table of contents
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,"\t", sprintf("%.1f", $bands{$band}),"\n"; } #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://github.com/bioperl/bioperl-live/issues
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
2018-10-27 | perl v5.26.2 |