line |
stmt |
bran |
cond |
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code |
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package Bio::MUST::Core::Seq; |
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# ABSTRACT: Nucleotide or protein sequence |
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# CONTRIBUTOR: Catherine COLSON <ccolson@doct.uliege.be> |
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# CONTRIBUTOR: Arnaud DI FRANCO <arnaud.difranco@gmail.com> |
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# CONTRIBUTOR: Valerian LUPO <valerian.lupo@doct.uliege.be> |
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$Bio::MUST::Core::Seq::VERSION = '0.212670'; |
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132
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use Moose; |
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47
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138
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8
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97172
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use MooseX::SemiAffordanceAccessor; |
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140197
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137647
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use namespace::autoclean; |
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43
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186
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# use Smart::Comments '###'; |
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1899
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use autodie; |
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41
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390
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93832
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use feature qw(say); |
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1842
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use Carp; |
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1522
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use Bio::MUST::Core::Types; |
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564
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use Bio::MUST::Core::Constants qw(:seqtypes :seqids :gaps); |
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4602
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10074
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use aliased 'Bio::MUST::Core::SeqId'; |
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13836
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has 'seq_id' => ( |
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is => 'rw', |
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isa => 'Bio::MUST::Core::SeqId', |
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required => 1, |
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coerce => 1, |
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handles => qr{.*}xms, # expose all SeqId methods (and attributes) |
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); |
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has 'seq' => ( |
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traits => ['String'], |
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is => 'ro', |
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isa => 'Bio::MUST::Core::Types::Seq', |
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default => q{}, # can be empty |
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coerce => 1, |
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writer => '_set_seq', |
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handles => { |
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seq_len => 'length', |
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append_seq => 'append', |
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replace_seq => 'replace', |
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edit_seq => 'substr', |
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}, |
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); |
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48
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# TODO: check whether this could be done by some Moose extension |
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50
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sub clone { |
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402
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402
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1
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694
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my $self = shift; |
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53
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402
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1172
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return $self->new( |
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seq_id => $self->full_id, seq => $self->seq |
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); |
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} |
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58
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59
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# boolean assertions |
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# TODO: optimize these assertions via caching |
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62
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63
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sub is_protein { |
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643
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643
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1
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962
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my $self = shift; |
65
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643
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100
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16912
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return 1 if $self->seq =~ $PROTLIKE; |
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153
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461
