# $Id: TypeMapper.pm 16123 2009-09-17 12:57:27Z cjfields $ # # bioperl module for Bio::SeqFeature::Tools::TypeMapper # # Please direct questions and support issues to # # Cared for by Chris Mungall # # Copyright Chris Mungall # # You may distribute this module under the same terms as perl itself # POD documentation - main docs before the code =head1 NAME Bio::SeqFeature::Tools::TypeMapper - maps $seq_feature-Eprimary_tag =head1 SYNOPSIS use Bio::SeqIO; use Bio::SeqFeature::Tools::TypeMapper; # first fetch a genbank SeqI object $seqio = Bio::SeqIO->new(-file=>'AE003644.gbk', -format=>'GenBank'); $seq = $seqio->next_seq(); $tm = Bio::SeqFeature::Tools::TypeMapper->new; # map all the types in the sequence $tm->map_types(-seq=>$seq, {CDS=>'ORF', variation=>sub { my $f = shift; $f->length > 1 ? 'variation' : 'SNP' }, }); # alternatively, use the hardcoded SO mapping $tm->map_types_to_SO(-seq=>$seq); =head1 DESCRIPTION This class implements an object for mapping between types; for example, the types in a genbank feature table, and the types specified in the Sequence Ontology. You can specify your own mapping, either as a simple hash index, or by providing your own subroutines. =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 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 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: http://bugzilla.open-bio.org/ =head1 AUTHOR - Chris Mungall Email: cjm@fruitfly.org =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::SeqFeature::Tools::TypeMapper; use strict; # Object preamble - inherits from Bio::Root::Root use base qw(Bio::Root::Root); =head2 new Title : new Usage : $unflattener = Bio::SeqFeature::Tools::TypeMapper->new(); Function: constructor Example : Returns : a new Bio::SeqFeature::Tools::TypeMapper Args : see below =cut sub new { my($class,@args) = @_; my $self = $class->SUPER::new(@args); my($typemap) = $self->_rearrange([qw(TYPEMAP )], @args); $typemap && $self->typemap($typemap); return $self; # success - we hope! } =head2 typemap Title : typemap Usage : $obj->typemap($newval) Function: Example : Returns : value of typemap (a scalar) Args : on set, new value (a scalar or undef, optional) =cut sub typemap{ my $self = shift; return $self->{'typemap'} = shift if @_; return $self->{'typemap'}; } =head2 map_types Title : map_types Usage : Function: Example : Returns : Args : dgg: added -undefined => "region" option to produce all valid SO mappings. =cut sub map_types{ my ($self,@args) = @_; my($sf, $seq, $type_map, $undefmap) = $self->_rearrange([qw(FEATURE SEQ TYPE_MAP UNDEFINED )], @args); if (!$sf && !$seq) { $self->throw("you need to pass in either -feature or -seq"); } my @sfs = ($sf); if ($seq) { $seq->isa("Bio::SeqI") || $self->throw("$seq NOT A SeqI"); @sfs = $seq->get_all_SeqFeatures; } $type_map = $type_map || $self->typemap; # dgg: was type_map; foreach my $sf (@sfs) { $sf->isa("Bio::SeqFeatureI") || $self->throw("$sf NOT A SeqFeatureI"); $sf->isa("Bio::FeatureHolderI") || $self->throw("$sf NOT A FeatureHolderI"); my $type = $sf->primary_tag; my $mtype = $type_map->{$type}; if ($mtype) { if (ref($mtype)) { if (ref($mtype) eq 'CODE') { $mtype = $mtype->($sf); } else { $self->throw('must be scalar or CODE ref'); } } elsif ($undefmap && $mtype eq 'undefined') { # dgg $mtype= $undefmap; } $sf->primary_tag($mtype); } } return; } =head2 map_types_to_SO Title : map_types_to_SO Usage : Function: Example : Returns : Args : hardcodes the genbank to SO mapping Based on revision 1.22 of SO Please see the actual code for the mappings Taken from L dgg: separated out FT_SO_map for caller changes. Update with: open(FTSO,"curl -s http://sequenceontology.org/resources/mapping/FT_SO.txt|"); while(){ chomp; ($ft,$so,$sid,$ftdef,$sodef)= split"\t"; print " '$ft' => '$so',\n" if($ft && $so && $ftdef); } =cut sub FT_SO_map { # $self= shift; # note : some of the FT_SO mappings are commented out and overriden... return { "FT term" => "SO