/usr/share/perl5/Bio/ClusterIO/unigene.pm is in libbio-perl-perl 1.6.923-1.
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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 | # BioPerl module for Bio::ClusterIO::unigene
#
# Please direct questions and support issues to <bioperl-l@bioperl.org>
#
# Cared for by Andrew Macgregor <andrew at cbbc.murdoch.edu.au>
#
# Copyright Andrew Macgregor, Jo-Ann Stanton, David Green
# Molecular Embryology Group, Anatomy & Structural Biology, University of Otago
# http://meg.otago.ac.nz
#
# You may distribute this module under the same terms as perl itself
#
# _history
# April 17, 2002 - Initial implementation by Andrew Macgregor
# POD documentation - main docs before the code
=head1 NAME
Bio::ClusterIO::unigene - UniGene input stream
=head1 SYNOPSIS
Do not use this module directly. Use it via the Bio::ClusterIO class.
=head1 DESCRIPTION
This object reads from Unigene *.data files downloaded from
ftp://ftp.ncbi.nih.gov/repository/UniGene/. It does not download and
decompress the file, you have to do that yourself.
=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 one
of the Bioperl mailing lists. 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<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.
=head2 Reporting Bugs
Report bugs to the Bioperl bug tracking system to help us keep track
the bugs and their resolution. Bug reports can be submitted via the
web:
https://redmine.open-bio.org/projects/bioperl/
=head1 AUTHORS - Andrew Macgregor
Email: andrew at cbbc.murdoch.edu.au
=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::ClusterIO::unigene;
use strict;
use Bio::Cluster::UniGene;
use Bio::Cluster::ClusterFactory;
use base qw(Bio::ClusterIO);
my %line_is = (
ID => q/ID\s+(\w{2,3}\.\d+)/,
TITLE => q/TITLE\s+(\S.*)/,
GENE => q/GENE\s+(\S.*)/,
CYTOBAND => q/CYTOBAND\s+(\S.*)/,
MGI => q/MGI\s+(\S.*)/,
LOCUSLINK => q/LOCUSLINK\s+(\S.*)/,
HOMOL => q/HOMOL\s+(\S.*)/,
EXPRESS => q/EXPRESS\s+(\S.*)/,
RESTR_EXPR => q/RESTR_EXPR\s+(\S.*)/,
GNM_TERMINUS => q/GNM_TERMINUS\s+(\S.*)/,
CHROMOSOME => q/CHROMOSOME\s+(\S.*)/,
STS => q/STS\s+(\S.*)/,
TXMAP => q/TXMAP\s+(\S.*)/,
PROTSIM => q/PROTSIM\s+(\S.*)/,
SCOUNT => q/SCOUNT\s+(\S.*)/,
SEQUENCE => q/SEQUENCE\s+(\S.*)/,
ACC => q/ACC=(\w+)(\.\d+)?/,
NID => q/NID=\s*(\S.*)/,
PID => q/PID=\s*(\S.*)/,
CLONE => q/CLONE=\s*(\S.*)/,
END => q/END=\s*(\S.*)/,
LID => q/LID=\s*(\S.*)/,
MGC => q/MGC=\s*(\S.*)/,
SEQTYPE => q/SEQTYPE=\s*(\S.*)/,
TRACE => q/TRACE=\s*(\S.*)/,
PERIPHERAL => q/PERIPHERAL=\s*(\S.*)/,
DELIMITER => q{^//},
);
# we set the right factory here
sub _initialize {
my($self, @args) = @_;
$self->SUPER::_initialize(@args);
if(! $self->cluster_factory()) {
$self->cluster_factory(Bio::Cluster::ClusterFactory->new(
-type => 'Bio::Cluster::UniGene'));
}
}
=head2 next_cluster
Title : next_cluster
Usage : $unigene = $stream->next_cluster()
Function: returns the next unigene in the stream
Returns : Bio::Cluster::UniGene object
Args : NONE
=cut
sub next_cluster {
my( $self) = @_;
local $/ = "\n//";
return unless my $entry = $self->_readline;
# set up the variables we'll need
my (%unigene,@express,@locuslink,@chromosome,
@sts,@txmap,@protsim,@sequence);
