NAME

Bio::Polloc::GroupCriteria - Rules to group loci

DESCRIPTION

Takes loci and returns groups of loci based on certain rules. If created via .bme (.cfg) files, it is defined in the [ RuleGroup ] and [ GroupExtension ] namespaces.

AUTHOR - Luis M. Rodriguez-R

Email lmrodriguezr at gmail dot com

LICENSE

This package is licensed under the Artistic License - see LICENSE.txt

IMPLEMENTS OR EXTENDS

APPENDIX - Methods

Methods provided by the package

new

  • Generic initialization method

  • Arguments

    -souce str

    See source

    -target str

    See target

    -features Bio::Polloc::LociGroup

    Alias of -loci

    -loci Bio::Polloc::LociGroup

    See locigroup

  • Returns

    The Bio::Polloc::GroupCriteria object

source

target

locigroup

condition

  • Sets/gets the conditions set to evaluate.

evaluate

get_loci

  • Gets the stored loci

  • Note

    The stored loci can also be obtained with $object->locigroup->loci, but this function ensures a consistent order in the loci for its evaluation.

get_locus

  • Get the locus with the specified index.

  • Arguments

    The index (int, mandatory).

  • Returns

    A Bio::Polloc::LocusI object or undef.

  • Note

    This is a lazzy method, and should be used ONLY after get_loci() were called at least once. Otherwise, the order might not be the expected, and weird results would appear.

extension

  • Sets the conditions for group extensions.

  • Arguments

    Array, hash or string with -key => value pairs. Supported values are:

    -function str
    context

    Searches the flanking regions in the target sequence.

    -upstream int

    Extension in number of residues upstream the feature.

    -downstream int

    Extension in number of residues downstream the feature.

    -detectstrand bool (int)

    Should I detect the proper strand? Otherwise, the stored strand is trusted. This is useful for non-directed features like repeats, which context is actually directed.

    -alldetected bool (int)

    Include all detected features (even these overlapping with input features).

    -feature bool (int)

    Should I include the feature region in the search? 0 by default.

    -lensd float

    Number of Standar Deviations (SD) tolerated as half of the range of lengths for a feature. The average (Avg) and the standard deviation of the length are calculated based on all the stored features, and the Avg+(SD*lensd) is considered as the largest possible new feature. No minimum length constraint is given, unless explicitly set with -minlen. This argument is ignored if -maxlen is explicitly set. Default is 1.5.

    -maxlen int

    Maximum length of a new feature in number of residues. If zero (0) evaluates -lensd instead. Default is 0.

    -minlen int

    Minimum length of a new feature in number of residues. Default is 0.

    -similarity float

    Minimum fraction of similarity to include a found region. 0.8 by default.

    -oneside bool (int)

    Should I consider features with only one of the sides? Takes effect only if both -upstream and -downstream are defined. 0 by default.

    -algorithm str
    blast

    Use BLAST to search (after multiple alignment and consensus calculation of queries). Default algorithm.

    hmmer

    Use HMMer to search (after multiple alignment and hmmbuild of query sequences).

    -score int

    Minimum score for either algorithms blast and hmmer. 20 by default.

    -consensusperc float

    Minimum percentage a residue must appear in order to include it in the consensus used as query. 60 by default. Only if -algorithm blast.

    -e float

    If -algorithm blast, maximum e-value. 0.1 by default.

    -p str

    If -algorithm blast, program used ([t]blast[npx]). blastn by default.

  • Throws

    Bio::Polloc::Polloc::Error if unexpected input,

extend

build_bin

  • Compares all the included loci and returns the identity matrix

  • Arguments

    -complete bool (int)

    If true, calculates the complete matrix instead of only the bottom-left triangle.

  • Returns

    A reference to a boolean 2-dimensional array (only left-down triangle)

  • Note

    WARNING! The order of the output is not allways the same of the input. Please use get_loci() instead, as source features MUST be after target features in the array. Otherwise, it is not possible to have the full picture without building the full matrix (instead of half).

bin_build_groups

  • Builds groups of loci based on a binary matrix

  • Arguments

    A matrix as returned by Bio::Polloc::GroupCriteria->build_bin

  • Returns

    A 2-D arrayref.

  • Note

    This method is intended to build groups providing information on all-vs-all comparisons. If you do not need this information, use the much more efficient Bio::Polloc::GroupCriteria->build_groups method, that relies on transitive property of groups to avoid unnecessary comparisons. Please note that this function also relies on transitivity, but gives you the option to examine all the paired comparisons and even write your own grouping function.

build_groups

  • This is the main method, creates groups of loci.

  • Arguments

    -cpus int

    If defined, attempts to distribute the work among the specified number of cores. Warning: This parameter is experimental, and relies on Parallel::ForkManager. It can be used in production with certain confidence, but it is highly probable to NOT work in parallel (to avoid errors, this method ignores the command at ANY possible error).

    Unimplemented: This argument is currently ignored. Some algorithmic considerations must be addressed before using it. TODO.

    -advance coderef

    A reference to a function to call at every new pair. The function is called with three arguments, the first is the index of the first locus, the second is the index of the second locus and the third is the total number of loci. Note that this function is called BEFORE running the comparison.

  • Returns

    An arrayref of Bio::Polloc::LociGroup objects, each containing one consistent group of loci.

  • Note

    This method is faster than combining build_bin() and build_groups_bin(), and it should be used whenever transitivity can be freely assumed and you do not need the all-vs-all matrix for further evaluation (for example, manual inspection).

genomes

  • Gets the genomes of the base group of loci. This function is similar to calling locigroup()->genomes(), but is read-only.

INTERNAL METHODS

Methods intended to be used only within the scope of Bio::Polloc::*

_detect_border_pairs

_next_group_id

  • Returns an incremental ID that attempts to identify the group used as basis of extension. Please note that this method DOES NOT check if the group's ID is the right one, and it is basically intended to keep track of how many times the extend function has been called.

_build_subseq

Arguments

All the following arguments are mandatory and must be passed in that order. The strand will be determined by the relative position of from/to:

  • The sequence (Bio::Seq object).

  • The from position (int).

  • The to position (int).

Returns

A Bio::Seq object.

Comments

This method should be located at a higher hierarchy module (Root?).

This method is static.

_search_aln_seqs

  • Uses an alignment to search in the sequences of the collection of genomes

  • Arguments

    A Bio::SimpleAlign object

  • Returns

    A 2D arrayref, where first key is an incremental and second key preserves the orrder in the structure: ["genome-key:acc", from, to, strand, score]

_feat_index2obj

_grouprules_cleanup

_initialize

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