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Bio::Tools::Gel(3pm)					User Contributed Perl Documentation				      Bio::Tools::Gel(3pm)

NAME
Bio::Tools::Gel - Calculates relative electrophoretic migration distances SYNOPSIS
use Bio::PrimarySeq; use Bio::Restriction::Analysis; use Bio::Tools::Gel; # get a sequence my $d = 'AAAAAAAAAGAATTCTTTTTTTTTTTTTTGAATTCGGGGGGGGGGGGGGGGGGGG'; my $seq1 = Bio::Seq->new(-id=>'groundhog day',-seq=>$d); # cut it with an enzyme my $ra=Bio::Restriction::Analysis->new(-seq=>$seq1); @cuts = $ra->fragments('EcoRI'), 3; # analyse the fragments in a gel my $gel = Bio::Tools::Gel->new(-seq=>@cuts,-dilate=>10); my %bands = $gel->bands; foreach my $band (sort {$b <=> $a} keys %bands){ print $band," ", sprintf("%.1f", $bands{$band})," "; } #prints: #20 27.0 #25 26.0 #10 30.0 DESCRIPTION
This takes a set of sequences or Bio::Seq objects, and calculates their respective migration distances using: distance = dilation * (4 - log10(length(dna)); Source: Molecular Cloning, a Laboratory Manual. Sambrook, Fritsch, Maniatis. CSHL Press, 1989. Bio::Tools::Gel currently calculates migration distances based solely on the length of the nucleotide sequence. Secondary or tertiary structure, curvature, and other biophysical attributes of a sequence are currently not considered. Polypeptide migration is currently not supported. 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 the Bioperl mailing list. 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 of the bugs and their resolution. Bug reports can be submitted via the web: https://redmine.open-bio.org/projects/bioperl/ AUTHOR - Allen Day Email allenday@ucla.edu APPENDIX
The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _ new Title : new Usage : my $gel = Bio::Tools::Gel->new(-seq => $sequence,-dilate => 3); Function: Initializes a new Gel Returns : Bio::Tools::Gel Args : -seq => Bio::Seq(s), scalar(s) or list of either/both (default: none) -dilate => Expand band migration distances (default: 1) add_band Title : add_band Usage : $gel->add_band($seq); Function: Calls _add_band with a (possibly created) Bio::Seq object. Returns : Args : Bio::Seq, scalar sequence, or list of either/both. _add_band Title : _add_band Usage : $gel->_add_band($seq); Function: Adds a new band to the gel. Returns : Args : Bio::Seq object dilate Title : dilate Usage : $gel->dilate(1); Function: Sets/retrieves the dilation factor. Returns : dilation factor Args : Float or none bands Title : bands Usage : $gel->bands; Function: Calculates migration distances of sequences. Returns : hash of (seq_id => distance) Args : log10 Title : log10 Usage : log10($n); Function: returns base 10 log of $n. Returns : float Args : float perl v5.14.2 2012-03-02 Bio::Tools::Gel(3pm)

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Bio::Seq::SeqFactory(3pm)				User Contributed Perl Documentation				 Bio::Seq::SeqFactory(3pm)

NAME
Bio::Seq::SeqFactory - Instantiates a new Bio::PrimarySeqI (or derived class) through a factory SYNOPSIS
use Bio::Seq::SeqFactory; my $factory = Bio::Seq::SeqFactory->new(); my $seq = $factory->create(-seq => 'WYRAVLC', -id => 'name'); # If you want the factory to create Bio::Seq objects instead # of the default Bio::PrimarySeq objects, use the -type parameter: my $factory = Bio::Seq::SeqFactory->new(-type => 'Bio::Seq'); DESCRIPTION
This object will build Bio::PrimarySeqI and Bio::SeqI objects generically. 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 the Bioperl mailing list. 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 of the bugs and their resolution. Bug reports can be submitted via the web: https://redmine.open-bio.org/projects/bioperl/ AUTHOR - Jason Stajich Email jason@bioperl.org APPENDIX
The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _ new Title : new Usage : my $obj = Bio::Seq::SeqFactory->new(); Function: Builds a new Bio::Seq::SeqFactory object Returns : Bio::Seq::SeqFactory Args : -type => string, name of a PrimarySeqI derived class This is optional. Default=Bio::PrimarySeq. create Title : create Usage : my $seq = $seqbuilder->create(-seq => 'CAGT', -id => 'name'); Function: Instantiates new Bio::SeqI (or one of its child classes) This object allows us to genericize the instantiation of sequence objects. Returns : Bio::PrimarySeq object (default) The return type is configurable using new(-type =>"..."). Args : initialization parameters specific to the type of sequence object we want. Typically -seq => $str, -display_id => $name type Title : type Usage : $obj->type($newval) Function: Returns : value of type Args : newvalue (optional) perl v5.14.2 2012-03-02 Bio::Seq::SeqFactory(3pm)
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