my $UGobj;
# set up the regexes
# add whitespace parsing and precompile regexes
#foreach (values %line_is) {
# $_ =~ s/\s+/\\s+/g;
# print STDERR "Regex is $_\n";
# #$_ = qr/$_/x;
#}
#$line_is{'TITLE'} = qq/TITLE\\s+(\\S.+)/;
# run each line in an entry against the regexes
foreach my $line (split /\n/, $entry) {
#print STDERR "Wanting to match $line\n";
if ($line =~ /$line_is{ID}/gcx) {
$unigene{ID} = $1;
}
elsif ($line =~ /$line_is{TITLE}/gcx ) {
#print STDERR "MATCHED with [$1]\n";
$unigene{TITLE} = $1;
}
elsif ($line =~ /$line_is{GENE}/gcx) {
$unigene{GENE} = $1;
}
elsif ($line =~ /$line_is{CYTOBAND}/gcx) {
$unigene{CYTOBAND} = $1;
}
elsif ($line =~ /$line_is{MGI}/gcx) {
$unigene{MGI} = $1;
}
elsif ($line =~ /$line_is{LOCUSLINK}/gcx) {
@locuslink = split /;/, $1;
}
elsif ($line =~ /$line_is{HOMOL}/gcx) {
$unigene{HOMOL} = $1;
}
elsif ($line =~ /$line_is{EXPRESS}/gcx) {
my $express = $1;
# remove initial semicolon if present
$express =~ s/^;//;
@express = split /\s*;/, $express;
}
elsif ($line =~ /$line_is{RESTR_EXPR}/gcx) {
$unigene{RESTR_EXPR} = $1;
}
elsif ($line =~ /$line_is{GNM_TERMINUS}/gcx) {
$unigene{GNM_TERMINUS} = $1;
}
elsif ($line =~ /$line_is{CHROMOSOME}/gcx) {
push @chromosome, $1;
}
elsif ($line =~ /$line_is{TXMAP}/gcx) {
push @txmap, $1;
}
elsif ($line =~ /$line_is{STS}/gcx) {
push @sts, $1;
}
elsif ($line =~ /$line_is{PROTSIM}/gcx) {
push @protsim, $1;
}
elsif ($line =~ /$line_is{SCOUNT}/gcx) {
$unigene{SCOUNT} = $1;
}
elsif ($line =~ /$line_is{SEQUENCE}/gcx) {
# parse into each sequence line
my $seq = {};
# add unigene id to each seq
#$seq->{unigene_id} = $unigene{ID};
my @items = split(/;/, $1);
foreach (@items) {
if (/$line_is{ACC}/gcx) {
$seq->{acc} = $1;
# remove leading dot if version pattern matched
$seq->{version} = substr($2,1) if defined $2;
}
elsif (/$line_is{NID}/gcx) {
$seq->{nid} = $1;
}
elsif (/$line_is{PID}/gcx) {
$seq->{pid} = $1;
}
elsif (/$line_is{CLONE}/gcx) {
$seq->{clone} = $1;
}
elsif (/$line_is{END}/gcx) {
$seq->{end} = $1;
}
elsif (/$line_is{LID}/gcx) {
$seq->{lid} = $1;
}
elsif (/$line_is{MGC}/gcx) {
$seq->{mgc} = $1;
}
elsif (/$line_is{SEQTYPE}/gcx) {
$seq->{seqtype} = $1;
}
elsif (/$line_is{TRACE}/gcx) {
$seq->{trace} = $1;
}
elsif (/$line_is{PERIPHERAL}/gcx) {
$seq->{peripheral} = $1;
}
}
push @sequence, $seq;
}
elsif ($line =~ /$line_is{DELIMITER}/gcx) {
# at the end of the record, add data to the object
$UGobj = $self->cluster_factory->create_object(
-display_id => $unigene{ID},
-description => $unigene{TITLE},
-size => $unigene{SCOUNT},
-members => \@sequence);
$UGobj->gene($unigene{GENE}) if defined ($unigene{GENE});
$UGobj->cytoband($unigene{CYTOBAND}) if defined($unigene{CYTOBAND});
$UGobj->mgi($unigene{MGI}) if defined ($unigene{MGI});
$UGobj->locuslink(\@locuslink);
$UGobj->homol($unigene{HOMOL}) if defined ($unigene{HOMOL});
$UGobj->express(\@express);
$UGobj->restr_expr($unigene{RESTR_EXPR}) if defined ($unigene{RESTR_EXPR});
$UGobj->gnm_terminus($unigene{GNM_TERMINUS}) if defined ($unigene{GNM_TERMINUS});
$UGobj->chromosome(\@chromosome);
$UGobj->sts(\@sts);
$UGobj->txmap(\@txmap);
$UGobj->protsim(\@protsim);
}
}
return $UGobj;
}
1;
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