| BioPerl documentation | Contained in the BioPerl distribution. |
Bio::Tools::ERPIN - a parser for ERPIN output
use Bio::Tools::ERPIN;
my $parser = Bio::Tools::ERPIN->new( -file => $rna_output,
-motiftag => 'protein_bind'
-desctag => 'TRAP_binding');
#parse the results
while( my $motif = $parser->next_prediction) {
# do something here
}
Parses raw ERPIN output.
This module is not currently complete. As is, it will parse raw ERPIN long format output and pack information into Bio::SeqFeature::Generic objects.
Several values have also been added in the 'tag' hash. These can be accessed using the following syntax:
my ($entry) = $feature->get_Annotations('SecStructure');
Added tags are : tset - training set used for the sequence tsetdesc - training set description line cutoff - cutoff value used database - name of database dbdesc - description of database dbratios - nucleotide ratios of database (used to calculate evalue) descline - entire description line (in case the regex used for sequence ID doesn't adequately catch the name accession - accession number of sequence (if present) logodds - logodds score value sequence - sequence from hit, separated based on training set
See t/ERPIN.t for example usage.
At some point a more complicated feature object may be used to support this data rather than forcing most of the information into tag/value pairs in a SeqFeature::Generic. This will hopefully allow for more flexible analysis of data (specifically RNA secondary structural data).
User feedback is an integral part of the evolution of this and other Bioperl modules. Send your comments and suggestions preferably to the Bioperl mailing list. Your participation is much appreciated.
bioperl-l@bioperl.org - General discussion http://bioperl.org/wiki/Mailing_lists - About the mailing lists
Please direct usage questions or support issues to the mailing list:
bioperl-l@bioperl.org
rather than to the module maintainer directly. Many experienced and reponsive experts will be able look at the problem and quickly address it. Please include a thorough description of the problem with code and data examples if at all possible.
Report bugs to the Bioperl bug tracking system to help us keep track of the bugs and their resolution. Bug reports can be submitted via the web:
https://redmine.open-bio.org/projects/bioperl/
Email cjfields-at-uiuc-dot-edu
The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _
Title : new
Usage : my $obj = Bio::Tools::ERPIN->new();
Function: Builds a new Bio::Tools::ERPIN object
Returns : an instance of Bio::Tools::ERPIN
Args : -fh/-file for input filename
-motiftag => primary tag used in gene features (default 'misc_binding')
-desctag => tag used for display_name name (default 'erpin')
-srctag => source tag used in all features (default 'ERPIN')
Title : motiftag
Usage : $obj->motiftag($newval)
Function: Get/Set the value used for 'motif_tag', which is used for setting the
primary_tag.
Default is 'misc_binding' as set by the global $MotifTag.
'misc_binding' is used here because a conserved RNA motif is capable
of binding proteins (regulatory proteins), antisense RNA (siRNA),
small molecules (riboswitches), or nothing at all (tRNA,
terminators, etc.). It is recommended that this be changed to other
tags ('misc_RNA', 'protein_binding', 'tRNA', etc.) where appropriate.
For more information, see:
http://www.ncbi.nlm.nih.gov/collab/FT/index.html
Returns : value of motif_tag (a scalar)
Args : on set, new value (a scalar or undef, optional)
Title : source_tag
Usage : $obj->source_tag($newval)
Function: Get/Set the value used for the 'source_tag'.
Default is 'ERPIN' as set by the global $SrcTag
Returns : value of source_tag (a scalar)
Args : on set, new value (a scalar or undef, optional)
Title : desc_tag
Usage : $obj->desc_tag($newval)
Function: Get/Set the value used for the query motif. This will be placed in
the tag '-display_name'. Default is 'erpin' as set by the global
$DescTag. Use this to manually set the descriptor (motif searched for).
Since there is no way for this module to tell what the motif is from the
name of the descriptor file or the ERPIN output, this should
be set every time an ERPIN object is instantiated for clarity
Returns : value of exon_tag (a scalar)
Args : on set, new value (a scalar or undef, optional)
Usage : $obj->analysis_method();
Purpose : Inherited method. Overridden to ensure that the name matches
/ERPIN/i.
Returns : String
Argument : n/a
Title : next_feature
Usage : while($gene = $obj->next_feature()) {
# do something
}
Function: Returns the next gene structure prediction of the ERPIN result
file. Call this method repeatedly until FALSE is returned.
The returned object is actually a SeqFeatureI implementing object.
This method is required for classes implementing the
SeqAnalysisParserI interface, and is merely an alias for
next_prediction() at present.
Returns : A Bio::Tools::Prediction::Gene object.
Args : None (at present)
Title : next_prediction
Usage : while($gene = $obj->next_prediction()) {
# do something
}
Function: Returns the next gene structure prediction of the ERPIN result
file. Call this method repeatedly until FALSE is returned.
Returns : A Bio::Tools::Prediction::Gene object.
