———————————=head1 NAME
Bio::Matrix::PSM::InstanceSite - A PSM site occurrence
=head1 SYNOPSIS
use Bio::Matrix::PSM::InstanceSite;
#You can get an InstanceSite object either from a file:
my ($instances,$matrix)=$SomePSMFile->parse_next;
#or from memory
my %params=(seq=>'TATAAT',
id=>"TATAbox1", accession=>'ENSG00000122304', mid=>'TB1',
desc=>'TATA box, experimentally verified in PRM1 gene',
-relpos=>-35, -anchor=>'CHR7', -start=>35000921, -end=>35000926);
#Last 2 arguments are passed to create a Bio::LocatableSeq object
#Anchor shows the coordinates system for the Bio::LocatableSeq object
=head1 DESCRIPTION
Abstract interface to PSM site occurrence (PSM sequence
match). InstanceSite objects may be used to describe a PSM (See
L<Bio::Matrix::PSM::SiteMatrix>) sequence matches. The usual
characteristic of such a match is sequence coordinates, score,
sequence and sequence (gene) identifier- accession number or other id.
This object inherits from Bio::LocatableSeq (which defines the real
sequence) and might hold a SiteMatrix object, used to detect the CRE
(cis-regulatory element), or created from this CRE.
While the documentation states that the motif id and gene id
(accession) combination should be unique, this is not entirely true-
there might be more than one occurrence of the same cis-regulatory
element in the upstream region of the same gene. Therefore relpos
would be the third element to create a really unique combination.
=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 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
=head2 Support
Please direct usage questions or support issues to the mailing list:
I<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.
=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:
=head2 Description
Bio::Matrix::PSM::InstanceSiteI implementation
=head1 AUTHOR - Stefan Kirov
Email skirov@utk.edu
=head1 APPENDIX
=cut
# Let the code begin...
package
Bio::Matrix::PSM::InstanceSite;
$Bio::Matrix::PSM::InstanceSite::VERSION
=
'1.7.8'
;
use
strict;
=head2 new
Title : new
Usage : my $isntance=Bio::Matrix::PSM::InstanceSite->new
(-seq=>'TATAAT', -id=>"TATAbox1",
-accession_number='ENSG00000122304', -mid=>'TB1',
-desc=>'TATA box, experimentally verified in PRM1 gene',
-relpos=>-35, -anchor=>'CHR7', -start=>35000921, -end=>35000926, strand=>1)
Function: Creates an InstanceSite object from memory.
Throws :
Example :
Returns : Bio::Matrix::PSM::InstanceSite object
Args : hash
=cut
sub
new {
my
(
$class
,
@args
) =
@_
;
my
%args
=
@args
;
#Too many things to rearrange, and I am creating >1K such objects routinely, so this is a performance issue
$args
{
'-start'
} ||= 1;
my
$end
=
$args
{
'-start'
} +
length
(
$args
{-seq}) -1;
if
(!
defined
(
$args
{-strand})) {
$args
{-strand}=1;
@args
=
%args
;
}
my
$self
=
$class
->SUPER::new(
@args
,
'-end'
,
$end
);
while
(
@args
) {
(
my
$key
=
shift
@args
) =~ s/-//gi;
#deletes all dashes (only dashes)!
$args
{
$key
} =
shift
@args
;
}
#should throw exception if seq is null, for now just warn
if
((
$args
{seq} eq
''
) || (!
