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# BioPerl module for Bio::Tools::EPCR |
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# Please direct questions and support issues to |
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# |
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# Cared for by Jason Stajich |
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# |
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# Copyright Jason Stajich |
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# |
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# You may distribute this module under the same terms as perl itself |
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# POD documentation - main docs before the code |
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=head1 NAME |
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Bio::Tools::EPCR - Parse ePCR output and make features |
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=head1 SYNOPSIS |
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# A simple annotation pipeline wrapper for ePCR data |
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# assuming ePCR data is already generated in file seq1.epcr |
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# and sequence data is in fasta format in file called seq1.fa |
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use Bio::Tools::EPCR; |
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use Bio::SeqIO; |
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my $parser = Bio::Tools::EPCR->new(-file => 'seq1.epcr'); |
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my $seqio = Bio::SeqIO->new(-format => 'fasta', -file => 'seq1.fa'); |
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my $seq = $seqio->next_seq || die("cannot get a seq object from SeqIO"); |
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while( my $feat = $parser->next_feature ) { |
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# add EPCR annotation to a sequence |
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$seq->add_SeqFeature($feat); |
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} |
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my $seqout = Bio::SeqIO->new(-format => 'embl'); |
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$seqout->write_seq($seq); |
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=head1 DESCRIPTION |
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This object serves as a parser for ePCR data, creating a |
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Bio::SeqFeatureI for each ePCR hit. These can be processed or added |
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as annotation to an existing Bio::SeqI object for the purposes of |
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automated annotation. |
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=head1 FEEDBACK |
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=head2 Mailing Lists |
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User feedback is an integral part of the evolution of this and other |
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Bioperl modules. Send your comments and suggestions preferably to |
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the Bioperl mailing list. Your participation is much appreciated. |
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bioperl-l@bioperl.org - General discussion |
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http://bioperl.org/wiki/Mailing_lists - About the mailing lists |
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=head2 Support |
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Please direct usage questions or support issues to the mailing list: |
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I |
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rather than to the module maintainer directly. Many experienced and |
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reponsive experts will be able look at the problem and quickly |
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address it. Please include a thorough description of the problem |
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with code and data examples if at all possible. |
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=head2 Reporting Bugs |
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Report bugs to the Bioperl bug tracking system to help us keep track |
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of the bugs and their resolution. Bug reports can be submitted via the |
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web: |
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https://github.com/bioperl/bioperl-live/issues |
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=head1 AUTHOR - Jason Stajich |
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Email jason-at-bioperl.org |
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=head1 APPENDIX |
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The rest of the documentation details each of the object methods. |
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Internal methods are usually preceded with a _ |
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=cut |
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# Let the code begin... |
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package Bio::Tools::EPCR; |
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use strict; |
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use Bio::SeqFeature::FeaturePair; |
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use Bio::SeqFeature::Generic; |
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use base qw(Bio::Root::Root Bio::SeqAnalysisParserI Bio::Root::IO); |
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=head2 new |
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Title : new |
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Usage : my $epcr = Bio::Tools::EPCR->new(-file => $file, |
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-primary => $fprimary, |
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-source => $fsource, |
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-groupclass => $fgroupclass); |
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Function: Initializes a new EPCR parser |
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Returns : Bio::Tools::EPCR |
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Args : -fh => filehandle |
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OR |
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-file => filename |
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-primary => a string to be used as the common value for |
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each features '-primary' tag. Defaults to |
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'sts'. (This in turn maps to the GFF 'type' |
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tag (aka 'method')). |
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-source => a string to be used as the common value for |
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each features '-source' tag. Defaults to |
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'e-PCR'. (This in turn maps to the GFF 'source' |
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tag) |
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-groupclass => a string to be used as the name of the tag |
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which will hold the sts marker namefirst |
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attribute. Defaults to 'name'. |
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=cut |
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sub new { |
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my($class,@args) = @_; |
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my $self = $class->SUPER::new(@args); |
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my ($primary, $source, |
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$groupclass) = $self->_rearrange([qw(PRIMARY |
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SOURCE |
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GROUPCLASS)],@args); |
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$self->primary(defined $primary ? $primary : 'sts'); |
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$self->source(defined $source ? $source : 'e-PCR'); |
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$self->groupclass(defined $groupclass ? $groupclass : 'name'); |
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$self->_initialize_io(@args); |
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return $self; |
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} |
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=head2 next_feature |
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Title : next_feature |
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Usage : $seqfeature = $obj->next_feature(); |
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Function: Returns the next feature available in the analysis result, or |
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undef if there are no more features. |
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Example : |
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Returns : A Bio::SeqFeatureI implementing object, or undef if there are no |
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more features. |
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Args : none |
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=cut |
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sub next_feature { |
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my ($self) = @_; |
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my $line = $self->_readline; |
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return unless defined($line); |
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chomp($line); |
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my($seqname,$location,$mkrname, $rest) = split(/\s+/,$line,4); |
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my ($start,$end) = ($location =~ /(\S+)\.\.(\S+)/); |
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# `e-PCR -direct` results code match strand in $rest as (+) and (-). Decode it if present. |
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my $strandsign; |
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if ($rest =~ m/^\(([+-])\)(.*)$/) { |
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($strandsign,$rest) = ($1, $2); |
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} else { |
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$strandsign = "?"; |
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} |
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my $strand = $strandsign eq "+" ? 1 : $strandsign eq "-" ? -1 : 0; |
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my $markerfeature = Bio::SeqFeature::Generic->new |
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( '-start' => $start, |
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'-end' => $end, |
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'-strand' => $strand, |
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'-source' => $self->source, |
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'-primary' => $self->primary, |
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'-seq_id' => $seqname, |
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'-tag' => { |
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$self->groupclass => $mkrname, |
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($rest ? ('Note' => $rest ) : ()), |
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}); |
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#$markerfeature->add_tag_value('Note', $rest) if defined $rest; |
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return $markerfeature; |
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} |
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=head2 source |
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Title : source |
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Usage : $obj->source($newval) |
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Function: |
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Example : |
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Returns : value of source (a scalar) |
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Args : on set, new value (a scalar or undef, optional) |
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=cut |
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sub source{ |
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my $self = shift; |
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return $self->{'_source'} = shift if @_; |
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return $self->{'_source'}; |
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} |
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=head2 primary |
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Title : primary |
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Usage : $obj->primary($newval) |
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Function: |
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Example : |
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Returns : value of primary (a scalar) |
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Args : on set, new value (a scalar or undef, optional) |
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=cut |
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sub primary{ |
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my $self = shift; |
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return $self->{'_primary'} = shift if @_; |
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return $self->{'_primary'}; |
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} |
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=head2 groupclass |
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227
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Title : groupclass |
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Usage : $obj->groupclass($newval) |
229
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Function: |
230
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Example : |
231
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Returns : value of groupclass (a scalar) |
232
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Args : on set, new value (a scalar or undef, optional) |
233
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234
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235
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=cut |
236
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237
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sub groupclass{ |
238
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16
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16
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1
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12
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my $self = shift; |
239
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240
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16
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100
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28
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return $self->{'_groupclass'} = shift if @_; |
241
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14
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61
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return $self->{'_groupclass'}; |
242
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} |
243
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244
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1; |