NAME
FAST::Bio::Search::SearchUtils - Utility functions for FAST::Bio::Search:: objects
SYNOPSIS
# This module is just a collection of subroutines, not an object.DESCRIPTION
The SearchUtils.pm module is a collection of subroutines used primarily by FAST::Bio::Search::Hit::HitI objects for some of the additional functionality, such as HSP tiling. Right now, the SearchUtils is just a collection of methods, not an object.
AUTHOR
Steve Chervitz <sac@bioperl.org>
CONTRIBUTORS
Sendu Bala, bix@sendu.me.uk
tile_hsps
Usage : tile_hsps( $sbjct );
: This is called automatically by methods in FAST::Bio::Search::Hit::GenericHit
: that rely on having tiled data.
:
: If you are interested in getting data about the constructed HSP contigs:
: my ($qcontigs, $scontigs) = FAST::Bio::Search::SearchUtils::tile_hsps($hit);
: if (ref $qcontigs) {
: print STDERR "Query contigs:\n";
: foreach (@{$qcontigs}) {
: print "contig start is $_->{'start'}\n";
: print "contig stop is $_->{'stop'}\n";
: }
: }
: See below for more information about the contig data structure.
:
Purpose : Collect statistics about the aligned sequences in a set of HSPs.
: Calculates the following data across all HSPs:
: -- total alignment length
: -- total identical residues
: -- total conserved residues
Returns : If there was only a single HSP (so no tiling was necessary)
tile_hsps() returns a list of two non-zero integers.
If there were multiple HSP,
tile_hsps() returns a list of two array references containin HSP contig data.
The first array ref contains a list of HSP contigs on the query sequence.
The second array ref contains a list of HSP contigs on the subject sequence.
Each contig is a hash reference with the following data fields:
'start' => start coordinate of the contig
'stop' => start coordinate of the contig
'iden' => number of identical residues in the contig
'cons' => number of conserved residues in the contig
'strand'=> strand of the contig
'frame' => frame of the contig
Argument : A FAST::Bio::Search::Hit::HitI object
Throws : n/a
Comments :
: This method performs more careful summing of data across
: all HSPs in the Sbjct object. Only HSPs that are in the same strand
: and frame are tiled. Simply summing the data from all HSPs
: in the same strand and frame will overestimate the actual
: length of the alignment if there is overlap between different HSPs
: (often the case).
:
: The strategy is to tile the HSPs and sum over the
: contigs, collecting data separately from overlapping and
: non-overlapping regions of each HSP. To facilitate this, the
: HSP.pm object now permits extraction of data from sub-sections
: of an HSP.
:
: Additional useful information is collected from the results
: of the tiling. It is possible that sub-sequences in
: different HSPs will overlap significantly. In this case, it
: is impossible to create a single unambiguous alignment by
: concatenating the HSPs. The ambiguity may indicate the
: presence of multiple, similar domains in one or both of the
: aligned sequences. This ambiguity is recorded using the
: ambiguous_aln() method.
:
: This method does not attempt to discern biologically
: significant vs. insignificant overlaps. The allowable amount of
: overlap can be set with the overlap() method or with the -OVERLAP
: parameter used when constructing the Hit object.
:
: For a given hit, both the query and the sbjct sequences are
: tiled independently.
:
: -- If only query sequence HSPs overlap,
: this may suggest multiple domains in the sbjct.
: -- If only sbjct sequence HSPs overlap,
: this may suggest multiple domains in the query.
: -- If both query & sbjct sequence HSPs overlap,
: this suggests multiple domains in both.
: -- If neither query & sbjct sequence HSPs overlap,
: this suggests either no multiple domains in either
: sequence OR that both sequences have the same
: distribution of multiple similar domains.
:
: This method can deal with the special case of when multiple
: HSPs exactly overlap.
:
: Efficiency concerns:
: Speed will be an issue for sequences with numerous HSPs.