term", "-" => "located_sequence_feature", "-10_signal" => "minus_10_signal", "-35_signal" => "minus_35_signal", "3'UTR" => "three_prime_UTR", "3'clip" => "three_prime_clip", "5'UTR" => "five_prime_UTR", "5'clip" => "five_prime_clip", "CAAT_signal" => "CAAT_signal", "CDS" => "CDS", "C_region" => "undefined", "D-loop" => "D_loop", "D_segment" => "D_gene", "GC_signal" => "GC_rich_region", "J_segment" => "undefined", "LTR" => "long_terminal_repeat", "N_region" => "undefined", "RBS" => "ribosome_entry_site", "STS" => "STS", "S_region" => "undefined", "TATA_signal" => "TATA_box", "V_region" => "undefined", "V_segment" => "undefined", "attenuator" => "attenuator", "conflict" => "undefined", "enhancer" => "enhancer", "exon" => "exon", "gap" => "gap", "gene" => "gene", "iDNA" => "iDNA", "intron" => "intron", "mRNA" => "mRNA", "mat_peptide" => "mature_protein_region", "mature_peptide" => "mature_protein_region", # "misc_RNA" => "transcript", "misc_binding" => "binding_site", "misc_difference" => "sequence_difference", "misc_feature" => "region", "misc_recomb" => "recombination_feature", "misc_signal" => "regulatory_region", "misc_structure" => "sequence_secondary_structure", "modified_base" => "modified_base_site", "old_sequence" => "undefined", "operon" => "operon", "oriT" => "origin_of_transfer", "polyA_signal" => "polyA_signal_sequence", "polyA_site" => "polyA_site", "precursor_RNA" => "primary_transcript", "prim_transcript" => "primary_transcript", "primer_bind" => "primer_binding_site", "promoter" => "promoter", "protein_bind" => "protein_binding_site", "rRNA" => "rRNA", "repeat_region" => "repeat_region", "repeat_unit" => "repeat_unit", "satellite" => "satellite_DNA", "scRNA" => "scRNA", "sig_peptide" => "signal_peptide", "snRNA" => "snRNA", "snoRNA" => "snoRNA", # "source" => "databank_entry", "stem_loop" => "stem_loop", "tRNA" => "tRNA", "terminator" => "terminator", "transit_peptide" => "transit_peptide", "unsure" => "undefined", "variation" => "sequence_variant", "pseudomRNA" => "pseudogenic_transcript", ## has parent = pseudogene ; dgg "pseudotranscript" => "pseudogenic_transcript", ## from Unflattener misc_RNA ; dgg "pseudoexon" => "pseudogenic_exon", "pseudoCDS" => "pseudogenic_exon", "pseudomisc_feature" => "pseudogenic_region", "pseudointron" => "pseudogenic_region", ## "undefined" => "region", # this is the most generic form for RNAs; # we always represent the processed form of # the transcript misc_RNA=>'processed_transcript', # not sure about this one... source=>'contig', rep_origin=>'origin_of_replication', Protein=>'protein', }; } sub map_types_to_SO{ my ($self,@args) = @_; push(@args, (-type_map=> $self->FT_SO_map() ) ); return $self->map_types(@args); } =head2 get_relationship_type_by_parent_child Title : get_relationship_type_by_parent_child Usage : $type = $tm->get_relationship_type_by_parent_child($parent_sf, $child_sf); Usage : $type = $tm->get_relationship_type_by_parent_child('mRNA', 'protein'); Function: given two features where the parent contains the child, will determine what the relationship between them in Example : Returns : Args : parent SeqFeature, child SeqFeature OR parent type string, child type string OR bioperl Seq::FeatureHolderI hierarchies are equivalent to unlabeled graphs (where parent nodes are the containers, and child nodes are the features being contained). For example, a feature of type mRNA can contain features of type exon. Some external representations (eg chadoxml or chaosxml) require that the edges in the feature relationship graph are labeled. For example, the type between mRNA and exon would be B. Although it stretches the bioperl notion of containment, we could have a CDS contained by an mRNA (for example, the L module takes genbank records and makes these kind of links. The relationship here would be B In chado speak, the child is the B feature and the parent is the B feature =cut sub get_relationship_type_by_parent_child { my ($self,$parent,$child) = @_; $parent = ref($parent) ? $parent->primary_tag : $parent; $child = ref($child) ? $child->primary_tag : $child; my $type = 'part_of'; # default # TODO - do this with metadata, or infer via SO itself if (lc($child) eq 'protein') { $type = 'derives_from'; } if (lc($child) eq 'polypeptide') { $type = 'derives_from'; } return $type; } 1;