fixed unit tests

[biopieces.git] / code_ruby / lib / maasha / seq.rb

# Copyright (C) 2007-2012 Martin A. Hansen.

# This program is free software; you can redistribute it and/or
# modify it under the terms of the GNU General Public License
# as published by the Free Software Foundation; either version 2
# of the License, or (at your option) any later version.

# This program is distributed in the hope that it will be useful,
# but WITHOUT ANY WARRANTY; without even the implied warranty of
# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE.  See the
# GNU General Public License for more details.

# You should have received a copy of the GNU General Public License
# along with this program; if not, write to the Free Software
# Foundation, Inc., 51 Franklin Street, Fifth Floor, Boston, MA 02110-1301, USA.

# http://www.gnu.org/copyleft/gpl.html

# >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>><<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<

# This software is part of the Biopieces framework (www.biopieces.org).

# >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>><<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<

require 'maasha/bits'
require 'maasha/seq/digest'
require 'maasha/seq/trim'
require 'narray'

autoload :BackTrack, 'maasha/seq/backtrack.rb'
autoload :Dynamic,   'maasha/seq/dynamic.rb'

# Residue alphabets
DNA     = %w[a t c g]
RNA     = %w[a u c g]
PROTEIN = %w[f l s y c w p h q r i m t n k v a d e g]
INDELS  = %w[. - _ ~]

# Translation table 11
# (http://www.ncbi.nlm.nih.gov/Taxonomy/taxonomyhome.html/index.cgi?chapter=cgencodes#SG11)
#   AAs  = FFLLSSSSYY**CC*WLLLLPPPPHHQQRRRRIIIMTTTTNNKKSSRRVVVVAAAADDEEGGGG
# Starts = ---M---------------M------------MMMM---------------M------------
# Base1  = TTTTTTTTTTTTTTTTCCCCCCCCCCCCCCCCAAAAAAAAAAAAAAAAGGGGGGGGGGGGGGGG
# Base2  = TTTTCCCCAAAAGGGGTTTTCCCCAAAAGGGGTTTTCCCCAAAAGGGGTTTTCCCCAAAAGGGG
# Base3  = TCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAG
TRANS_TAB11_START = {
  "TTG" => "M", "CTG" => "M", "ATT" => "M", "ATC" => "M",
  "ATA" => "M", "ATG" => "M", "GTG" => "M"
}

TRANS_TAB11 = {
  "TTT" => "F", "TCT" => "S", "TAT" => "Y", "TGT" => "C",
  "TTC" => "F", "TCC" => "S", "TAC" => "Y", "TGC" => "C",
  "TTA" => "L", "TCA" => "S", "TAA" => "*", "TGA" => "*",
  "TTG" => "L", "TCG" => "S", "TAG" => "*", "TGG" => "W",
  "CTT" => "L", "CCT" => "P", "CAT" => "H", "CGT" => "R",
  "CTC" => "L", "CCC" => "P", "CAC" => "H", "CGC" => "R",
  "CTA" => "L", "CCA" => "P", "CAA" => "Q", "CGA" => "R",
  "CTG" => "L", "CCG" => "P", "CAG" => "Q", "CGG" => "R",
  "ATT" => "I", "ACT" => "T", "AAT" => "N", "AGT" => "S",
  "ATC" => "I", "ACC" => "T", "AAC" => "N", "AGC" => "S",
  "ATA" => "I", "ACA" => "T", "AAA" => "K", "AGA" => "R",
  "ATG" => "M", "ACG" => "T", "AAG" => "K", "AGG" => "R",
  "GTT" => "V", "GCT" => "A", "GAT" => "D", "GGT" => "G",
  "GTC" => "V", "GCC" => "A", "GAC" => "D", "GGC" => "G",
  "GTA" => "V", "GCA" => "A", "GAA" => "E", "GGA" => "G",
  "GTG" => "V", "GCG" => "A", "GAG" => "E", "GGG" => "G"
}

