Provided by: libbio-perl-perl_1.6.923-1_all bug

NAME

       Bio::Tools::Analysis::Protein::Domcut -  a wrapper around Domcut server

SYNOPSIS

         use   Bio::Tools::Analysis::Protein::Domcut;
         #get a  Bio::PrimarySeq
         use Bio::PrimarySeq;
         my $seq = Bio::PrimarySeq->new
            (-seq=>'IKLCVNLAILAKAHLIELALAL',
            -primary_id=>'test'); # a Bio::PrimarySeqI object

         my $domcut = Bio::Tools::Analysis::Protein::Domcut->new (-seq=>$seq);
         $domcut->run;
         print $domcut->result;# #raw text to standard out

DESCRIPTION

       A module to remotely retrieve predictions of protein domain boundaries.  Each residue in the protein
       receives a score, those better than the significance threshold and at a local minimum receive a rank -
       i.e., the best minimum is rank 1, the second best minimum is rank2 etc. These correspond to domain
       boundaries.  e.g.,

         my $analysis_object = Bio::Tools::Analysis::Protein::Domcut->new
            (-seq => $seq);

       creates a new object. The sequence supplied must be a Bio::PrimarySeq and not a Bio::Seq object.

         $analysis_object->run;

       submits the query to the server and obtains raw text output

       Given an amino acid sequence the results can be obtained in 4 formats, determined by the argument to the
       result method

       1.  The raw text of the program output

             my $rawdata = $analysis_object->result;

       2.  A  reference  to  an array of hashes of scores for each state and the assigned state. Each element in
           the array is a residue (indexed from 0).

             my $data_ref = $analysis_object->result('parsed');
             print "score for helix at residue 2 is $data_ref->[1]{'helix'}\n";
             print "predicted struc  at residue 2 is $data_ref->[1]{'struc}\n";

       3.  An array of Bio::SeqFeature::Generic objects where each feature is  a  predicted  unit  of  secondary
           structure.  Only  stretches  of  helix/sheet  predictions  for  longer than 4 residues are defined as
           helices.  So, in order to add features to an existing Bio::Seq object;

             # get a Bio::Seq object
             my $seqobj;
             my $tool = Bio::Tools::Analysis::Protein::Domcut->new
                 ( -seq => $seqobj->primary_seq);
             $tool->run;

             my @fts = $tool->result(Bio::SeqFeatureI);

             $seqobj->add_SeqFeature(@fts);

             # if you want  meta sequences as well :
             my $meta = $tool->result('meta');
             $seqobj->primary_seq($meta);

             # can access meta data in a Bio::Seq object via a
             # call to primary_seq:

             print $seq4->primary_seq->named_submeta_text('Domcut', 1,2), "\n";

       4.  A Bio::Seq::Meta::Array implementing sequence.

           This is a Bio::Seq object that can also hold data about each residue in the sequence. In  this  case,
           the sequence can be associated with a single array of Domcut prediction scores.  e.g.,

             my $meta_sequence = $analysis_object->result('meta');
             print "scores from residues 10 -20 are ",
                 $meta_sequence->submeta_text(10,20), "\n";

           Many methods common to all analyses are inherited from Bio::Tools::Analysis::SimpleAnalysisBase.

SEE ALSO

       Bio::SimpleAnalysisI, Bio::Tools::Analysis::SimpleAnalysisBase, Bio::Seq::Meta::Array, Bio::WebAgent

FEEDBACK

   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

   Support
       Please direct usage questions or support issues to the mailing list:

       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.

   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/

AUTHORS

       Richard Adams, Richard.Adams@ed.ac.uk,

APPENDIX

       The rest of the documentation details each of the object methods. Internal methods are  usually  preceded
       with a _

   result
        Name    : result
        Purpose : To retrieve results of analysis in one of several formats.
        Usage   : $job->result (...)
        Returns : a result created by running an analysis
        Args    : various - see keysin $RESULT_SPEC.

       The  method  returns  a  result  of an executed job. If the job was terminated by an error the result may
       contain an error message instead of the real data.

       This implementation returns differently processed data depending on argument:

       undef
          Returns the raw ASCII data stream but without HTML tags

       'Bio::SeqFeatureI'
          The argument string defines the type of bioperl  objects  returned  in  an  array.   The  objects  are
          Bio::SeqFeature::Generic. Tagnames are 'score' and 'rank'.

       'parsed'
          Array of array references of [score, rank].

       'all'
          A  Bio::Seq::Meta::Array  object.  Scores can be accessed using methods from this class. Meta sequence
          name is Domcut.

perl v5.18.2                                       2014-01-18              Bio::Tools::An...Protein::Domcut(3pm)