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# BioPerl module for Bio::Restriction::IO::base |
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# |
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# Please direct questions and support issues to |
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# |
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# Cared for by Rob Edwards |
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# |
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# Copyright Rob Edwards |
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# |
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# You may distribute this module under the same terms as perl itself |
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# |
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# POD documentation - main docs before the code |
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=head1 NAME |
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Bio::Restriction::IO::base - base enzyme set |
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=head1 SYNOPSIS |
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Do not use this module directly. Use it via the Bio::Restriction::IO class. |
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=head1 DESCRIPTION |
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This class defines some base methods for restriction enzyme input and |
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at the same time gives a base list of common enzymes. |
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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 the |
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Bioperl mailing lists 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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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 |
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Rob Edwards, redwards@utmem.edu |
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=head1 CONTRIBUTORS |
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Heikki Lehvaslaiho, heikki-at-bioperl-dot-org |
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Mark A. Jensen, maj-at-fortinbras-dot-us |
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=head1 APPENDIX |
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The rest of the documentation details each of the object |
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methods. 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::Restriction::IO::base; |
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use strict; |
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use Bio::Restriction::Enzyme; |
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use Bio::Restriction::EnzymeCollection; |
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use Bio::Restriction::Enzyme::MultiCut; |
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use Bio::Restriction::Enzyme::MultiSite; |
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use base qw(Bio::Restriction::IO); |
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my $offset; # class variable |
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sub new { |
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my($class, @args) = @_; |
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$class = ref $class ? ref $class : $class; |
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my $self = bless {}, $class; |
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$self->_initialize(@args); |
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return $self; |
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} |
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{ |
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my %FILE_FORMAT = ( |
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#'itype2' => 'itype2', # itype2 format doesn't work with 'current' |
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#'8' => 'itype2', |
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'withrefm' => 'withrefm', |
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'31' => 'withrefm', |
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#'bairoch' => 'bairoch', # bairoch format doesn't work with 'current' |
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#'19' => 'bairoch', |
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#'macvector' => 'bairoch', |
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#'vectorNTI' => 'bairoch', |
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'neo' => 'neos', |
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'prototype' => 'proto' |
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); |
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sub _initialize { |
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my($self,@args) = @_; |
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my ($current, $url, $file, $fh, $format, $verbose) = |
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$self->_rearrange([qw(CURRENT URL FILE FH FORMAT VERBOSE)],@args); |
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$verbose || 0; |
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$self->verbose($verbose); |
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if ($current && $format) { |
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$self->throw("Can't use -current with file, fh, or url set") if ($url || $file || $fh); |
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$self->throw("Format $format not retrievable using 'current'") if (!exists $FILE_FORMAT{$format}); |
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my $io = $self->new(-url => 'ftp://ftp.neb.com/pub/rebase/VERSION'); |
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chomp (my $version = $io->_readline); |
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push @args, (-url => "ftp://ftp.neb.com/pub/rebase/$FILE_FORMAT{$format}.$version", -retries => 1); |
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} |
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$self->_companies; |
