annotate variant_effect_predictor/Bio/Align/Utilities.pm @ 0:1f6dce3d34e0

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author mahtabm
date Thu, 11 Apr 2013 02:01:53 -0400
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1 # $Id: Utilities.pm,v 1.8 2002/11/11 18:39:19 jason Exp $
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2 #
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3 # BioPerl module for Bio::Align::Utilities
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4 #
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5 # Cared for by Jason Stajich <jason@bioperl.org>
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6 #
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7 # Copyright Jason Stajich
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8 #
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9 # You may distribute this module under the same terms as perl itself
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10
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11 # POD documentation - main docs before the code
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12
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13 =head1 NAME
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14
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15 Bio::Align::Utilities - A collection of utilities regarding converting and manipulating alignment objects
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16
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17 =head1 SYNOPSIS
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18
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19 use Bio::Align::Utilities qw(aa_to_dna_aln);
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20
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21 my $dna_aln = aa_to_dna_aln($aaaln,\%dnaseqs);
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22
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23
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24 =head1 DESCRIPTION
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25
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26 This module contains utility methods for manipulating sequence
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27 alignments ( L<Bio::Align::AlignI>) objects.
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28
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29 The B<aa_to_dna_aln> utility is essentially the same as the B<mrtrans>
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30 program by Bill Pearson available at
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31 ftp://ftp.virginia.edu/pub/fasta/other/mrtrans.shar. Of course this
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32 is a pure-perl implementation, but just to mention that if anything
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33 seems odd you can check the alignments generated against Bill's
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34 program.
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35
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36 =head1 FEEDBACK
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37
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38 =head2 Mailing Lists
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39
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40 User feedback is an integral part of the evolution of this and other
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41 Bioperl modules. Send your comments and suggestions preferably to
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42 the Bioperl mailing list. Your participation is much appreciated.
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43
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44 bioperl-l@bioperl.org - General discussion
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45 http://bioperl.org/MailList.shtml - About the mailing lists
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46
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47 =head2 Reporting Bugs
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48
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49 Report bugs to the Bioperl bug tracking system to help us keep track
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50 of the bugs and their resolution. Bug reports can be submitted via
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51 email or the web:
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52
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53 bioperl-bugs@bioperl.org
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54 http://bugzilla.bioperl.org/
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55
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56 =head1 AUTHOR - Jason Stajich
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57
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58 Email jason@bioperl.org
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59
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60 =head1 CONTRIBUTORS
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61
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62 Additional contributors names and emails here
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63
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64 =head1 APPENDIX
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65
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66 The rest of the documentation details each of the object methods.
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67 Internal methods are usually preceded with a _
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68
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69 =cut
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70
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71 #' keep my emacs happy
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72 # Let the code begin...
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73
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74
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75 package Bio::Align::Utilities;
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76 use vars qw(@ISA @EXPORT @EXPORT_OK);
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77 use strict;
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78 use Carp;
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79 require Exporter;
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80
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81 @ISA = qw(Exporter);
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82
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83 @EXPORT = qw();
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84 @EXPORT_OK = qw(aa_to_dna_aln);
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85
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86 use constant CODONSIZE => 3;
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87
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88 =head2 aa_to_dna_aln
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89
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90 Title : aa_to_dna_aln
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91 Usage : my $dnaaln = aa_to_dna_aln($aa_aln, \%seqs);
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92 Function: Will convert an AA alignment to DNA space given the
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93 corresponding DNA sequences. Note that this method expects
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94 the DNA sequences to be in frame +1 (GFF frame 0) as it will
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95 start to project into coordinates starting at the first base of
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96 the DNA sequence, if this alignment represents a different
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97 frame for the cDNA you will need to edit the DNA sequences
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98 to remove the 1st or 2nd bases (and revcom if things should be).
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99 Returns : Bio::Align::AlignI object
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100 Args : 2 arguments, the alignment and a hashref.
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101 Alignment is a Bio::Align::AlignI of amino acid sequences.
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102 The hash reference should have keys which are
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103 the display_ids for the aa
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104 sequences in the alignment and the values are a
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105 Bio::PrimarySeqI object for the corresponding
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106 spliced cDNA sequence.
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107
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108 See also: L<Bio::Align::AlignI>, L<Bio::SimpleAlign>, L<Bio::PrimarySeq>
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109
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110 =cut
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111
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112 sub aa_to_dna_aln {
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113 my ($aln,$dnaseqs) = @_;
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114 unless( defined $aln &&
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115 ref($aln) &&
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116 $aln->isa('Bio::Align::AlignI') ) {
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117 croak('Must provide a valid Bio::Align::AlignI object as the first argument to aa_to_dna_aln, see the documentation for proper usage and the method signature');
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118 }
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119 my $alnlen = $aln->length;
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120 #print "HSP length is $alnlen\n";
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121 my $dnaalign = new Bio::SimpleAlign;
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122 foreach my $seq ( $aln->each_seq ) {
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123 my $newseq;
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124 my $dnaseq = $dnaseqs->{$seq->display_id} || croak("cannot find ".
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125 $seq->display_id);
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126 foreach my $pos ( 1..$alnlen ) {
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127 my $loc = $seq->location_from_column($pos);
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128 my $dna = '';
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129 if( !defined $loc || $loc->location_type ne 'EXACT' ) {
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130 $dna = '---';
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131 } else {
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132 # To readjust to codon boundaries
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133 # end needs to be +1 so we can just multiply by CODONSIZE
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134 # to get this
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135
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136 my ($start,$end) = ((($loc->start - 1)* CODONSIZE) +1,
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137 ($loc->end)* CODONSIZE);
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138
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139 if( $start <=0 || $end > $dnaseq->length() ) {
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140 print STDERR "start is ", $loc->start, " end is ", $loc->end, " while dnaseq length is ", $dnaseq->length(), " and start/end projected are $start,$end \n";
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141 warn("codons don't seem to be matching up for $start,$end");
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142 $dna = '---';
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143 } else {
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144 $dna = $dnaseq->subseq($start,$end);
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145 }
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146 }
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147 $newseq .= $dna;
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148 }
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149 # funky looking math is to readjust to codon boundaries and deal
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150 # with fact that sequence start with 1
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151 my $newdna = new Bio::LocatableSeq(-display_id => $seq->id(),
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152 -start => (($seq->start - 1) *
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153 CODONSIZE) + 1,
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154 -end => ($seq->end * CODONSIZE),
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155 -strand => $seq->strand,
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156 -seq => $newseq);
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157 $dnaalign->add_seq($newdna);
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158 }
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159 return $dnaalign;
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160 }
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161 1;