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return 0; # at least 1 non-nt char |
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} |
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69
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70
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sub is_rna { |
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11
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11
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1
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26
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my $self = shift; |
72
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11
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100
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100
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276
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return 1 if $self->seq =~ $RNALIKE && (not $self->is_protein); |
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9
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43
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return 0; # at least 1 'U' |
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} |
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76
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77
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sub is_aligned { |
78
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8599
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8599
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1
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10823
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my $self = shift; |
79
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8599
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100
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191079
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return 1 if $self->seq =~ $GAP; # at least 1 gap-like char |
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8403
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15808
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return 0; |
81
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} |
82
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83
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84
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sub is_subseq_of { |
85
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36
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36
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1
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81
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my $self = shift; |
86
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36
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58
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my $seq2 = shift; # can be a mere string |
87
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88
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36
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103
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$self = $self->raw_str; |
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36
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100
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239
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$seq2 = $seq2->isa('Bio::MUST::Core::Seq') |
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? $seq2->raw_str : _strip_gaps($seq2); |
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36
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100
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411
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return 1 if $seq2 =~ m/$self/xmsi; # case-insensitive comparison |
92
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16
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80
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return 0; # only here because expensive! |
93
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} |
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95
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96
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sub is_superseq_of { |
97
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36
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36
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1
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155
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my $self = shift; |
98
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36
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62
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my $seq2 = shift; # can be a mere string |
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100
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36
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77
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$self = $self->raw_str; |
101
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36
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100
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167
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$seq2 = $seq2->isa('Bio::MUST::Core::Seq') |
102
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? $seq2->raw_str : _strip_gaps($seq2); |
103
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36
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100
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303
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return 1 if $self =~ m/$seq2/xmsi; # case-insensitive comparison |
104
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16
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56
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return 0; # only here because expensive! |
105
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} |
106
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107
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108
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sub first_site { |
109
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11
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11
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1
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26
