# $Id: EPCR.pm 16123 2009-09-17 12:57:27Z cjfields $ # # BioPerl module for Bio::Tools::EPCR # # Please direct questions and support issues to # # Cared for by Jason Stajich # # Copyright Jason Stajich # # You may distribute this module under the same terms as perl itself # POD documentation - main docs before the code =head1 NAME Bio::Tools::EPCR - Parse ePCR output and make features =head1 SYNOPSIS # A simple annotation pipeline wrapper for ePCR data # assuming ePCR data is already generated in file seq1.epcr # and sequence data is in fasta format in file called seq1.fa use Bio::Tools::EPCR; use Bio::SeqIO; my $parser = Bio::Tools::EPCR->new(-file => 'seq1.epcr'); my $seqio = Bio::SeqIO->new(-format => 'fasta', -file => 'seq1.fa'); my $seq = $seqio->next_seq || die("cannot get a seq object from SeqIO"); while( my $feat = $parser->next_feature ) { # add EPCR annotation to a sequence $seq->add_SeqFeature($feat); } my $seqout = Bio::SeqIO->new(-format => 'embl'); $seqout->write_seq($seq); =head1 DESCRIPTION This object serves as a parser for ePCR data, creating a Bio::SeqFeatureI for each ePCR hit. These can be processed or added as annotation to an existing Bio::SeqI object for the purposes of automated annotation. =head1 FEEDBACK =head2 Mailing Lists 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 =head2 Support Please direct usage questions or support issues to the mailing list: I 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. =head2 Reporting Bugs 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: http://bugzilla.open-bio.org/ =head1 AUTHOR - Jason Stajich Email jason-at-bioperl.org =head1 APPENDIX The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _ =cut # Let the code begin... package Bio::Tools::EPCR; use strict; use Bio::SeqFeature::FeaturePair; use Bio::SeqFeature::Generic; use base qw(Bio::Root::Root Bio::SeqAnalysisParserI Bio::Root::IO); =head2 new Title : new Usage : my $epcr = Bio::Tools::EPCR->new(-file => $file, -primary => $fprimary, -source => $fsource, -groupclass => $fgroupclass); Function: Initializes a new EPCR parser Returns : Bio::Tools::EPCR Args : -fh => filehandle OR -file => filename -primary => a string to be used as the common value for each features '-primary' tag. Defaults to 'sts'. (This in turn maps to the GFF 'type' tag (aka 'method')). -source => a string to be used as the common value for each features '-source' tag. Defaults to 'e-PCR'. (This in turn maps to the GFF 'source' tag) -groupclass => a string to be used as the name of the tag which will hold the sts marker namefirst attribute. Defaults to 'name'. =cut sub new { my($class,@args) = @_; my $self = $class->SUPER::new(@args); my ($primary, $source, $groupclass) = $self->_rearrange([qw(PRIMARY SOURCE GROUPCLASS)],@args); $self->primary(defined $primary ? $primary : 'sts'); $self->source(defined $source ? $source : 'e-PCR'); $self->groupclass(defined $groupclass ? $groupclass : 'name'); $self->_initialize_io(@args); return $self; } =head2 next_feature Title : next_feature Usage : $seqfeature = $obj->next_feature(); Function: Returns the next feature available in the analysis result, or undef if there are no more features. Example : Returns : A Bio::SeqFeatureI implementing object, or undef if there are no more features. Args : none =cut sub next_feature { my ($self) = @_; my $line = $self->_readline; return unless defined($line); chomp($line); my($seqname,$location,$mkrname, $rest) = split(/\s+/,$line,4); my ($start,$end) = ($location =~ /(\S+)\.\.(\S+)/); # `e-PCR -direct` results code match strand in $rest as (+) and (-). Decode it if present. my $strandsign; if ($rest =~ m/^\(([+-])\)(.*)$/) { ($strandsign,$rest) = ($1, $2); } else { $strandsign = "?"; } my $strand = $strandsign eq "+" ? 1 : $strandsign eq "-" ? -1 : 0; my $markerfeature = Bio::SeqFeature::Generic->new ( '-start' => $start, '-end' => $end, '-strand' => $strand, '-source' => $self->source, '-primary' => $self->primary, '-seq_id' => $seqname, '-tag' => { $self->groupclass => $mkrname, ($rest ? ('Note' => $rest ) : ()), }); #$markerfeature->add_tag_value('Note', $rest) if defined $rest; return $markerfeature; } =head2 source Title : source Usage : $obj->source($newval) Function: Example : Returns : value of source (a scalar) Args : on set, new value (a scalar or undef, optional) =cut sub source{ my $self = shift; return $self->{'_source'} = shift if @_; return $self->{'_source'}; } =head2 primary Title : primary Usage : $obj->primary($newval) Function: Example : Returns : value of primary (a scalar) Args : on set, new value (a scalar or undef, optional) =cut sub primary{ my $self = shift; return $self->{'_primary'} = shift if @_; return $self->{'_primary'}; } =head2 groupclass Title : groupclass Usage : $obj->groupclass($newval) Function: Example : Returns : value of groupclass (a scalar) Args : on set, new value (a scalar or undef, optional) =cut sub groupclass{ my $self = shift; return $self->{'_groupclass'} = shift if @_; return $self->{'_groupclass'}; } 1;