# Quality scores bases
SCORE_BASE = 64
SCORE_MIN  = 0
SCORE_MAX  = 40

# Error class for all exceptions to do with Seq.
class SeqError < StandardError; end

class Seq
  include Digest
  include Trim

  attr_accessor :seq_name, :seq, :type, :qual

  # Class method to instantiate a new Sequence object given
  # a Biopiece record.
  def self.new_bp(record)
    seq_name = record[:SEQ_NAME]
    seq      = record[:SEQ]
    type     = record[:SEQ_TYPE]
    qual     = record[:SCORES]

    self.new(seq_name, seq, type, qual)
  end

  # Class method that generates all possible oligos of a specifed length and type.
  def self.generate_oligos(length, type)
    raise SeqError, "Cannot generate negative oligo length: #{length}" if length <= 0

    case type.downcase
    when /dna/     then alph = DNA
    when /rna/     then alph = RNA
    when /protein/ then alph = PROTEIN
    else
      raise SeqError, "Unknown sequence type: #{type}"
    end

    oligos = [""]

    (1 .. length).each do
      list = []

      oligos.each do |oligo|
        alph.each do |char|
          list << oligo + char
        end
      end

      oligos = list
    end

    oligos
  end

  # Initialize a sequence object with the following arguments:
  # - seq_name: Name of the sequence.
  # - seq: The sequence.
  # - type: The sequence type - DNA, RNA, or protein
  # - qual: An Illumina type quality scores string.
  def initialize(seq_name = nil, seq = nil, type = nil, qual = nil)
    @seq_name = seq_name
    @seq      = seq
    @type     = type
    @qual     = qual
  end

  # Method that guesses and returns the sequence type
  # by inspecting the first 100 residues.
  def type_guess
    raise SeqError, "Guess failed: sequence is nil" if self.seq.nil?

    case self.seq[0 ... 100].downcase
    when /[flpqie]/ then return "protein"
    when /[u]/      then return "rna"
    else                 return "dna"
    end
  end

  # Method that guesses and sets the sequence type
  # by inspecting the first 100 residues.
  def type_guess!
    self.type = self.type_guess
  end

  # Returns the length of a sequence.
  def length
    self.seq.nil? ? 0 : self.seq.length
  end

  alias :len :length

  # Return the number indels in a sequence.
  def indels
    regex = Regexp.new(/[#{Regexp.escape(INDELS.join(""))}]/)
    self.seq.scan(regex).size
  end

  # Method to remove indels from seq and qual if qual.
  def indels_remove
    if self.qual.nil?
      self.seq.delete!(Regexp.escape(INDELS.join('')))
    else
      na_seq  = NArray.to_na(self.seq, "byte")
      na_qual = NArray.to_na(self.qual, "byte")
      mask    = NArray.byte(self.length)

      INDELS.each do |c|
        mask += na_seq.eq(c.ord)
      end

      mask = mask.eq(0)

      self.seq  = na_seq[mask].to_s
      self.qual = na_qual[mask].to_s
    end

    self
  end

  # Method that returns true is a given sequence type is DNA.
  def is_dna?
    self.type == 'dna'
  end

  # Method that returns true is a given sequence type is RNA.
  def is_rna?
    self.type == 'rna'
  end

  # Method that returns true is a given sequence type is protein.
  def is_protein?
    self.type == 'protein'
  end

  # Method to transcribe DNA to RNA.
  def to_rna
    raise SeqError, "Cannot transcribe 0 length sequence" if self.length == 0
    raise SeqError, "Cannot transcribe sequence type: #{self.type}" unless self.is_dna?
    self.type = 'rna'
    self.seq.tr!('Tt','Uu')
  end

  # Method to reverse-transcribe RNA to DNA.
  def to_dna
    raise SeqError, "Cannot reverse-transcribe 0 length sequence" if self.length == 0
    raise SeqError, "Cannot reverse-transcribe sequence type: #{self.type}" unless self.is_rna?

