[Gmod-help] Re: [maker-devel] [Gmod-gbrowse] Best practices for generating alignments for GBrowse...
Bob Freeman
bob_freeman at hms.harvard.edu
Mon Aug 17 12:50:47 EDT 2009
Thanks, all, for the *extremely* helpful suggestions. This will save
me greatly in personal and compute time!!
I am poised to run MAKER to generate additional gene models to
complement those generated from Baylor -- I may contact Carson and
Mark separately with some very specific questions.
Best,
Bob
On Aug 14, 2009, at 6:03 PM, Carson Holt wrote:
>
> >>My basic outline for mapping related genes is to use BLAST for
> >>a coarse location, then exonerate for a refined mapping.
> >>Using just exonerate w/o pre-located genes is possible but
> >>you end up with a much large compute task and generally
> >>more gene mappings than you know what to do with.
>
> MAKER runs both blast and exonerate internally so it takes care of
> this for you.
>
>
> >>The short answer is
> >>if the assemblies don't change much then tools will
> >>move annotations from one to the next. If they do
> >>change, you are generally better off re-running your
> >>gene-finding, gene-mapping software.
>
> MAKER can do this too. MAKER can run gene-finders like snap,
> genemark, augustus, fgenesh for you. In addition, MAKER also
> produces evidence informed “hints” based on the EST and protein
> alignments as well as mRNAs from closely related species. MAKER
> then talks to the gene predictors using the hints and causes them to
> produce even better gene models. MAKER will also revise these gene
> models to include five and three prime UTRs when there is support
> from EST evidence.
>
> MAKER will also run other programs for you like RepeatMasker if you
> choose. There are also tools for running InterProScan (a protein
> domain finder), as well as tools for automatically assigning GO
> functional terms and putative gene functions to each new gene
> prediction.
>
> The newest revision of MAKER also comes with a handy maker2chado
> script that will auto-load all MAKER produced GFF3 files into a new
> or pre-existing chado database for you.
>
> Carson
>
>
>
> On 8/14/09 3:31 PM, "Don Gilbert" <gilbertd at cricket.bio.indiana.edu>
> wrote:
>
>
>
>
> Bob,
>
> Here is my two-bits advice on your general questions of gene to genome
> mapping tools.
>
> >> Specifically, we'd like to load the following:
> >> ESTs positioned against genomic scaffolds (same species)
> >> BLAST? or a better program?
>
> GMAP is the one I use and recommend for EST alignments,
> but BLAT works, exonerate, BLAST and others also work.
>
> >> Full-length mRNAs/clones (same species)
> >> BLAST? or something better?
>
> add exonerate here (maybe the older GeneWise). exonerate will give
> you more complete gene/mRNA mappings than BLAST.
>
> >> mRNAs from closely-related organisms for cross-species
> comparisons on gene
> >> structure
> add exonerate here
>
> >> ?
> >> proteins from closely-related organisms for cross-species
> comparisons on
> >> gene structure
> exonerate
>
> My basic outline for mapping related genes is to use BLAST for
> a coarse location, then exonerate for a refined mapping.
> Using just exonerate w/o pre-located genes is possible but
> you end up with a much large compute task and generally
> more gene mappings than you know what to do with.
>
> For your question of remapping to new assemblies, if the
> MAKER or Flybase answers are not what you want, look at
> UCSC genomes, and Jim Kent's software. They do a lot
> of that, mapping b/n assemblies. The short answer is
> if the assemblies don't change much then tools will
> move annotations from one to the next. If they do
> change, you are generally better off re-running your
> gene-finding, gene-mapping software.
>
> -- Don
>
> -- d.gilbert--bioinformatics--indiana-u--bloomington-in-47405
> -- gilbertd at indiana.edu--http://marmot.bio.indiana.edu/
>
> _______________________________________________
> maker-devel mailing list
> maker-devel at yandell-lab.org
> http://yandell-lab.org/mailman/listinfo/maker-devel_yandell-lab.org
>
>
-----------------------------------------------------
Bob Freeman, Ph.D.
Acorn Worm Informatics, Kirschner lab
Dept of Systems Biology, Alpert 524
Harvard Medical School
200 Longwood Avenue
Boston, MA 02115
617/432.2293, vox
When choosing between two evils I always take the one I've never tried
before. -- Mae West, Klondike Annie
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