Gowtham,
Maybe slightly off topic but it finally comes into Artemis or ACT :-)
We actually do not use abacas. We use several types of contig 
ordering/scafolding (depending on whether there is a reference and whether or 
not we have PE libraries).
Mostly I layout contigs using BLAT to a reference (if we have one) and use the 
result to make a contig order/orientation list which is then joined by a perl 
script in correct order giving the option to insert recognisable/functional 
linkers between them. At that stage we also write out the FT file which can be 
loaded as a track. Example is below;
The advantage of doing it like this was that we could extend these scripts with 
getting the coverage from the assembly files and pulling them as custom plots 
into Artemis as well.
Alex

example FT:

FT   misc_feature    1..53
FT                   /label="Joiner"
FT                   /colour=255 99 71
FT   exon            54..22598
FT                   /label="700917_contig00117"
FT                   /colour=152 251 152
FT   misc_feature    22599..22651
FT                   /label="Joiner"
FT                   /colour=255 99 71
FT   exon            22652..23638
FT                   /label="700917_contig00089"
FT                   /colour=152 251 152
FT   misc_feature    23639..23691
FT                   /label="Joiner"
FT                   /colour=255 99 71
FT   exon            23692..29133
FT                   /label="RevCompl_700917_contig00127"
FT                   /colour=135 206 250
FT   misc_feature    29134..29186

=========== snip ==========


________________________________________
Van: Gowthaman Ramasamy [gowthaman.ramas...@seattlebiomed.org]
Verzonden: donderdag 15 december 2011 15:50
Aan: Bossers, Alex; Julian Parkhill; Gowthaman Ramasamy
CC: artemis-users@sanger.ac.uk
Onderwerp: Re: [Artemis-users] Customizing crunch file in ACT...

That's a wonderful idea.  In fact I already load the contig's FT track (from 
Abacas's). But, it never occurred to me that we can modify it to load linker 
information as well. After Alex's email,
I am started to wonder if the linkers are providing any value addition at all?. 
 I will have to explore.....

Thanks very much Alex.
Gowtham

PS: Are you using Abacas by any chance Alex? If so, can I ask couple questions 
offline. Thanks.


On 12/14/11 11:26 PM, "Bossers, Alex" <alex.boss...@wur.nl> wrote:

Alternatively (as we do it) we generate an EMBL FT track containing the layout 
of contigs (incl any rev complementing and/or linkers). Works quite well for us 
and keeps comparison files clean/original.
ALex

-----Oorspronkelijk bericht-----
Van: artemis-users-boun...@sanger.ac.uk 
[mailto:artemis-users-boun...@sanger.ac.uk] Namens Julian Parkhill
Verzonden: woensdag 14 december 2011 9:42
Aan: Gowthaman Ramasamy
CC: artemis-users@sanger.ac.uk
Onderwerp: Re: [Artemis-users] Customizing crunch file in ACT...

Gowthaman ,

The right hand scroll bar controls the display of links based on size of the 
hit (removing shorter hits up to 1kb). If you want to control the display based 
on the score, then right click in the centre window and select "Set Score 
Cutoffs ..."

Julian.

On 13 Dec 2011, at 23:20, Gowthaman Ramasamy wrote:

> Hi Everyone,
> I trying to trick ACT to display linking bars from two different blast out 
> files.
>
> I have a chromosome at one side and newly scaffolded  chromosome on the other 
> side  (generated by ordering of contigs using Abacas). I want to display two 
> kinds of link between them.
>
> 1.  crunch file from Abacas. To show matching/ordered contigs. So there will 
> be only few super wide bars.
> 2.  tblastx outfile between these chromosomes (used MSPcrunch to match with 
> Abacas outfile output)
>
> I manually fuse both the files and use in ACT. It display links from both. 
> But, I want to make abacas crunch disappear most of the time.
> My naïve attempt was to change score in the Abacas crunch file to"zero" 
> artificially, so that I can block that link using the ACT 's middle window 
> scroll bar. But, it does not respond. I mean, it does not control the display 
> based on score.
>
> But, when I load un modified blastout file (with  -m 9) option, it seems to 
> control the display. Is it something a known issue.
>
> Better, yet, is there any better way to use two different crunch/blast out 
> files?
> Gowthaman
>
> PS: I can load one chromosome twice. But, anything else?
>
> _______________________________________________
> Artemis-users mailing list
> Artemis-users@sanger.ac.uk
> http://lists.sanger.ac.uk/mailman/listinfo/artemis-users

Julian Parkhill
Tel: +44(0)1223 494902






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