    self.type = 'dna'
    self.seq.tr!('Uu','Tt')
  end

  # Method to translate a DNA sequence to protein.
  def translate!(trans_tab = 11)
    raise SeqError, "Sequence type must be 'dna' - not #{self.type}" unless self.type == 'dna'
    raise SeqError, "Sequence length must be a multiplum of 3 - was: #{self.length}" unless (self.length % 3) == 0

    case trans_tab
    when 11
      codon_start_hash = TRANS_TAB11_START
      codon_hash       = TRANS_TAB11
    else
      raise SeqError, "Unknown translation table: #{trans_tab}"
    end

    codon  = self.seq[0 ... 3].upcase

    aa = codon_start_hash[codon]

    raise SeqError, "Unknown start codon: #{codon}" if aa.nil?

    protein = aa

    i = 3

    while i < self.length
      codon = self.seq[i ... i + 3].upcase

      aa = codon_hash[codon]

      raise SeqError, "Unknown codon: #{codon}" if aa.nil?

      protein << aa

      i += 3
    end

    self.seq  = protein
    self.qual = nil
    self.type = "protein"

    self
  end

  alias :to_protein! :translate!

  def translate(trans_tab = 11)
    self.dup.translate!(trans_tab)
  end

  alias :to_protein :translate

  # Method that given a Seq entry returns a Biopieces record (a hash).
  def to_bp
    raise SeqError, "Missing seq_name" if self.seq_name.nil?
    raise SeqError, "Missing seq"      if self.seq.nil?

    record             = {}
    record[:SEQ_NAME] = self.seq_name
    record[:SEQ]      = self.seq
    record[:SEQ_LEN]  = self.length
    record[:SCORES]   = self.qual if self.qual
    record
  end

  # Method that given a Seq entry returns a FASTA entry (a string).
  def to_fasta(wrap = nil)
    raise SeqError, "Missing seq_name" if self.seq_name.nil? or self.seq_name == ''
    raise SeqError, "Missing seq"      if self.seq.nil?      or self.seq.empty?

    seq_name = self.seq_name.to_s
    seq      = self.seq.to_s

    unless wrap.nil?
      seq.gsub!(/(.{#{wrap}})/) do |match|
        match << $/
      end

      seq.chomp!
    end

    ">" + seq_name + $/ + seq + $/
  end

  # Method that given a Seq entry returns a FASTQ entry (a string).
  def to_fastq
    raise SeqError, "Missing seq_name" if self.seq_name.nil?
    raise SeqError, "Missing seq"      if self.seq.nil?
    raise SeqError, "Missing qual"     if self.qual.nil?

    seq_name = self.seq_name.to_s
    seq      = self.seq.to_s
    qual     = self.qual.to_s

    "@" + seq_name + $/ + seq + $/ + "+" + $/ + qual + $/
  end

  # Method that generates a unique key for a
  # DNA sequence and return this key as a Fixnum.
  def to_key
    key = 0
    
    self.seq.upcase.each_char do |char|
      key <<= 2
      
      case char
      when 'A' then key |= 0
      when 'C' then key |= 1
      when 'G' then key |= 2
      when 'T' then key |= 3
      else raise SeqError, "Bad residue: #{char}"
      end
    end
    
    key
  end

  # Method to reverse complement sequence.
  def reverse_complement
    self.reverse
    self.complement
    self
  end

  alias :revcomp :reverse_complement

  # Method to reverse the sequence.
  def reverse
    self.seq.reverse!
    self.qual.reverse! if self.qual
    self
  end

  # Method that complements sequence including ambiguity codes.
  def complement
    raise SeqError, "Cannot complement 0 length sequence" if self.length == 0

    if self.is_dna?
      self.seq.tr!('AGCUTRYWSMKHDVBNagcutrywsmkhdvbn', 'TCGAAYRWSKMDHBVNtcgaayrwskmdhbvn')
    elsif self.is_rna?
      self.seq.tr!('AGCUTRYWSMKHDVBNagcutrywsmkhdvbn', 'UCGAAYRWSKMDHBVNucgaayrwskmdhbvn')
    else
      raise SeqError, "Cannot complement sequence type: #{self.type}"
    end
  end

