Bio::S...hUtils(3pm)

πŸ“¦
version 1.7.8 Β· 3 versions
, in debian bookworm, debian trixie, ubuntu jammy, ubuntu noble

✨ NAME ✨

Bio::Search::SearchUtils β€” utility functions for Bio::Search:: objects πŸ’–

This is the page for Bio::S...hUtils(3pm) β€” the SearchUtils manpage from the User Contributed Perl Documentation. Say hi to your new fave little toolbox, bestie 🧰✨


🌸 SYNOPSIS 🌸

okay so first thing you need to know:

# This module is just a collection of subroutines, not an object.

That's it. That's the whole synopsis. It's not an object, it's a pile of helpful little subs, and honestly? iconic behaviour πŸŽ€


πŸ¦‹ DESCRIPTION πŸ¦‹

The SearchUtils.pm module is a collection of subroutines used primarily by Bio::Search::Hit::HitI objects for some of the additional functionality, such as HSP tiling. Right now, SearchUtils is just a collection of methods, not an object. No blessed refs, no new(), no drama πŸ’…


πŸ‘‘ AUTHOR πŸ‘‘

Steve Chervitz <sac@bioperl.org> 🌟

πŸŽ€ CONTRIBUTORS πŸŽ€

Sendu Bala, <bix@sendu.me.uk> 🫢


🌈 tile_hsps 🌈

  • Usage β€” tile_hsps( $sbjct );

This one gets called automatically by methods in Bio::Search::Hit::GenericHit that rely on having tiled data, so you don't have to summon it yourself (usually).

But if you're nosy and want the data about the constructed HSP contigs, here's the whole vibe:

my ($qcontigs, $scontigs) = Bio::Search::SearchUtils::tile_hsps($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 info about the contig data structure πŸ‘‡

  • Purpose β€” collect statistics about the aligned sequences in a set of HSPs. It calculates the following data across all HSPs:
    • total alignment length
    • total identical residues
    • total conserved residues
  • Returns β€” depends on the situation, bestie:
    • 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 HSPs, tile_hsps() returns a list of two array references containing 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 these 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
not me noticing that 'stop' is documented as "start coordinate of the contig" β€” that is literally what the source says, I'm just the messenger πŸ™ˆ
  • Argument β€” a Bio::Search::Hit::HitI object
  • Throws β€” n/a (chill, no throwing here)
  • Comments β€”

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 (which is, like, 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. Slay πŸ’…

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. Lowkey plan for that ⏳

  • Bugs β€”
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 of 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 Bio::Search::Hit::GenericHit.

πŸ’€ so yeah, keep that overlap number smol, fr fr.

  • See Also β€” _adjust_contigs(), Bio::Search::Hit::GenericHit

πŸ¦‹ logical_length πŸ¦‹

  • Usage β€” logical_length( $alg_name, $seq_type, $length );
  • Purpose β€” determine the logical length of an aligned sequence based on algorithm name and sequence type.
  • Returns β€” integer representing the logical aligned length.
  • Argument β€”
    • $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 β€” n/a
  • Comments β€” 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 β€” &get_exponent( number );
  • Purpose β€” determines the power of 10 exponent of an integer, float, or scientific notation number.
  • Example β€”
&get_exponent("4.0e-206");
&get_exponent("0.00032");
&get_exponent("10.");
&get_exponent("1000.0");
&get_exponent("e+83");
  • Argument β€” Float, Integer, or scientific notation number
  • Returns β€” Integer representing the exponent part of the number (+ or -). If argument == 0 (zero), return value is "-999".
  • Comments β€” exponents are rounded up (less negative) if the mantissa is >= 5. Exponents are rounded down (more negative) if the mantissa is <= -5.

πŸŽ€ collapse_nums πŸŽ€

  • Usage β€” @cnums = collapse_nums( @numbers );
  • Purpose β€” collapses a list of numbers into a set of ranges of consecutive terms. Super 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 β€” list of numbers sorted numerically.
  • Returns β€” list of numbers mixed with ranges of numbers (see above).
  • Throws β€” n/a
  • See Also β€” Bio::Search::Hit::BlastHit::seq_inds()

πŸ’… strip_blast_html πŸ’…

  • Usage β€” $boolean = &strip_blast_html( string_ref );

This method is exported. πŸ“€

  • Purpose β€” removes HTML formatting from a supplied string. Attempts to restore the Blast report to enable parsing by Bio::SearchIO::blast.pm
  • Returns β€” Boolean: true if string was stripped, false if not.
  • Argument β€” string_ref = reference to a string containing the whole Blast report containing HTML formatting.
  • Throws β€” croaks if the argument is not a scalar reference.
  • Comments β€”
    • 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 temporary solution.


🌟 result2hash 🌟

  • Title β€” result2hash
  • Usage β€” my %data = &Bio::Search::SearchUtils($result)
  • Function β€” converts ResultI data to simple hash
  • Returns β€” hash
  • Args β€” ResultI
  • Note β€” used mainly as a utility for running SearchIO tests

and that's the whole page, bestie!! 🫢 this one came from perl v5.32.1, dated 2021-08-15, and it lives under the name Bio::S...hUtils(3pm). go tile some HSPs, you've got this πŸ’–βœ¨πŸŽ€

πŸ“¦ where this page comes from