defined
(
$args
{seq}))) {
$args
{seq}=
"AGCT"
;
warn
"No sequence?!\n"
;
}
$self
->{mid}=
$args
{mid};
$self
->seq(
$args
{seq});
$self
->desc(
$args
{desc});
$self
->{score}=
$args
{score};
$self
->{relpos}=
$args
{relpos};
$self
->{frame}=
$args
{frame};
$self
->{anchor}=
$args
{anchor};
return
$self
;
}
=head2 mid
Title : mid
Usage : my $mid=$instance->mid;
Function: Get/Set the motif id
Throws :
Example :
Returns : scalar
Args : scalar
=cut
sub
mid {
my
$self
=
shift
;
my
$prev
=
$self
->{mid};
if
(
@_
) {
$self
->{mid} =
shift
; }
return
$prev
;
}
=head2 score
Title : score
Usage : my $score=$instance->score;
Function: Get/Set the score (mismatches) between the instance and the attached (or
initial) PSM
Throws :
Example :
Returns : real number
Args : real number
=cut
sub
score {
my
$self
=
shift
;
my
$prev
=
$self
->{score};
if
(
@_
) {
$self
->{score} =
shift
; }
return
$prev
;
}
=head2 anchor
Title : anchor
Usage : my $anchor=$instance->anchor;
Function: Get/Set the anchor which shows what coordinate system start/end use
Throws :
Example :
Returns : string
Args : string
=cut
sub
anchor {
my
$self
=
shift
;
my
$prev
=
$self
->{anchor};
if
(
@_
) {
$self
->{anchor} =
shift
; }
return
$prev
;
}
=head2 start
Title : start
Usage : my $start=$instance->start;
Function: Get/Set the position of the instance on the sequence used
Throws :
Example :
Returns : integer
Args : integer
=cut
#Provided by LocatableSeq
=head2 minstance
Title : minstance
Usage : my $minstance=$misntance->score;
Function: Get/Set the unique identifier- sequence id/motif id, for example PRM1_TATAbox.
Not necessarily human readable.
Throws :
Example :
Returns : string
Args : string
=cut
sub
minstance {
my
$self
=
shift
;
my
$prev
=
$self
->{minstance};
if
(
@_
) {
$self
->{minstance} =
shift
; }
return
$prev
;
}
=head2 relpos
Title : relpos
Usage : my $seqpos=$instance->relpos;
Function: Get/Set the relative position of the instance with respect to the transcription start
site (if known). Can and usually is negative.
Throws :
Example :
Returns : integer
Args : integer
=cut
sub
relpos {
my
$self
=
shift
;
my
$prev
=
$self
->{relpos};
if
(
@_
) {
$self
->{relpos} =
shift
; }
return
$prev
;
}
=head2 annotation
Title : annotation
Usage : $ann = $seq->annotation or $seq->annotation($annotation)
Function: Gets or sets the annotation
Returns : L<Bio::AnnotationCollectionI> object
Args : None or L<Bio::AnnotationCollectionI> object
See L<Bio::AnnotationCollectionI> and L<Bio::Annotation::Collection>
for more information
=cut
sub
annotation {
my
(
$obj
,
$value
) =
@_
;
if
(
defined
$value
) {
$obj
->throw(
"object of class "
.
ref
(
$value
).
" does not implement "
.
"Bio::AnnotationCollectionI. Too bad."
)
unless
$value
->isa(
"Bio::AnnotationCollectionI"
);
$obj
->{
'_annotation'
} =
$value
;
}
elsif
( !
defined
$obj
->{
'_annotation'
}) {
$obj
->{
'_annotation'
} = Bio::Annotation::Collection->new();
}
return
$obj
->{
'_annotation'
};
}
=head2 species
Title : species
Usage : $species = $seq->species() or $seq->species($species)
Function: Gets or sets the species
Returns : L<Bio::Species> object
Args : None or L<Bio::Species> object
See L<Bio::Species> for more information
=cut
sub
species {
my
(
$self
,
$species
) =
@_
;
if
(
$species
) {
$self
->{
'species'
} =
$species
;
}
else
{
return
$self
->{
'species'
};
}
}
=head2 frame
Title : frame
Usage : my $frane=$instance->frame;
Function: Get/Set the frame of a DNA instance with respect to a protein motif used.
Returns undef if the motif was not protein or the DB is protein.
Throws :
Example :
Returns : integer
Args : integer (0, 1, 2)
=cut
sub
frame {
my
$self
=
shift
;
my
$prev
=
$self
->{frame};
if
(
@_
) {
$self
->{frame} =
shift
;
$self
->throw(
"This is not a legitimate frame"
)
unless
(
grep
(/
$self
->{frame}/,
qw[0 1 2]
)); }
return
$prev
;
}
1;