Args : None (at present)
| BioPerl documentation | Contained in the BioPerl distribution. |
# # BioPerl module for Bio::Tools::ERPIN # # Please direct questions and support issues to <bioperl-l@bioperl.org> # # Cared for by Chris Fields <cjfields-at-uiuc-dot-edu> # # Copyright Chris Fields # # You may distribute this module under the same terms as perl itself # POD documentation - main docs before the code
# Let the code begin... package Bio::Tools::ERPIN; use strict; use Bio::SeqFeature::Generic; use base qw(Bio::Tools::AnalysisResult); our($MotifTag,$SrcTag,$DescTag) = qw(misc_binding ERPIN erpin);
sub _initialize { my($self,@args) = @_; $self->warn('Use of this module is deprecated. Use Bio::SearchIO::erpin instead'); $self->SUPER::_initialize(@args); my ($motiftag,$desctag,$srctag) = $self->SUPER::_rearrange([qw(MOTIFTAG DESCTAG SRCTAG )], @args); $self->motif_tag(defined $motiftag ? $motiftag : $MotifTag); $self->source_tag(defined $srctag ? $srctag : $SrcTag); $self->desc_tag(defined $desctag ? $desctag : $DescTag); foreach (qw(_tset _tset_desc _cutoff _db _db_desc _db_ratios _eval_cutoff _seqid _secacc _seqdesc )) { $self->{$_}=''; } }
sub motif_tag{ my $self = shift; return $self->{'motif_tag'} = shift if @_; return $self->{'motif_tag'}; }
sub source_tag{ my $self = shift; return $self->{'source_tag'} = shift if @_; return $self->{'source_tag'}; }
sub desc_tag{ my $self = shift; return $self->{'desc_tag'} = shift if @_; return $self->{'desc_tag'}; }
#------------- sub analysis_method { #------------- my ($self, $method) = @_; if($method && ($method !~ /ERPIN/i)) { $self->throw("method $method not supported in " . ref($self)); } return $self->SUPER::analysis_method($method); }
sub next_feature { my ($self,@args) = @_; # even though next_prediction doesn't expect any args (and this method # does neither), we pass on args in order to be prepared if this changes # ever return $self->next_prediction(@args); }
sub next_prediction { my ($self) = @_; my ($motiftag,$srctag,$desctag) = ( $self->motif_tag, $self->source_tag, $self->desc_tag); # hit vars my ($strand, $start, $end, $sequence, $logodds, $score)=0; while($_ = $self->_readline) { #skip blank lines next if /^\s+$/; # parse header; there's probably a better way to do this, perhaps by # mapping, but this works for now... if(/^Training set:\s+\"(.*)\":$/) { $self->{'_tset'}=$1; } elsif(/\s+(\d+ sequences of length \d+)/){ $self->{'_tset_descr'}=$1; } elsif(/^Cutoff:\s+(\S+)\s+$/) { $self->{'_cutoff'}=$1; } elsif(/^Database:\s+\"(.*)\"$/) { $self->{'_db'}=$1; } elsif(/^\s+(\d+ nucleotides to be processed in \d+ sequence)$/) { $self->{'_db_desc'}=$1; } elsif(/^\s+ATGC ratios:\s(\d.\d+)\s+(\d.\d+)\s+(\d.\d+)\s+(\d.\d+)$/) { my $atgc=sprintf("A=%0.3f T=%0.3f G=%0.3f C=%0.3f", $1, $2, $3, $4); $self->{'_db_ratios'}=$atgc; } elsif(/^E-value at cutoff \S+ for \S+(?:G|M|k)?b double strand data: (\S+)/) { $self->{'_eval_cutoff'}=$1; } # catch hit, store in private hash keys elsif (/^>(.*)/) { $self->{_seq_desc} = $1; if($self->{_seq_desc} =~ /(?:P<db>gb|gi|emb|dbj|sp|pdb|bbs|ref|lcl)\|(\d+)((?:\:|\|)\w+\|(\S*.\d+)\|)?/) { $self->{_seqid} = $1; # pulls out gid $self->{_seq_acc} = $3; } else { $self->{_seqid} = $self->{_seq_desc}; $self->{_seq_acc} = ''; } } # parse next hit elsif (/^(FW|RC)\s+\d+\s+(\d+)..(\d+)\s+(\d+.\d+)\s+(.*)/) { ($strand, $start, $end, $logodds, $score)=($1, $2, $3, $4, $5); $score =~ s/^e/1e/i; chomp ($sequence = $self->_readline); # grab next line, which is the sequence hit my $gene = Bio::SeqFeature::Generic->new(-seq_id => $self->{_seqid}, -start => $start, -end => $end, -strand => $strand eq 'FW' ? 1 : -1, -score => $score, -primary_tag => $motiftag, -source_tag => $srctag, -display_name => $desctag, -tag => { 'tset' => $self->{_tset}, 'tsetdesc' => $self->{_tset_descr}, 'cutoff' => $self->{_cutoff}, 'database' => $self->{_db}, 'dbdesc' => $self->{_db_desc}, 'dbratios' => $self->{_db_ratios}, 'descline' => $self->{_seq_desc}, 'accession' => $self->{_seq_acc}, 'logodds' => $logodds, 'sequence' => $sequence} ); return $gene; } #else { # $self->debug("unrecognized line: $_"); #} } } 1;