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my $self = shift; |
110
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111
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11
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276
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my ($leading_gaps) = $self->seq =~ m{ \A ($GAP+) }xms; |
112
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11
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100
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80
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return length $leading_gaps // 0; |
113
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} |
114
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115
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116
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sub uc { ## no critic (ProhibitBuiltinHomonyms) |
117
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5
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5
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1
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9
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my $self = shift; |
118
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119
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5
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129
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$self->_set_seq( uc $self->seq ); |
120
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5
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18
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return $self; |
121
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} |
122
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123
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sub uc_seq { ## no critic (RequireArgUnpacking) |
124
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0
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0
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0
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0
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carp '[BMC] Warning: Method uc_seq is deprecated; use uc instead!'; |
125
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0
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0
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return shift->uc(@_); |
126
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} |
127
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128
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129
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sub recode { |
130
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5
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5
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1
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10
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my $self = shift; |
131
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5
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10
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my $base_for = shift; |
132
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133
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5
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13
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my @states = $self->all_states; |
134
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5
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11
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my @rec_states; |
135
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136
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5
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11
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for my $state (@states) { |
137
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700
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33
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1202
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my $rec_state = $base_for->{$state} // $FRAMESHIFT; |
138
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700
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934
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push @rec_states, $rec_state; |
139
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} |
140
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141
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5
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33
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my $new_seq = join q{}, @rec_states; |
142
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5
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157
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$self->_set_seq($new_seq); |
143
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144
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5
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79
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return $self; |
145
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} |
146
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147
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sub recode_seq { ## no critic (RequireArgUnpacking) |
148
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0
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0
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0
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0
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carp '[BMC] Warning: Method recode_seq is deprecated; use recode instead!'; |
149
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0
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0
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return shift->recode(@_); |
150
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} |
151
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152
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# gap cleaning methods |
153
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154
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155
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sub degap { |
156
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38
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38
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1