:
Bugs : Currently, tile_hsps() does not properly account for
: the number of non-tiled but overlapping HSPs, which becomes a problem
: as overlap() grows. Large values overlap() may thus lead to
: incorrect statistics for some hits. For best results, keep overlap()
: below 5 (DEFAULT IS 2). For more about this, see the "HSP Tiling and
: Ambiguous Alignments" section in L<FAST::Bio::Search::Hit::GenericHit>.See Also : _adjust_contigs(), FAST::Bio::Search::Hit::GenericHit
logical_length
Usage : logical_length( $alg_name, $seq_type, $length );
Purpose : Determine the logical length of an aligned sequence based on
: algorithm name and sequence type.
Returns : integer representing the logical aligned length.
Argument : $alg_name = name of algorigthm (e.g., blastx, tblastn)
: $seq_type = type of sequence (e.g., query or hit)
: $length = physical length of the sequence in the alignment.
Throws : n/a
Comments : This function is used to account for the fact that number of identities
and conserved residues is reported in peptide space while the query
length (in the case of BLASTX and TBLASTX) and/or the hit length
(in the case of TBLASTN and TBLASTX) are in nucleotide space.
The adjustment affects the values reported by the various frac_XXX
methods in GenericHit and GenericHSP.get_exponent
Usage : &get_exponent( number );
Purpose : Determines the power of 10 exponent of an integer, float,
: or scientific notation number.
Example : &get_exponent("4.0e-206");
: &get_exponent("0.00032");
: &get_exponent("10.");
: &get_exponent("1000.0");
: &get_exponent("e+83");
Argument : Float, Integer, or scientific notation number
Returns : Integer representing the exponent part of the number (+ or -).
: If argument == 0 (zero), return value is "-999".
Comments : Exponents are rounded up (less negative) if the mantissa is >= 5.
: Exponents are rounded down (more negative) if the mantissa is <= -5.collapse_nums
Usage : @cnums = collapse_nums( @numbers );
Purpose : Collapses a list of numbers into a set of ranges of consecutive terms:
: Useful for condensing long lists of consecutive numbers.
: EXPANDED:
: 1 2 3 4 5 6 10 12 13 14 15 17 18 20 21 22 24 26 30 31 32
: COLLAPSED:
: 1-6 10 12-15 17 18 20-22 24 26 30-32
Argument : List of numbers sorted numerically.
Returns : List of numbers mixed with ranges of numbers (see above).
Throws : n/aSee Also : FAST::Bio::Search::Hit::BlastHit::seq_inds()
strip_blast_html
Usage : $boolean = &strip_blast_html( string_ref );
: This method is exported.
Purpose : Removes HTML formatting from a supplied string.
: Attempts to restore the Blast report to enable
: parsing by FAST::Bio::SearchIO::blast.pm
Returns : Boolean: true if string was stripped, false if not.
Argument : string_ref = reference to a string containing the whole Blast
: report containing HTML formatting.
Throws : Croaks if the argument is not a scalar reference.
Comments : Based on code originally written by Alex Dong Li
: (ali@genet.sickkids.on.ca).
: This method does some Blast-specific stripping
: (adds back a '>' character in front of each HSP
: alignment listing).
:
: THIS METHOD IS VERY SENSITIVE TO BLAST FORMATTING CHANGES!
:
: Removal of the HTML tags and accurate reconstitution of the
: non-HTML-formatted report is highly dependent on structure of
: the HTML-formatted version. For example, it assumes that first
: line of each alignment section (HSP listing) starts with a
: <a name=..> anchor tag. This permits the reconstruction of the
: original report in which these lines begin with a ">".
: This is required for parsing.
:
: If the structure of the Blast report itself is not intended to
: be a standard, the structure of the HTML-formatted version
: is even less so. Therefore, the use of this method to
: reconstitute parsable Blast reports from HTML-format versions
: should be considered a temorary solution.result2hash
Title : result2hash
Usage : my %data = &FAST::Bio::Search::SearchUtils($result)
Function : converts ResultI data to simple hash
Returns : hash
Args : ResultI
Note : used mainly as a utility for running SearchIO tests