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return unless $self->SUPER::_initialize(@args); |
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} |
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} |
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=head2 read |
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Title : read |
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Usage : $renzs = $stream->read |
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Function: reads all the restrction enzymes from the stream |
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Returns : a Bio::Restriction::Restriction object |
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Args : none |
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142
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=cut |
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144
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sub read { |
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my $self = shift; |
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147
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my $renzs = Bio::Restriction::EnzymeCollection->new(-empty => 1); |
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seek DATA,($offset||=tell DATA), 0; |
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while () { |
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chomp; |
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next if /^\s*$/; |
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my ($name, $site, $cut) = split /\s+/; |
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my $re = Bio::Restriction::Enzyme->new(-name => $name, |
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-site => $site, |
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-cut => $cut); |
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6091
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$renzs->enzymes($re); |
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} |
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return $renzs; |
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} |
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161
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=head2 _xln_sub |
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163
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Title : _xln_sub |
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Function: Translates withrefm coords to Bio::Restriction coords |
165
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Args : Bio::Restriction::Enzyme object, scalar integer (cut posn) |
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Note : Used internally; pass as a coderef to the B:R::Enzyme |
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constructor |
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Note : It is convenient for each format module to have its own |
169
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version of this; not currently demanded by the interface. |
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=cut |
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172
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sub _xln_sub { # for base.pm, a no-op |
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0
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0
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my ($z,$c) = @_; |
174
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0
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0
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return $c; |
175
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} |
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177
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178
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=head2 write |
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180
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Title : write |
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Usage : $stream->write($renzs) |
182
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Function: writes restriction enzymes into the stream |
183
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Returns : 1 for success and 0 for error |
184
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Args : a Bio::Restriction::Enzyme |
185
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or a Bio::Restriction::EnzymeCollection object |
186
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187
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=cut |
188
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189
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sub write { |
190
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0
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0
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1
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0
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my $self = shift; |
191
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0
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0
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foreach (@_) { |
192
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0
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0
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map { printf "%s\t%s\t%s\n", $_->name, $_->string, $_->cut |
193
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0
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0
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} sort {$a->name cmp $b->name} $_->each_enzyme |
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0
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194
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if $_->isa('Bio::Restriction::EnzymeCollection'); |
195
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0
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0
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0
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printf "%s\t%s\t%s\n", $_->name, $_->string, $_->cut |