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92
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my $self = shift; |
157
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158
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38
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166
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$self->_set_seq($self->raw_str); |
159
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38
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279
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return $self; |
160
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} |
161
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162
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163
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sub gapify { |
164
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71
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71
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1
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137
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my $self = shift; |
165
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71
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100
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202
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my $char = shift // '*'; # defaults to gap |
166
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167
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71
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128
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my $regex = $PROTMISS; # defaults to protein seq |
168
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169
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# in case of DNA ensure correct 'missification' (if applicable) |
170
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71
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100
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157
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unless ($self->is_protein) { |
171
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8
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14
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$regex = $DNAMISS; |
172
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8
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100
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33
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$char = 'N' if $char =~ $DNAMISS; |
173
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} |
174
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175
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71
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1801
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( my $seq = $self->seq ) =~ s{$regex}{$char}xmsg; |
176
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177
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# alternative versions developed due to a design error in Ali::store_phylip |
178
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# They are now commented because less general and not critical anymore. |
179
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180
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# alt vers 1: hard-coding $char (if possible) gives a 250% boost |
181
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# my $seq = $self->seq; |
182
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# if ($self->is_protein) { |
183
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# if ($char eq '*') { |
184
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# $seq =~ s{$PROTMISS}{*}xmsg; |
185
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# } |
186
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# elsif ($char eq 'X') { |
187
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# $seq =~ s{$PROTMISS}{X}xmsg; |
188
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# } |
189
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# else { |
190
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# $seq =~ s{$PROTMISS}{$char}xmsg; |
191
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# } |
192
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# } |
193
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# else { |
194
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# if ($char eq '*') { |
195
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# $seq =~ s{$DNAMISS}{*}xmsg; |
196
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# } |
197
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# elsif ($char eq 'X') { |
198
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# $seq =~ s{$DNAMISS}{N}xmsg; |
199
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# } |
200
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# else { |
201
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# $seq =~ s{$DNAMISS}{$char}xmsg; |
202
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# } |
203
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# } |
204
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205
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# alt vers 2: hard-coded tr/// for 900% boost with s/// fall-back |
206
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# Note: $PROTMISS and $DNAMISS regexes in Constants.pm are ignored! |
207
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# my $seq = $self->seq; |
208
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# if ($self->is_protein) { |
209
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# if ($char eq '*') { |
210
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# $seq =~ tr{?XxBJOUZbjouz}{*}; |
211
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# } |
212
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# elsif ($char eq 'X') { |
213
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# $seq =~ tr{?XxBJOUZbjouz}{X}; |
214
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# } |
215
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# else { |
216
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# $seq =~ s{[?XxBJOUZbjouz]}{$char}xmsg; |
217
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# } |
218
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# } |
219
