bio-polyploid-tools 0.5.1 → 0.5.2

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data/VERSION CHANGED
@@ -1 +1 @@
1
- 0.5.1
1
+ 0.5.2
@@ -79,8 +79,9 @@ OptionParser.new do |opts|
79
79
 
80
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  opts.on("-p", "--primer_3_preferences FILE", "file with preferences to be sent to primer3") do |o|
81
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  options[:primer_3_preferences] = Bio::DB::Primer3.read_primer_preferences(o, options[:primer_3_preferences] )
82
-
83
82
  end
83
+
84
+
84
85
 
85
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  end.parse!
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87
 
@@ -2,16 +2,16 @@
2
2
  # DO NOT EDIT THIS FILE DIRECTLY
3
3
  # Instead, edit Jeweler::Tasks in Rakefile, and run 'rake gemspec'
4
4
  # -*- encoding: utf-8 -*-
5
- # stub: bio-polyploid-tools 0.5.1 ruby lib
5
+ # stub: bio-polyploid-tools 0.5.2 ruby lib
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6
 
7
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  Gem::Specification.new do |s|
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  s.name = "bio-polyploid-tools"
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- s.version = "0.5.1"
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+ s.version = "0.5.2"
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10
 
11
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  s.required_rubygems_version = Gem::Requirement.new(">= 0") if s.respond_to? :required_rubygems_version=
12
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  s.require_paths = ["lib"]
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  s.authors = ["Ricardo H. Ramirez-Gonzalez"]
14
- s.date = "2014-10-14"
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+ s.date = "2014-10-28"
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  s.description = "Repository of tools developed in TGAC and Crop Genetics in JIC to work with polyploid wheat"
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  s.email = "ricardo.ramirez-gonzalez@tgac.ac.uk"
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  s.executables = ["bfr.rb", "count_variations.rb", "filter_blat_by_target_coverage.rb", "find_best_blat_hit.rb", "find_best_exonerate.rb", "hexaploid_primers.rb", "homokaryot_primers.rb", "map_markers_to_contigs.rb", "markers_in_region.rb", "polymarker.rb", "snp_position_to_polymarker.rb", "snps_between_bams.rb"]
@@ -1,6 +1,6 @@
1
1
  module Bio::PolyploidTools
2
2
  class PrimerRegion
3
- attr_accessor :snp_pos, :sequence, :chromosome_specific, :almost_chromosome_specific, :crhomosome_specific_intron , :almost_crhomosome_specific_intron, :homeologous
3
+ attr_accessor :snp_pos, :sequence, :chromosome_specific, :almost_chromosome_specific, :crhomosome_specific_intron , :almost_crhomosome_specific_intron, :homoeologous
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4
 
5
5
  def initialize
6
6
 
@@ -203,11 +203,11 @@ module Bio::PolyploidTools
203
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  when mask[i] == '&'
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  #This is the SNP we take the parental
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  pr.snp_pos = position_in_region
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- pr.homeologous = false
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+ pr.homoeologous = false
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  when mask[i] == ':'
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  #This is the SNP we take the parental
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  pr.snp_pos = position_in_region
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- pr.homeologous = true
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+ pr.homoeologous = true
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  when mask[i] == '-'
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  #When the mask doesnt detect a SNP, so we take the parental
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  parental[i] = chromosome_seq[i] unless Bio::NucleicAcid::is_unambiguous(parental[i])
@@ -304,10 +304,10 @@ module Bio::PolyploidTools
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  rev_pos = seq_snp.size - position
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- if pr.homeologous
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- snp_type = "homeologous"
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+ if pr.homoeologous
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+ snp_type = "homoeologous"
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  else
310
- snp_type = "non-homeologous"
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+ snp_type = "non-homoeologous"
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  end
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  pr.chromosome_specific.each do |pos|
@@ -471,10 +471,10 @@ module Bio::DB::Primer3
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  @exon = false
472
472
  end
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473
 
474
- if @polymorphism.to_sym == :homeologous
475
- @homeologous = true
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+ if @polymorphism.to_sym == :homoeologous
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+ @homoeologous = true
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476
  else
477
- @homeologous = false
477
+ @homoeologous = false
478
478
  end
479
479
  @parsed = true
480
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  @orientation = @orientation.to_sym
@@ -492,10 +492,10 @@ module Bio::DB::Primer3
492
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  @chromosome
493
493
  end
494
494
 
495
- def homeologous?
496
- return @homeologous if @parsed
495
+ def homoeologous?
496
+ return @homoeologous if @parsed
497
497
  parse_header
498
- @homeologous
498
+ @homoeologous
499
499
  end
500
500
 
501
501
  def type
metadata CHANGED
@@ -1,14 +1,14 @@
1
1
  --- !ruby/object:Gem::Specification
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2
  name: bio-polyploid-tools
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3
  version: !ruby/object:Gem::Version
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- version: 0.5.1
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+ version: 0.5.2
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5
  platform: ruby
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  authors:
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7
  - Ricardo H. Ramirez-Gonzalez
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8
  autorequire:
9
9
  bindir: bin
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  cert_chain: []
11
- date: 2014-10-14 00:00:00.000000000 Z
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+ date: 2014-10-28 00:00:00.000000000 Z
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12
  dependencies:
13
13
  - !ruby/object:Gem::Dependency
14
14
  name: bio