[Bioperl-l] Re (3): Status of assembly modules
Lee Katz
lskatz at gmail.com
Fri Dec 10 23:53:38 UTC 2010
I am wondering if there is a way to optimize the BioPerl code for Assembly
IO. Specifically, when I convert a 2.2 MB genome (~200 contigs) from a 454
ace file to a regular ace file, it takes a few hours to get through 30
contigs using the code below (I estimate more than a day to get through all
of it).
Is there a way to optimize it? To convert a sequence file to another format
at most would take a minute and therefore converting an ace on the magnitude
of hours or days is too much. I wish I understood bioperl better but I
think the best I can do is issue a challenge or a feature request: who can
speed up Assembly::IO::ace?
# convert a Newbler ace to a standard ace
sub _newblerAceToAce($args){
my($self,$args)=@_;
my
$ace454=Bio::Assembly::IO->new(-file=>$$args{ace454Path},-format=>"ace",-variant=>'454');
my $ace=Bio::Assembly::IO->new(-file=>">$$args{acePath}",-format=>"ace");
#output ace
my $numContigs=`grep -c ^CO $$args{ace454Path}`+0;
logmsg "Converting $$args{ace454Path} (454-ace) to $$args{acePath} (ace).
$numContigs contigs total.";
while(my $contig=$ace454->next_contig){
logmsg "Finished with ".$contig->id ." out of $numContigs";
$ace->write_contig($contig);
}
return $$args{acePath};
}
Message: 3
Date: Mon, 22 Nov 2010 15:18:10 -0500
From: Lee Katz <lskatz at gatech.edu>
Subject: [Bioperl-l] Re(2): Status of assembly modules
To: bioperl-l at lists.open-bio.org
Message-ID:
<AANLkTi=JShCLsHDxHK4eeWD3Da=vWmRkGN2rkuLwCjxn at mail.gmail.com>
Content-Type: text/plain; charset=UTF-8
I figured it out (I haven't tested much though).
To whoever works on Assembly::IO::ace.pm:
I changed a regular expression on line 231 because the contig object was not
initializing properly. For some reason the 454 ace file had adopted the
reference assembly's ID and therefore there was a GI number followed by a
pipe. The pipe was not captured with \w+. I think that the regex will be
safe with \s(\S+)\s.
if (/^CO\s(\S+)\s(\d+)\s(\d+)\s(\d+)\s(\w+)/xms) { # New contig starts!
#if (/^CO\s(\w+)\s(\d+)\s(\d+)\s(\d+)\s(\w+)/xms) { # New contig starts!
On Thu, Nov 18, 2010 at 12:04 PM, <bioperl-l-request at lists.open-bio.org
>wrote:
> Message: 3
> Date: Wed, 17 Nov 2010 22:20:03 -0500
> From: Lee Katz <lskatz at gatech.edu>
> Subject: Re: [Bioperl-l] Status of assembly modules
> To: bioperl-l at lists.open-bio.org
> Message-ID:
> <AANLkTi=aFAnYrEXj3D4joZeYwxRT971M_ZYR0uFJOrxc at mail.gmail.com>
> Content-Type: text/plain; charset=UTF-8
>
> I have read on the BioPerl site that a 454 ace is not standardized due to
> its coordinate system. How can I convert it to the standard ace file?
>
> When I run this code either by using contig or assembly objects, I get an
> error.
> Can't call method "get_consensus_sequence" on an undefined value at
> Bio/Assembly/IO/ace.pm line 280, <GEN0> line 93349.
>
> sub _newblerAceToAce($args){
> my($self,$args)=@_;
> my
>
> $ace454=Bio::Assembly::IO->new(-file=>$args{ace454Path},-format=>"ace
",-variant=>'454');
> my
> $ace=Bio::Assembly::IO->new(-file=>">$args{acePath}",-format=>"ace");
> #while(my $contig=$ace454->next_contig){
> while(my $scaffold=$ace454->next_assembly){
> print Dumper $scaffold;
> }
> return $args{acePath};
> }
>
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