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# else { |
220
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# if ($char eq '*') { |
221
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# $seq =~ tr{?XxNnBDHKMRSVWYbdhkmrsvwy}{*}; |
222
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# } |
223
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# elsif ($char eq 'X') { |
224
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# $seq =~ tr{?XxNnBDHKMRSVWYbdhkmrsvwy}{N}; |
225
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# } |
226
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# else { |
227
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# $seq =~ s{[?XxNnBDHKMRSVWYbdhkmrsvwy]}{$char}xmsg; |
228
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# } |
229
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# } |
230
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231
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71
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2475
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$self->_set_seq($seq); |
232
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71
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430
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return $self; |
233
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} |
234
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235
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236
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sub spacify { |
237
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3069
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3069
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1
|
4808
|
my $self = shift; |
238
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239
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3069
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75319
|
my $seq = $self->seq; |
240
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241
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# uniformize runs of [*-space] having at least one 'true' space |
242
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# Note: we cannot use replace_seq because of the g flag |
243
|
3069
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|
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|
103260
|
$seq =~ s{ ( $GAP+ \ + ) }{ ' ' x length($1) }xmseg; |
|
550
|
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5655
|
|
244
|
3069
|
|
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|
79700
|
$seq =~ s{ ( \ + $GAP+ ) }{ ' ' x length($1) }xmseg; |
|
561
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5426
|
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245
|
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246
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|
|
# Note: two simpler regexes are muuuuuch faster than one complicated regex! |
247
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|
|
# $seq =~ s{ ( $GAP* \ + $GAP* ) }{ ' ' x length($1) }xmseg; |
248
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249
|
3069
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|
89705
|
$self->_set_seq($seq); |
250
|
3069
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|
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10557
|
return $self; |
251
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} |
252
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253
|
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254
|
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|
|
sub trim { |
255
|
3068
|
|
|
3068
|
1
|
5429
|
my $self = shift; |
256
|
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|
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|
257
|
3068
|
|
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|
110315
|
$self->replace_seq( qr{ $GAP+\z }xms, q{} ); |
258
|
3068
|
|
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|
|
12903
|
return $self; |
259
|
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|
} |
260
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261
|
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262
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|
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|
|
sub pad_to { |
263
|
3068
|
|
|
3068
|
1
|
4785
|
my $self = shift; |
264
|
3068
|
|
|
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|
4082
|
my $bound = shift; |
265
|
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|
266
|
3068
|
|
|
|
|
97954
|
$self->append_seq( q{ } x ($bound - $self->seq_len) ); |
267
|
3068
|
|
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|
|
9775
|
return $self; |
268
|
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|
|
} |
269
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|
270
|
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271
|
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|
|
|
sub clear_new_tag { |
272
|
3
|
|
|
3
|
1
|
6
|
my $self = shift; |
273
|
|
|
|
|
|
|
|
274
|
3
|
|
|
|
|
11
|
(my $full_id = $self->full_id) =~ s{$NEW_TAG\z}{}xms; |
275
|
3
|
|
|
|
|
88
|
$self->set_seq_id( SeqId->new( full_id => $full_id ) ); |
276
|
|
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|
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|
|
277
|
3
|
|
|
|
|
88
|
return $self; |
278
|
|
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|
|
|
} |
279
|
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|
|
|
280
|
|
|
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|
|
|
# site-wise methods (0-numbered) |
281
|
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|
|
282
|
|
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|
|
|
283
|
|
|
|
|
|
|
sub all_states { |
284
|
4203
|
|
|
4203
|
1
|
6205
|
my $self = shift; |
285
|
4203
|
|
|
|
|
108452
|
return split //, $self->seq; |
286
|
|
|
|
|
|
|
} |
287
|
|
|
|
|
|
|
|
288
|
|
|
|
|
|
|
|
289
|
|
|
|
|
|
|
sub state_at { ## no critic (RequireArgUnpacking) |
290
|
2002847
|
|
|
2002847
|
1
|
65348612
|
return shift->edit_seq(@_, 1); |
291
|
|
|
|
|
|
|
} |
292
|
|
|
|
|
|
|
|
293
|
|
|
|
|
|
|
|
294
|
|
|
|
|
|
|
sub delete_site { ## no critic (RequireArgUnpacking) |
295
|
0
|
|
|
0
|
1
|
0
|
my $self = shift; |
296
|
|
|
|
|
|
|
|
297
|
0
|
|
|
|
|
0
|
$self->edit_seq(@_, 1, q{}); |
298
|
0
|
|
|
|
|
0
|
return $self; |
