[Bioperl-l] using Bio::DB::GFF for aggregation
Aaron Mackey
ajmackey at gmail.com
Wed Jan 20 12:59:38 UTC 2010
I would advise using BEDtools or the R IRanges package for this kind of
aggregation/merging work, rather than trying to reinvent this particular
wheel.
-Aaron
On Wed, Jan 20, 2010 at 12:32 AM, Dan Kortschak <
dan.kortschak at adelaide.edu.au> wrote:
> Hi Chris (or others),
>
> I've been looking at ways to do large assemblies (really rnaseq/readseq
> comparisons for coverage) with maq/bowtie output and it's clear that for
> the size of project that I'm working on the space complexity is too
> nasty with Bio::DB::Sam. So I thought Bio::DB:GFF might be the way to
> go.
>
> I was thinking: B:T:R:Bowtie ~> B:SeqFeat:Generic -> B:T:GFF -> B:DB:GFF
>
> This depends on the behaviour of B:DB:GFF->features(-merge=>1). I've
> read through the docs, and it's not entirely clear (I'm hoping I've
> interpreted it the right way), but does this result in the return of
> features such that overlapping features are returned as a single feature
> while non-overlapping features come back separately. If this is the
> case, it would satisfy my requirements perfectly.
>
> thanks for your time
> Dan
>
> _______________________________________________
> Bioperl-l mailing list
> Bioperl-l at lists.open-bio.org
> http://lists.open-bio.org/mailman/listinfo/bioperl-l
>
More information about the Bioperl-l
mailing list