letter limit on full text searches. To fix this, either:
1. Put the gene name in an Alias attribute, e.g. "Alias LEP"
or
2. Change MySQL to allow searches on 3-character words.
The latter solution is a multi-step process:
1. Open /etc/my.cnf and add the following configuration line
to the [mysqld] stanza:
ft_min_word_len=3
2. Restart the mysql server.
3. Connect to your database using the mysql command-line client
and run the command:
mysql> repair table fattribute_to_feature quick;
=item How do I use semantic zooming to hide a track completely?
If you wish to turn off a track entirely, you can use the "hide" flag
to hide the track when the display exceeds a certain size:
[6_frame_translation:50000]
hide = 1
=item I have a multi-segmented feature (such as a multi-exon transcript). It looks fine at low power, but when I zoom in the connecting lines between segments disappear. Help!
You need to structure the feature in such a way that it has a single
parent part that spans the whole feature from end to end, and then use
the appropriate aggregator. For example, the "match" aggregator looks
for a parent feature of type "match" and subpart features of type
"HSP." So the GFF file you load should look like this:
Chr1 . match 1 1000 . . . ID=Hit27
Chr1 . HSP 1 200 . . . Parent=Hit27
Chr1 . HSP 500 600 . . . Parent=Hit27
Chr1 . HSP 900 1000 . . . Parent=Hit27
In GFF2 format, the example will look like this:
Chr1 . match 1 1000 . . . Hit Hit27
Chr1 . HSP 1 200 . . . Hit Hit27
Chr1 . HSP 500 600 . . . Hit Hit27
Chr1 . HSP 900 1000 . . . Hit Hit27
For transcripts, use the "processed_transcript" aggregator and create
features with a main part of "mRNA" and subparts of "CDS", "exon",
and/or various types of UTRs.
=item I'm using the GFF database adaptor. Is it better to load it using GFF2 or GFF3?
GFF2, described in the GBrowse tutorial, is the older version of the
GFF feature annotation format. Its main limitation is that it cannot
represent features that have more than one level of nested
subparts. For example, you cannot represent the relationship between a
gene, two alternatively spliced transcripts, and the exons inside the
transcripts. GFF3 (L<http://song.sourceforge.net>) corrects this
problem as well as a number of other deficiencies.
You can load a BioPerl GFF database using either GFF2 or GFF3
format. However, the BioPerl GFF database schema has not yet been
updated to handle the new features of GFF3. Therefore you will not
benefit from most of GFF3's features. In particular, BioPerl will use
the GFF3 ID as the name of the feature, rather than NAME (the provided
name will be recognizeed as a synonym). In addition, BioPerl allows
only one level of feature nesting.
The bottom line is that you might want to use GFF3 in order to have
forward-compatiility with new versions of Bio::DB::GFF. Otherwise GFF2
will work perfectly well.
=item How do I pass parameters into functions of init_code?
You want to define a function in the init_code section which will then
be called within callbacks.
The answer is to do something like this:
[GENERAL]
init_code = sub round {
my $a = shift;
return int($a + 0.5);
}
[TRACKS]
label = sub {
my $feature = shift;
my $score = $feature->score;
return "score = ",round($score);
}
Note that you'll need GBrowse version 1.63 or higher for this to work.
=item How do I show circular genomes?
GBrowse was designed for linear genomes. In order to represent
circular genomes, you'll need to break the circle open at a convenient
spot (preferably a spot that is not spanned by any genes). If you do
need to break a gene, you'll have to put two entries for it in the GFF
load file:
-----------------------------------------------------------
====> >==========
second half first half
You may have to give the two halves different names in order to
prevent GBrowse from trying to join the two halves. This is nonoptimal
and will be fixed in a later release.
=back
=head1 OTHER
=over
=item Why are there so few questions in the FAQ?
Because I just started this document.
=back
$Id: FAQ.pod,v 1.2 2005-12-09 22:19:09 mwz444 Exp $
|