299
|
|
|
|
|
|
|
} |
300
|
|
|
|
|
|
|
|
301
|
|
|
|
|
|
|
|
302
|
|
|
|
|
|
|
sub is_missing { |
303
|
40
|
|
|
40
|
1
|
156
|
my $self = shift; |
304
|
40
|
|
|
|
|
58
|
my $site = shift; |
305
|
|
|
|
|
|
|
|
306
|
40
|
|
|
|
|
98
|
my $state = $self->state_at($site); |
307
|
40
|
100
|
|
|
|
209
|
return 1 if $state =~ $PROTMISS; |
308
|
38
|
100
|
100
|
|
|
140
|
return 1 if $state =~ $DNAMISS && (not $self->is_protein); |
309
|
37
|
|
|
|
|
235
|
return 0; # X (or N depending on seq type) |
310
|
|
|
|
|
|
|
} |
311
|
|
|
|
|
|
|
|
312
|
|
|
|
|
|
|
|
313
|
|
|
|
|
|
|
sub is_gap { |
314
|
139
|
|
|
139
|
1
|
273
|
my $self = shift; |
315
|
139
|
|
|
|
|
176
|
my $site = shift; |
316
|
|
|
|
|
|
|
|
317
|
139
|
100
|
|
|
|
245
|
return 1 if $self->state_at($site) =~ $GAP; |
318
|
109
|
|
|
|
|
344
|
return 0; |
319
|
|
|
|
|
|
|
} |
320
|
|
|
|
|
|
|
|
321
|
|
|
|
|
|
|
|
322
|
|
|
|
|
|
|
# global methods |
323
|
|
|
|
|
|
|
|
324
|
|
|
|
|
|
|
around qw(purity reverse_complemented_seq codons) => sub { |
325
|
|
|
|
|
|
|
my $method = shift; |
326
|
|
|
|
|
|
|
my $self = shift; |
327
|
|
|
|
|
|
|
|
328
|
|
|
|
|
|
|
# Note: we return an explicit undef to emulate other accessor behavior |
329
|
|
|
|
|
|
|
if ($self->is_protein) { |
330
|
|
|
|
|
|
|
carp '[BMC] Warning: sequence looks like a protein; returning undef!'; |
331
|
|
|
|
|
|
|
return undef; ## no critic (ProhibitExplicitReturnUndef) |
332
|
|
|
|
|
|
|
} |
333
|
|
|
|
|
|
|
|
334
|
|
|
|
|
|
|
return $self->$method(@_); |
335
|
|
|
|
|
|
|
}; |
336
|
|
|
|
|
|
|
|
337
|
|
|
|
|
|
|
|
338
|
|
|
|
|
|
|
sub nomiss_seq_len { |
339
|
361
|
|
|
361
|
1
|
572
|
my $self = shift; |
340
|
|
|
|
|
|
|
|
341
|
361
|
100
|
|
|
|
655
|
my $regex = $self->is_protein ? $PROTMISS : $DNAMISS; |
342
|
361
|
|
|
|
|
789
|
(my $raw_str = $self->raw_str) =~ s/$regex//xmsg; |
343
|
|
|
|
|
|
|
# TODO: decide how to handle ambiguous nucleotides |
344
|
|
|
|
|
|
|
|
345
|
361
|
|
|
|
|
1134
|
return length $raw_str; |
346
|
|
|
|
|
|
|
} |
347
|
|
|
|
|
|
|
|
348
|
|
|
|
|
|
|
|
349
|
|
|
|
|
|
|
sub purity { |
350
|
|
|
|
|
|
|
my $self = shift; |
351
|
|
|
|
|
|
|
|
352
|
|
|
|
|
|
|
(my $pure_seq = $self->seq) =~ s/$NONPUREDNA//xmsg; |
353
|
|
|
|
|
|
|
my $purity = 1.0 * length($pure_seq) / $self->seq_len; |
354
|
|
|
|
|
|
|
|
355
|
|
|
|
|
|
|
return $purity; |
356
|
|
|
|
|
|
|
} |
357
|
|
|
|
|
|
|
|
358
|
|
|
|
|
|
|
|
359
|
|
|
|
|
|
|
sub reverse_complemented_seq { |
360
|
|
|
|
|
|
|
my $self = shift; |
361
|
|
|
|
|
|
|
|
362
|
|
|
|
|
|
|
# reverse complement and preserve case |
363
|
|
|
|
|
|
|
# Note: RNA always becomes DNA |
364
|
|
|
|
|
|
|
my $new_seq = scalar reverse $self->seq; |
365
|
|
|
|
|
|
|
$new_seq =~ tr/ATUGCYRSWKMBDHVN/TAACGRYSWMKVHDBN/; |
366
|
|
|
|
|
|
|
$new_seq =~ tr/atugcyrswkmbdhvn/taacgryswmkvhdbn/; |
367
|
|
|
|
|
|
|
|
368
|
|
|
|
|
|
|
return $self->new( seq_id => $self->full_id, seq => $new_seq ); |
369
|
|
|
|
|
|
|
} |
370
|
|
|
|
|
|
|
|
371
|
|
|
|
|
|
|
|
372
|
|
|
|
|
|
|
sub spliced_seq { |
373
|
1
|
|
|
1
|
1
|
8
|
my $self = shift; |
374
|
1
|
|
|
|
|
3
|
my $blocks = shift; |
375
|
|
|
|
|
|
|
|
376
|
1
|
|
|
|
|
2
|
my $new_seq; |
377
|
1
|
|
|
|
|
30
|
my $seq = $self->seq; |
378
|
1
|
|
|
|
|
4
|
for my $block ( @{$blocks} ) { |
|
1
|
|
|
|
|
3
|
|
379
|
8
|
|
|
|
|
12
|
my ($start, $end) = @{$block}; |
|
8
|
|
|
|
|
14
|
|
380
|
8
|
|
|
|
|
20
|
$new_seq .= substr $seq, $start - 1, $end - $start + 1; |
381
|
|
|
|
|
|
|
} |
382
|
|
|
|
|
|
|
|
383
|
1
|
|
|
|
|
9
|
return $self->new( seq_id => $self->full_id, seq => $new_seq ); |
384
|
|
|
|
|
|
|
} |
385
|
|
|
|
|
|
|
|
386
|
|
|
|
|
|
|
|
387
|
|
|
|
|
|
|
sub raw_str { |
388
|
518
|
|
|
518
|
1
|
860
|
my $self = shift; |
389
|
518
|
|
|
|
|
12901
|
return _strip_gaps($self->seq); |
390
|
|
|
|
|
|
|
} |
391
|
|
|
|
|
|
|
|
392
|
|
|
|
|
|
|
sub raw_seq { ## no critic (RequireArgUnpacking) |
393
|
0
|
|
|
0
|
0
|
0
|
carp '[BMC] Warning: Method raw_seq is deprecated; use raw_str instead!'; |
394
|
0
|
|
|
|
|
0
|
return shift->raw_str(@_); |
395
|
|
|
|
|
|
|
} |
396
|
|
|
|
|
|
|
|
397
|
|
|
|
|
|
|
|
398
|
|
|
|
|
|
|
sub wrapped_str { |
399
|
113
|
|
|
113
|
1
|
185
|
my $self = shift; |
400
|
113
|
|
50
|
|
|
597
|
my $chunk = shift // 60; |
401
|
|
|
|
|
|
|
|
402
|
113
|
50
|
|
|
|
259
|
my $nowrap = $chunk < 0 ? 1 : 0; |
403
|
113
|
|
|
|
|
3767
|
my $width = $self->seq_len; |
404
|
113
|
50
|
|
|
|
266
|
$chunk = $width if $nowrap; |
405
|
|
|
|
|
|
|
|
406
|
113
|
|
|
|
|
154
|
my $str; |
407
|
113
|
|
|
|
|
276
|
for (my $site = 0; $site < $width; $site += $chunk) { |
408
|
7533
|
|
|
|
|
245226
|
$str .= $self->edit_seq($site, $chunk) . "\n"; |
409
|
|
|
|
|
|
|
} |
410
|
|
|
|
|
|
|
|
411
|
113
|
|
|
|
|
474
|
return $str; |
412
|
|
|
|
|
|
|
} |
413
|
|
|
|
|
|
|
|
414
|
|
|
|
|
|
|
|
415
|
|
|
|
|
|
|
sub codons { |
416
|
|
|
|
|
|
|
my $self = shift; |
417
|
|
|
|
|
|
|
my $frame = shift // 1; # defaults to frame +1 |
418
|
|
|
|
|
|
|
|
419
|
|
|
|
|
|
|
# get specified DNA strand |
420
|
|
|
|
|
|
|
my $dna = $frame < 0 ? $self->reverse_complemented_seq->seq : $self->seq; |
421
|
|
|
|
|
|
|
$dna =~ tr/Uu/Tt/; # ensure DNA |
422
|
|
|
|
|
|
|
|
423
|
|
|
|
|
|
|
# split strand into codons beginning at specified frame |
424
|
|
|
|
|
|
|
# ... and discard incomplete codons |
425
|
|
|
|
|
|
|
my @codons; |
426
|
|
|
|
|
|
|
for (my $i = (abs $frame) - 1; $i < length $dna; $i += 3) { |
427
|
|
|
|
|
|
|
my $codon = substr $dna, $i, 3; |
428
|
|
|
|
|
|
|
push @codons, $codon if length $codon == 3; |
429
|
|
|
|
|
|
|
} |
430
|
|
|
|
|
|
|
|
431
|
|
|
|
|
|
|
return \@codons; |
432
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} |
433
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434
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435
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# private subs |
436
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437
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sub _strip_gaps { |
438
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554
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554
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1011
|
my $seq = shift; |
439
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440
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554
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3285
