Thanks James!

   Actually, these annotations I'm working with I've generated with your
dawgpaws pipeline :)
The thing is, I was hoping to be able to curate them which is why I was
wanting to use Apollo and gff3. Any idea on how I can work around this would
be great!

Cheers,

Elizabeth

On Wed, May 12, 2010 at 7:44 PM, James Estill <[email protected]>wrote:

> I think that if you do this is GFF2 format, it will work. All features will
> need to have the same id (ie. LTR_model_01).
>
> If you have Gbrowse installed, you can display full annotations of LTR
> retrotransposons using a glyph I wrote . Example images of the glyph are at
> http://sourceforge.net/apps/trac/dawgpaws/attachment/ticket/35/cartoon_zoomed_out.pngand
> http://sourceforge.net/apps/trac/dawgpaws/attachment/ticket/35/cartoon_zoomed_in.png
> .
>
> The source for the gbrowse glyph is at
> http://dawgpaws.svn.sourceforge.net/viewvc/dawgpaws/trunk/gbrowse/glyph/ltr_simple.pm?revision=960
>
> Unfortunately you can not curate annotations in Gbrowse, but it does allow
> you to see the biology of the TE.
>
> -- Jamie Estill
> -- [email protected]
> -- http://jestill.myweb.uga.edu
> -- http://www.epernicus.com/people/jestill
>
>
> ----- Original Message -----
> From: elizabeth henaff
> [mailto:[email protected]]
> To: [email protected]
> Sent: Wed, 12 May 2010
> 13:13:39 -0400
> Subject: Re: [apollo] parent - child tags for elements in
> gff3 that are not       genes
>
>
> > Hi Ed,
> >
> > Thanks for your response.
> >
> > The data I have is such that I had one Parent (retrotransposon) with
> > multiple children features (LTR, primer binding site, etc). It is
> meaningful
> > for me to retain these children features, so I was wondering of it would
> be
> > possible to circumvent the child-parent relationship by eliminating the
> > Parent feature, and representing all its children as one discontinuous
> > feature.
> > I've tried to do that by adding an identical ID attribute to the children
> > that belong together and "groupby : GENE" to the [type] definition but
> when
> > I load the gff3 I only see the first feature with a given ID.
> >
> > this is what I have added to gff3.tiers:
> >
> > [Tier]
> > tiername : LTR_de_novo
> > expanded : true
> > labeled : true
> > curated : true
> >
> > [Type]
> > label : LTR_retrotransposon
> > tiername : LTR_de_novo
> > datatype : primer_binding_site
> > datatype : RR_tract
> > datatype : five_prime_LTR
> > datatype : three_prime_LTR
> > datatype : target_site_duplication
> > datatype : transposon_fragment
> > glyph : ThinRectangle
> > color : red
> > utr_color : 250,250,210
> > column : GENOMIC_LENGTH 1
> > column : GENOMIC_RANGE 1
> > column : SCORE
> > column : NAME
> > column : Source
> > column : Strand
> >
> > and here's a snippet of the gff3 file:
> >
> > ##gff-version 3
> > MRGH6_contig ltr_finder:def three_prime_LTR 62941 64198 6 - .
> > Name=three_prime_LTR;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_1
> > MRGH6_contig ltr_finder:def primer_binding_site 62841 62857 6 - .
> > Name=primer_binding_site;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_1
> > MRGH6_contig ltr_finder:def RR_tract 56801 56815 6 - . Name=RR_tract;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_1
> > MRGH6_contig ltr_finder:def five_prime_LTR 55509 56766 6 - .
> > Name=five_prime_LTR;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_1
> > MRGH6_contig ltr_finder:def primer_binding_site 105081 105103 6 - .
> > Name=primer_binding_site;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_2
> > MRGH6_contig ltr_finder:def RR_tract 95013 95027 6 - . Name=RR_tract;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_2
> > MRGH6_contig ltr_finder:def five_prime_LTR 94168 95008 6 - .
> > Name=five_prime_LTR;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_2
> > MRGH6_contig ltr_finder:def three_prime_LTR 105170 106020 6 - .
> > Name=three_prime_LTR;
> > Source=ltr_finder:def; Strand=-; ID=ltr_finder:def_ltr_finder_2
> >
> >
> > Thanks for your help!
> >
> >
> >
> > Elizabeth
> >
> > On Wed, May 12, 2010 at 6:15 PM, Ed Lee <[email protected]> wrote:
> >
> > > Hi Elizabeth,
> > >
> > > The only parent-child relationships that Apollo currently supports
> > > is the gene-transcript-exon relationship.  Unless you need to retain
> > > the LTR relationship, I would suggest choosing the feature that
> > > reflects the analysis best (either the parent or child) and then
> > > removing the other (if removing the child, remember to remove the
> > > "Parent" attribute in the GFF3 file).
> > >
> > > Cheers,
> > > Ed
> > >
> > >
> > > On Wed, 12 May 2010, elizabeth henaff wrote:
> > >
> > >  Hello all,
> > >>
> > >> I'm trying to use Apollo to annotate transposable elements in some BAC
> > >> sequences. I have run various prediction programs that generate data
> in
> > >> GFF3
> > >> format, and my idea is to load these results into Apollo to be able to
> > >> manually curate them.
> > >>
> > >>
> > >> The nature of the data is such that there are Parent-Child
> relationships
> > >> between features (as defined by the Parent=xxx tag in the 9th column),
> > for
> > >> example a three_prime_LTR feature would have as a Parent a
> > >> LTR_retrotransposon feature, indicating that that LTR sequence belongs
> to
> > >> a
> > >> particular retrotransposon.
> > >>  When I load the gff3 file into Apollo, I get the following error
> > message:
> > >> "only transcripts and exons can be children of annotations:
> > >> three_prime_LTR[three_prime_LTR]"
> > >> and a similar error message for each feature that has a Parent tag.
> > >> Apollo then starts up, but only the features that do not have a Parent
> > tag
> > >> appear.
> > >>
> > >> In gff3.tiers I have defined a new [tier] as TE_annotation and a
> [type]
> > >> for
> > >> each of the datatypes (the second column of the gff3 file) present in
> my
> > >> gff3 file. For each of the [type] fields I defined the
> number_of_levels
> > >> field as 3, but that doesn't seem to fix the problem.
> > >> Any idea how I can resolve this?
> > >>
> > >> Thanks so much for any help!
> > >>
> > >> I've tried to attach the gff3, fasta and gff3.tiers files I'm using
> but
> > it
> > >> seems like it makes the message too big, but I'd be happy to send them
> if
> > >> that would help.
> > >> I'm running version 1.11.2 on ubuntu.
> > >>
> > >> Cheers,
> > >>
> > >> Elizabeth
> > >>
> > >> Centre de Recerca en AgriGenomica
> > >> Barcelona, Espanya
> > >>
> > >>
> >
>
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