196
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if $_->isa('Bio::Restriction::Enzyme'); |
197
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} |
198
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} |
199
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200
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=head2 verify_prototype |
201
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202
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Title : verify_prototype |
203
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Purpose : checks enzyme against current prototype list (retrieved remotely) |
204
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Returns : returns TRUE if enzyme is prototype |
205
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Argument : Bio::Restriction::EnzymeI |
206
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Comments : This is an auxiliary method to retrieve and check an enzyme |
207
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as a prototype. It retrieves the current list, stores it |
208
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as a singleton instance, then uses it to check the prototype |
209
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and modify is_prototype() to true or false. Use as follows: |
210
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211
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my $col = $io->read; |
212
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for my $enz ($col->each_enzyme) { |
213
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print $enz->name.":".$enz->site."\n"; |
214
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print "\t".$io->verify_prototype($enz)."\n"; |
215
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} |
216
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217
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=cut |
218
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219
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my $protodb; |
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sub verify_prototype { |
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my ($self, $enz) = @_; |
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$self->throw("Must pass a Bio::Restriction::EnzymeI") unless |
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$enz && ref $enz && $enz->isa("Bio::Restriction::EnzymeI"); |
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if (!defined $protodb) { |
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my $io = Bio::Restriction::IO->new(-format => 'prototype', |
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-current => 1); |
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$protodb = $io->read; |
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} |
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if ($protodb->get_enzyme($enz->name)) { |
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$enz->is_prototype(1); |
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} else { |
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$enz->is_prototype(0); |
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} |
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$enz->is_prototype; |
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} |
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=head2 Common REBASE parsing methods |
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The rest of the methods in this file are to be used by other REBASE |
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parsers. They are not to be used outside subclasses of this base |
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class. (They are 'protected' in the sense the word is used in Java.) |
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=cut |
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246
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=head2 _cuts_from_site |
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248
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Title : _cuts_from_site |
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Usage : ($site, $cut, $comp_cut) = _cuts_from_site('ACGCGT(4/5)'); |
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Function: Separates cut positions from a single site string. |
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Does nothing to site if it does not have the cut string |
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Returns : array of site_string, forward_cut_position, reverse_cut_position |
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Args : recognition site string |
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Note : Not used in withrefm refactor/maj |
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256
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=cut |
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258
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sub _cuts_from_site { |
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0
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my ($self, $site) = @_; |
260
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my ($cut, $comp_cut) = $site =~ /\((-?\d+)\/(-?\d+)\)/; |
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0
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$site =~ s/\(.*\)$//; |
262
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return ($site, $cut, $comp_cut); |
263
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} |
264
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265
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266
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=head2 _meth |
267
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268
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Title : _meth |
269
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Usage : ($pos, $meth) = $self->_meth('2(5)'); |
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Function: Separates methylation postion and coce from a string. |
271
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Adjusts the postion depending on enzyme site length |