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$seq =~ s/$GAP+//xmsg; |
441
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554
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3886
|
return $seq; # strip all gaps |
442
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} |
443
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444
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__PACKAGE__->meta->make_immutable; |
445
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1; |
446
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447
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__END__ |
448
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449
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=pod |
450
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451
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=head1 NAME |
452
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453
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Bio::MUST::Core::Seq - Nucleotide or protein sequence |
454
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455
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=head1 VERSION |
456
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457
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version 0.212670 |
458
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459
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=head1 SYNOPSIS |
460
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461
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# TODO |
462
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463
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|
=head1 DESCRIPTION |
464
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465
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# TODO |
466
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467
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=head1 CONSTRUCTORS |
468
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469
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=head2 clone |
470
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471
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=head2 reverse_complemented_seq |
472
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473
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=head2 spliced_seq |
474
|
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475
|
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|
=head1 ACCESSORS |
476
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477
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=head2 all_states |
478
|
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479
|
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=head2 state_at |
480
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481
|
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|
=head2 delete_site |
482
|
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483
|
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|
=head1 PROPERTIES |
484
|
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|
485
|
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|
|
=head2 is_protein |
486
|
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|
487
|
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|
=head2 is_rna |
488
|
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489
|
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|
=head2 is_aligned |
490
|
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491
|
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|
=head2 is_subseq_of |
492
|
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493
|
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|
=head2 is_superseq_of |
494
|
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|
495
|
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|
|
=head2 first_site |
496
|
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|
497
|
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|
|
=head2 is_missing |
498
|
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|
499
|
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|
|
=head2 is_gap |
500
|
|
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|
|
501
|
|
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|
|
=head2 nomiss_seq_len |
502
|
|
|
|
|
|
|
|
503
|
|
|
|
|
|
|
=head2 purity |
504
|
|
|
|
|
|
|
|
505
|
|
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|
|
|
|
=head1 MUTATORS |
506
|
|
|
|
|
|
|
|
507
|
|
|
|
|
|
|
=head2 uc |
508
|
|
|
|
|
|
|
|
509
|
|
|
|
|
|
|
=head2 recode |
510
|
|
|
|
|
|
|
|
511
|
|
|
|
|
|
|
=head2 degap |
512
|
|
|
|
|
|
|
|
513
|
|
|
|
|
|
|
=head2 gapify |
514
|
|
|
|
|
|
|
|
515
|
|
|
|
|
|
|
=head2 spacify |
516
|
|
|
|
|
|
|
|
517
|
|
|
|
|
|
|
=head2 trim |
518
|
|
|
|
|
|
|
|
519
|
|
|
|
|
|
|
=head2 pad_to |
520
|
|
|
|
|
|
|
|
521
|
|
|
|
|
|
|
=head2 clear_new_tag |
522
|
|
|
|
|
|
|
|
523
|
|
|
|
|
|
|
=head1 MISC METHODS |
524
|
|
|
|
|
|
|
|
525
|
|
|
|
|
|
|
=head2 raw_str |
526
|
|
|
|
|
|
|
|
527
|
|
|
|
|
|
|
=head2 wrapped_str |
528
|
|
|
|
|
|
|
|
529
|
|
|
|
|
|
|
=head2 codons |
530
|
|
|
|
|
|
|
|
531
|
|
|
|
|
|
|
=head1 AUTHOR |
532
|
|
|
|
|
|
|
|
533
|
|
|
|
|
|
|
Denis BAURAIN <denis.baurain@uliege.be> |
534
|
|
|
|
|
|
|
|
535
|
|
|
|
|
|
|
=head1 CONTRIBUTORS |
536
|
|
|
|
|
|
|
|
537
|
|
|
|
|
|
|
=for stopwords Catherine COLSON Arnaud DI FRANCO Valerian LUPO |
538
|
|
|
|
|
|
|
|
539
|
|
|
|
|
|
|
=over 4 |
540
|
|
|
|
|
|
|
|
541
|
|
|
|
|
|
|
=item * |
542
|
|
|
|
|
|
|
|
543
|
|
|
|
|
|
|
Catherine COLSON <ccolson@doct.uliege.be> |
544
|
|
|
|
|
|
|
|
545
|
|
|
|
|
|
|
=item * |
546
|
|
|
|
|
|
|
|
547
|
|
|
|
|
|
|
Arnaud DI FRANCO <arnaud.difranco@gmail.com> |
548
|
|
|
|
|
|
|
|
549
|
|
|
|
|
|
|
=item * |
550
|
|
|
|
|
|
|
|
551
|
|
|
|
|
|
|
Valerian LUPO <valerian.lupo@doct.uliege.be> |
552
|
|
|
|
|
|
|
|
553
|
|
|
|
|
|
|
=back |
554
|
|
|
|
|
|
|
|
555
|
|
|
|
|
|
|
=head1 COPYRIGHT AND LICENSE |
556
|
|
|
|
|
|
|
|
557
|
|
|
|
|
|
|
This software is copyright (c) 2013 by University of Liege / Unit of Eukaryotic Phylogenomics / Denis BAURAIN. |
558
|
|
|
|
|
|
|
|
559
|
|
|
|
|
|
|
This is free software; you can redistribute it and/or modify it under |
560
|
|
|
|
|
|
|
the same terms as the Perl 5 programming language system itself. |
561
|
|
|
|
|
|
|
|
562
|
|
|
|
|
|
|
=cut |