  # Method to determine the Hamming Distance between
  # two Sequence objects (case insensitive).
  def hamming_distance(seq)
    self.seq.upcase.hamming_distance(seq.seq.upcase)
  end

  # Method that generates a random sequence of a given length and type.
  def generate(length, type)
    raise SeqError, "Cannot generate sequence length < 1: #{length}" if length <= 0

    case type.downcase
    when "dna"
      alph = DNA
    when "rna"
      alph = RNA
    when "protein"
      alph = PROTEIN
    else
      raise SeqError, "Unknown sequence type: #{type}"
    end

    seq_new   = Array.new(length) { alph[rand(alph.size)] }.join("")
    self.seq  = seq_new
    self.type = type.downcase
    seq_new
  end

  # Method to shuffle a sequence readomly inline.
  def shuffle!
    self.seq = self.seq.split('').shuffle!.join
    self
  end

  # Method that returns a subsequence of from a given start position
  # and of a given length.
  def subseq(start, length = self.length - start)
    raise SeqError, "subsequence start: #{start} < 0"                                                if start  < 0
    raise SeqError, "subsequence length: #{length} < 0"                                              if length < 0
    raise SeqError, "subsequence start + length > Seq.length: #{start} + #{length} > #{self.length}" if start + length > self.length

    if length == 0
      seq  = ""
      qual = "" unless self.qual.nil?
    else
      stop = start + length - 1

      seq  = self.seq[start .. stop]
      qual = self.qual[start .. stop] unless self.qual.nil?
    end

    Seq.new(self.seq_name, seq, self.type, qual)    # TODO changed self.seq_name.dup to self.seq_name -> consequence?
  end

  # Method that replaces a sequence with a subsequence from a given start position
  # and of a given length.
  def subseq!(start, length = self.length - start)
    s = subseq(start, length)

    self.seq_name = s.seq_name
    self.seq      = s.seq
    self.type     = s.type
    self.qual     = s.qual

    self
  end

  # Method that returns a subsequence of a given length
  # beginning at a random position.
  def subseq_rand(length)
    if self.length - length + 1 == 0
      start = 0
    else
      start = rand(self.length - length + 1)
    end

    self.subseq(start, length)
  end

  # Method that returns the residue compositions of a sequence in
  # a hash where the key is the residue and the value is the residue
  # count.
  def composition
    comp = Hash.new(0);

    self.seq.upcase.each_char do |char|
      comp[char] += 1
    end

    comp
  end

  # Method that returns the length of the longest homopolymeric stretch
  # found in a sequence.
  def homopol_max(min = 1)
    return 0 if self.seq.nil? or self.seq.empty?

    found = false

    self.seq.upcase.scan(/A{#{min},}|T{#{min},}|G{#{min},}|C{#{min},}|N{#{min},}/) do |match|
      found = true
      min   = match.size > min ? match.size : min
    end

    return 0 unless found
 
    min
  end

  # Method that returns the percentage of hard masked residues
  # or N's in a sequence.
  def hard_mask
    ((self.seq.upcase.scan("N").size.to_f / (self.len - self.indels).to_f) * 100).round(2)
  end

  # Method that returns the percentage of soft masked residues
  # or lower cased residues in a sequence.
  def soft_mask
    ((self.seq.scan(/[a-z]/).size.to_f / (self.len - self.indels).to_f) * 100).round(2)
  end

  # Hard masks sequence residues where the corresponding quality score
  # is below a given cutoff.
  def mask_seq_hard_old(cutoff)
    seq    = self.seq.upcase
    scores = self.qual
    i      = 0

    scores.each_char do |score|
      seq[i] = 'N' if score.ord - SCORE_BASE < cutoff
      i += 1 
    end

    self.seq = seq
  end

  # Hard masks sequence residues where the corresponding quality score
  # is below a given cutoff.
  def mask_seq_hard!(cutoff)
    raise SeqError, "seq is nil"  if self.seq.nil?
    raise SeqError, "qual is nil" if self.qual.nil?
    raise SeqError, "cufoff value: #{cutoff} out of range #{SCORE_MIN} .. #{SCORE_MAX}" unless (SCORE_MIN .. SCORE_MAX).include? cutoff