272
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and symmetry |
273
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Returns : array of position and methylation code |
274
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Args : 1. reference to Enzyme object |
275
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2. methylation description string |
276
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277
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=cut |
278
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279
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sub _meth { |
280
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828
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828
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1296
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my ($self, $re, $meth) = @_; |
281
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282
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828
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708
|
$meth =~ /(\S+)\((\d+)\)/; |
283
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828
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885
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my ($pos, $m) = ($1, $2); |
284
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828
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100
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1327
|
$pos = 0 if $pos eq '?'; |
285
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828
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100
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100
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1740
|
$pos = $re->seq->length + $pos if $pos and ! $re->palindromic; |
286
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828
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1854
|
return ($pos, $m); |
287
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288
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0
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0
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0
|
$self->warn("Unknown methylation format [$meth]") if $self->verbose >0; |
289
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|
} |
290
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291
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292
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=head2 _coordinate_shift_to_cut |
293
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294
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|
Title : _coordinate_shift_to_cut |
295
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|
Usage : $cut = $self->_coordinate_shift_to_cut($oricut, offset); |
296
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|
Function: Adjust cut position coordinates to start from the |
297
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first nucleotides of site |
298
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|
Returns : Cut position in correct coordinates |
299
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|
Args : 1. Original cut position |
300
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|
2. Length of the recognition site |
301
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|
Note : Not used in withrefm.pm refactor/maj |
302
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303
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|
=cut |
304
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305
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|
|
sub _coordinate_shift_to_cut { |
306
|
0
|
|
|
0
|
|
0
|
my ($self, $cut, $site_length) = @_; |
307
|
0
|
|
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|
|
0
|
return $cut + $site_length; |
308
|
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|
|
} |
309
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310
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311
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|
=head2 _make_multisites |
312
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313
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|
Title : _make_multisites |
314
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|
|
Usage : $self->_make_multisites($first_enzyme, \@sites, \@mets) |
315
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|
|
Function: Bless a Bio::Restriction::Enzyme into |
316
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|
Bio::Restriction::Enzyme::MultiSite and clone it as many |
317
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|
times as there are alternative sites. |
318
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|
Returns : nothing, does in place editing |
319
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|
|
Args : 1. a Bio::Restriction::Enzyme |
320
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|
|
2. reference to an array of recognition site strings |
321
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|
|
3. reference to an array of methylation code strings, optional |
322
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323
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|
=cut |
324
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325
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|
|
# removed the enzyme collection from arg list /maj |
326
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327
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|
|
|
sub _make_multisites { |
328
|
15
|
|
|
15
|
|
22
|
my ($self, $re, $sites, $meths, $xln_sub) = @_; |
329
|
|
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|
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|
330
|
15
|
|
|
|
|
47
|
bless $re, 'Bio::Restriction::Enzyme::MultiSite'; |
331
|
|
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332
|
15
|
|
|
|
|
20
|
my $count = 0; |
333
|
15
|
|
|
|
|
21
|
while ($count < scalar @{$sites}) { |
|
41
|
|
|
|
|
85
|
|
334
|
|
|
|
|
|
|
# this should probably be refactored to use the constructor |
335
|
|
|
|
|
|
|
