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From: Scott C. <sc...@sc...> - 2012-10-18 15:32:30
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Hi xukai, What do you have now? Just the fasta sequences of the contigs? If so, all you need to do is create one GFF line for each contig, which would look something like this: contig1234 . contig 1 <length> . . . Name=contig1234 You can also put the sequence of the contig at the bottom of the GFF file if you like: ...gff lines... ##FASTA >contig1234 atgaatagc.... This is fairly easy to do with a short perl script. If you don't want to write one yourself, there is a script called gmod_fasta2gff3.pl in the Chado distribution: http://gmod.svn.sourceforge.net/viewvc/gmod/schema/trunk/chado/bin/gmod_fasta2gff3.pl?revision=25275&content-type=text%2Fplain It only relies on BioPerl, so you can download it directly without getting all of Chado. Scott On Thu, Oct 18, 2012 at 5:05 AM, Kai Xu <xuk...@gm...> wrote: > hey guys, > > i am learning how to use the GBrowse_syn to do a comparison between two > bacillus strains. one of them is complete sequence but the other is a draft > sequence which contains many contigs. now i have finished the BLAST between > the two strains and converted the BLAST results to clustalW format. but when > i import the sequence into GBrowse_syn, as we know that it requires the > sequence to be GFF3 format. so how can i deal with the draft sequence? can > anyone give me some suggestions? thanks. > > yours, > xukai > > ------------------------------------------------------------------------------ > Everyone hates slow websites. So do we. > Make your web apps faster with AppDynamics > Download AppDynamics Lite for free today: > http://p.sf.net/sfu/appdyn_sfd2d_oct > _______________________________________________ > Gmod-gbrowse mailing list > Gmo...@li... > https://lists.sourceforge.net/lists/listinfo/gmod-gbrowse > -- ------------------------------------------------------------------------ Scott Cain, Ph. D. scott at scottcain dot net GMOD Coordinator (http://gmod.org/) 216-392-3087 Ontario Institute for Cancer Research |