    na_seq  = NArray.to_na(self.seq, "byte")
    na_qual = NArray.to_na(self.qual, "byte")
    mask    = (na_qual - SCORE_BASE) < cutoff
    mask   *= na_seq.ne("-".ord)

    na_seq[mask] = 'N'.ord

    self.seq = na_seq.to_s

    self
  end

  # Soft masks sequence residues where the corresponding quality score
  # is below a given cutoff.
  def mask_seq_soft!(cutoff)
    raise SeqError, "seq is nil"  if self.seq.nil?
    raise SeqError, "qual is nil" if self.qual.nil?
    raise SeqError, "cufoff value: #{cutoff} out of range #{SCORE_MIN} .. #{SCORE_MAX}" unless (SCORE_MIN .. SCORE_MAX).include? cutoff

    na_seq  = NArray.to_na(self.seq, "byte")
    na_qual = NArray.to_na(self.qual, "byte")
    mask    = (na_qual - SCORE_BASE) < cutoff
    mask   *= na_seq.ne("-".ord)

    na_seq[mask] ^= ' '.ord

    self.seq = na_seq.to_s

    self
  end

  # Method that determines if a quality score string can be
  # absolutely identified as base 33.
  def qual_base33?
    self.qual.match(/[!-:]/)
  end

  # Method that determines if a quality score string can be
  # absolutely identified as base 64.
  def qual_base64?
    self.qual.match(/[K-h]/)
  end

  # Method to convert quality scores inbetween formats.
  # Sanger     base 33, range  0-40 
  # 454        base 64, range  0-40 
  # Solexa     base 64, range -5-40 
  # Illumina13 base 64, range  0-40 
  # Illumina15 base 64, range  3-40 
  # Illumina18 base 33, range  0-41 
  def convert_scores!(from, to)
    unless from == to
      na_qual = NArray.to_na(self.qual, "byte")

      case from.downcase
      when "sanger"     then na_qual -= 33
      when "454"        then na_qual -= 64
      when "solexa"     then na_qual -= 64
      when "illumina13" then na_qual -= 64
      when "illumina15" then na_qual -= 64
      when "illumina18" then na_qual -= 33
      else raise SeqError, "unknown quality score encoding: #{from}"
      end

      case to.downcase
      when "sanger"     then na_qual += 33
      when "454"        then na_qual += 64
      when "solexa"     then na_qual += 64
      when "illumina13" then na_qual += 64
      when "illumina15" then na_qual += 64
      when "illumina18" then na_qual += 33
      else raise SeqError, "unknown quality score encoding: #{from}"
      end

      self.qual = na_qual.to_s
    end

    self
  end

  # Method to calculate and return the mean quality score.
  def scores_mean
    raise SeqError, "Missing qual in entry" if self.qual.nil?

    na_qual = NArray.to_na(self.qual, "byte")
    na_qual -= SCORE_BASE
    na_qual.mean
  end

  # Method to find open reading frames (ORFs).
  def each_orf(size_min, size_max, start_codons, stop_codons, pick_longest = false)
    orfs    = []
    pos_beg = 0

    regex_start = Regexp.new(start_codons.join('|'), true)
    regex_stop  = Regexp.new(stop_codons.join('|'), true)

    while pos_beg and pos_beg < self.length - size_min
      if pos_beg = self.seq.index(regex_start, pos_beg)
        if pos_end = self.seq.index(regex_stop, pos_beg)
          length = (pos_end - pos_beg) + 3

          if (length % 3) == 0
            if size_min <= length and length <= size_max
              subseq = self.subseq(pos_beg, length)

              orfs << [subseq, pos_beg, pos_end + 3]
            end
          end
        end

        pos_beg += 1
      end
    end

    if pick_longest
      orf_hash = {}

      orfs.each { |orf| orf_hash[orf.last] = orf unless orf_hash[orf.last] }

      orfs = orf_hash.values
    end

    if block_given?
      orfs.each { |orf| yield orf }
    else
      return orfs
    end
  end
end

__END__