# too, rather than the clone/accessor method /maj |
336
|
|
|
|
|
|
|
# my $re2 = $re->clone; |
337
|
|
|
|
|
|
|
# my $re2; |
338
|
|
|
|
|
|
|
|
339
|
26
|
|
|
|
|
27
|
my $site = @{$sites}[$count]; |
|
26
|
|
|
|
|
40
|
|
340
|
26
|
|
|
|
|
107
|
my ($precut, $recog, $postcut) = ( $site =~ m/^(?:\((\w+\/\w+)\))?([\w^]+)(?:\((\w+\/\w+)\))?/ ); |
341
|
|
|
|
|
|
|
|
342
|
|
|
|
|
|
|
# set the site attribute |
343
|
|
|
|
|
|
|
# $re2->site($recog); |
344
|
|
|
|
|
|
|
|
345
|
|
|
|
|
|
|
# set the recog attribute (which will make the regexp transformation |
346
|
|
|
|
|
|
|
# if necessary: |
347
|
|
|
|
|
|
|
# $re2->recog($recog); |
348
|
|
|
|
|
|
|
# $recog = $re2->string; |
349
|
|
|
|
|
|
|
|
350
|
|
|
|
|
|
|
# no warnings; # avoid 'uninitialized value' warning against $postcut |
351
|
|
|
|
|
|
|
# my ($cut, $comp_cut) = ( $postcut =~ /(-?\d+)\/(-?\d+)/ ); |
352
|
|
|
|
|
|
|
# use warnings; |
353
|
|
|
|
|
|
|
|
354
|
|
|
|
|
|
|
# note the following hard codes the coordinate transformation |
355
|
|
|
|
|
|
|
# used for rebase/itype2 : this method will break on the |
356
|
|
|
|
|
|
|
# base.pm format. |
357
|
|
|
|
|
|
|
# if ($cut) { |
358
|
|
|
|
|
|
|
# $re2->cut($cut + length $recog); |
359
|
|
|
|
|
|
|
# $re2->complementary_cut($comp_cut + length $recog); |
360
|
|
|
|
|
|
|
# } |
361
|
|
|
|
|
|
|
|
362
|
26
|
|
|
|
|
78
|
my $re2 = Bio::Restriction::Enzyme::MultiSite->new( |
363
|
|
|
|
|
|
|
-name => $re->name, |
364
|
|
|
|
|
|
|
-site => $recog, |
365
|
|
|
|
|
|
|
-recog => $recog, |
366
|
|
|
|
|
|
|
-precut => $precut, |
367
|
|
|
|
|
|
|
-postcut => $postcut, |
368
|
|
|
|
|
|
|
-xln_sub => $xln_sub |
369
|
|
|
|
|
|
|
); |
370
|
|
|
|
|
|
|
|
371
|
26
|
100
|
66
|
|
|
107
|
if ($meths and @$meths) { |
372
|
22
|
|
|
|
|
48
|
$re2->purge_methylation_sites; |
373
|
22
|
|
|
|
|
25
|
$re2->methylation_sites($self->_meth($re2, @{$meths}[$count])); |
|
22
|
|
|
|
|
46
|
|
374
|
|
|
|
|
|
|
} |
375
|
|
|
|
|
|
|
|
376
|
26
|
|
|
|
|
75
|
$re->others($re2); |
377
|
26
|
|
|
|
|
31
|
$count++; |
378
|
|
|
|
|
|
|
} |
379
|
|
|
|
|
|
|
|
380
|
15
|
|
|
|
|
39
|
foreach my $enz ($re->others) { |
381
|
26
|
|
|
|
|
44
|
$enz->others($re, grep {$_ ne $enz} $re->others); |
|
66
|
|
|
|
|
116
|
|
382
|
|
|
|
|
|
|
} |
383
|
|
|
|
|
|
|
|
384
|
15
|
|
|
|
|
22
|
1; |
385
|
|
|
|
|
|
|
} |
386
|
|
|
|
|
|
|
|
387
|
|
|
|
|
|
|
=head2 _make_multicuts |
388
|
|
|
|
|
|
|
|
389
|
|
|
|
|
|
|
Title : _make_multicuts |
390
|
|
|
|
|
|
|
Usage : $self->_make_multicuts($first_enzyme, $precuts) |
391
|
|
|
|
|
|
|
Function: |
392
|
|
|
|
|
|
|
|
393
|
|
|
|
|
|
|
Bless a Bio::Restriction::Enzyme into |
394
|
|
|
|
|
|
|
Bio::Restriction::Enzyme::MultiCut and clone it. The precut |
395
|
|
|
|
|
|
|
string is processed to replase the cut sites in the cloned |
396
|
|
|
|
|
|
|
object. Both objects refer to each other through others() method. |
397
|
|
|
|
|
|
|
|
398
|
|
|
|
|
|
|
Returns : nothing, does in place editing |
399
|
|
|
|
|
|
|
Args : 1. a Bio::Restriction::Enzyme |
400
|
|
|
|
|
|
|
2. precut string, e.g. '12/7' |
401
|
|
|
|
|
|
|
|
402
|
|
|
|
|
|
|
|
403
|
|
|
|
|
|
|
The examples we have of multiply cutting enzymes cut only four |
404
|
|
|
|
|
|
|
times. This protected method deals only with a string of two |
405
|
|
|
|
|
|
|
integers separated with a slash, e.g. '12/7'. The numbers represent the postions |
406
|
|
|
|
|
|
|
BEFORE the start of the recognition site, i.e. negative positions. |
407
|
|
|
|
|
|
|
|
408
|
|
|
|
|
|
|
=cut |
409
|
|
|
|
|
|
|
|
410
|
|
|
|
|
|
|
# removed the enzyme collection from arg list /maj |
411
|
|
|
|
|
|
|
|
412
|
|
|
|
|
|
|
sub _make_multicuts { |
413
|
0
|
|
|
0
|
|
0
|
my ($self, $re, $precut) = @_; |
414
|
|
|
|
|
|
|
|
415
|
0
|
|
|
|
|
0
|
bless $re, 'Bio::Restriction::Enzyme::MultiCut'; |
416
|
|
|
|
|
|
|
|
417
|
0
|
|
|
|
|
0
|
my ($cut, $comp_cut) = $precut =~ /(-?\d+)\/(-?\d+)/; |
418
|
|
|
|
|
|
|
|
419
|
0
|
|
|
|
|
0
|
my $re2 = $re->clone; |
420
|
|
|
|
|
|
|
|
421
|
0
|
|
|
|
|
0
|
$re2->cut("-$cut"); |
422
|
0
|
|
|
|
|
0
|
$re2->complementary_cut("-$comp_cut"); |
423
|
|
|
|
|
|
|
|
424
|
0
|
|
|
|
|
0
|
$re->others($re2); |
425
|
|
|
|
|
|
|
|
426
|
0
|
|
|
|
|
0
|
1; |
427
|
|
|
|
|
|
|
} |
428
|
|
|
|
|
|
|
|
429
|
|
|
|
|
|
|
=head2 _companies |
430
|
|
|
|
|
|
|
|
431
|
|
|
|
|
|
|
Title : _companies |
432
|
|
|
|
|
|
|
Purpose : Defines the companies that we know about |
433
|
|
|
|
|
|
|
Returns : A hash |
434
|
|
|
|
|
|
|
Argument : Nothing |
435
|
|
|
|
|
|
|
Comments : An internal method to define the companies that we know about |
436
|
|
|
|
|
|
|
REBASE uses a code, and this converts the code to the real name |
437
|
|
|
|
|
|
|
(e.g. A = Amersham Pharmacia Biotech) |
438
|
|
|
|
|
|
|
|
439
|
|
|
|
|
|
|
=cut |
440
|
|
|
|
|
|
|
|
441
|
|
|
|
|
|
|
sub _companies { |
442
|
|
|
|
|
|
|
# this is just so it is easy to set up the codes that REBASE uses |
443
|
11
|
|
|
11
|
|
16
|
my $self=shift; |
444
|
11
|
|
|
|
|
147
|
my %companies=( |
445
|
|
|
|
|
|
|
'A'=>'Amersham Pharmacia Biotech (1/03)', |
446
|
|
|
|
|
|
|
'C'=>'Minotech Biotechnology (6/01)', |
447
|
|
|
|
|
|
|
'E'=>'Stratagene (1/03)', |
448
|
|
|
|
|
|
|
'F'=>'Fermentas AB (1/03)', |
449
|
|
|
|
|
|
|
'G'=>'Qbiogene (1/03)', |
450
|
|
|
|
|
|
|
'H'=>'American Allied Biochemical, Inc. (10/98)', |
451
|
|
|
|
|
|
|
'I'=>'SibEnzyme Ltd. (1/03)', |
452
|
|
|
|
|
|
|
'J'=>'Nippon Gene Co., Ltd. (6/00)', |
453
|
|
|
|
|
|
|
'K'=>'Takara Shuzo Co. Ltd. (1/03)', |
454
|
|
|
|
|
|
|
'M'=>'Roche Applied Science (1/03)', |
455
|
|
|
|
|
|
|
'N'=>'New England Biolabs (1/03)', |
456
|
|
|
|
|
|
|
'O'=>'Toyobo Biochemicals (11/98)', |
457
|
|
|
|
|
|
|
'P'=>'Megabase Research Products (5/99)', |
458
|
|
|
|
|
|
|
'Q'=>'CHIMERx (1/03)', |
459
|
|
|
|
|
|
|
'R'=>'Promega Corporation (1/03)', |
460
|
|
|
|
|
|
|
'S'=>'Sigma Chemical Corporation (1/03)', |
461
|
|
|
|
|
|
|
'U'=>'Bangalore Genei (1/03)', |
462
|
|
|
|
|
|
|
'V'=>'MRC-Holland (1/03)', |
463
|
|
|
|
|
|
|
'X'=>'EURx Ltd. (1/03)'); |
464
|
11
|
|
|
|
|
23
|
$self->{company}=\%companies; |
465
|
|
|
|
|
|
|
} |
466
|
|
|
|
|
|
|
|
467
|
|
|
|
|
|
|
1; |
468
|
|
|
|
|
|
|
|
469
|
|
|
|
|
|
|
__DATA__ |