bio-polyploid-tools 0.7.2 → 0.7.3

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data/README.md CHANGED
@@ -69,12 +69,16 @@ arm_selection_functions[:arm_selection_embl] = lambda do | contig_name|
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  end
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  ```
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- The function should return a 2 character string, when the first is the chromosome number and the second the chromosome group. The symbol in the hash is the name to be used in the argument ```--arm_selection```. If you want your parser to be added to the distribution, feel free to fork and make a pull request.
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+ The function should return a 2 character string, when the first is the chromosome number and the second the chromosome group. The symbol in the hash is the name to be used in the argument ```--arm_selection```. If you want your parser to be added to the distribution, feel free to fork and make a pull request.
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  ##Release Notes
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+ ###0.7.3
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+ * FEATURE: ```polymarker.rb``` Added to the flag ```--arm_selection``` the option ```scaffold```, which now supports a scaffold specific primer.
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+ * FEATURE: ```snp_position_to_polymarker``` Added the option ```--mutant_list``` to prepare files for PolyMarker from files with the following columns ```ID,Allele_1,position,Allele_1,target_chromosome```.
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+
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  ###0.7.2
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  * FEATURE: Added a flag ```min_identity``` to set the minimum identity to consider a hit. The default is 90
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data/VERSION CHANGED
@@ -1 +1 @@
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- 0.7.2
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+ 0.7.3
@@ -24,7 +24,7 @@ markers = nil
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  options = {}
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  OptionParser.new do |opts|
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- opts.banner = "Usage: polymarker.rb [options]"
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+ opts.banner = "Usage: markers_in_region.rb [options]"
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  opts.on("-c", "--chromosome CHR", "chromosome (1A, 3B, etc)") do |o|
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  options[:chromosome] = o.upcase
@@ -37,6 +37,11 @@ arm_selection_functions[:arm_selection_morex] = lambda do | contig_name |
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  return ret
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  end
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+ arm_selection_functions[:scaffold] = lambda do | contig_name |
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+ ret = contig_name;
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+ return ret
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+ end
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+
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  def validate_files(o)
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  [
@@ -113,7 +118,7 @@ OptionParser.new do |opts|
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  options[:model] = o
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  end
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- opts.on("-a", "--arm_selection arm_selection_embl|arm_selection_morex|arm_selection_first_two", "Function to decide the chromome arm") do |o|
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+ opts.on("-a", "--arm_selection arm_selection_embl|arm_selection_morex|arm_selection_first_two|scaffold", "Function to decide the chromome arm") do |o|
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  options[:arm_selection] = arm_selection_functions[o.to_sym];
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  end
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@@ -24,12 +24,14 @@ markers = nil
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  options = {}
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  options[:flanking_size] = 100
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+ test_file=''
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  OptionParser.new do |opts|
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  opts.banner = "Usage: snp_postion_to_polymarker.rb [options]"
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  opts.on("-s", "--snp_file CSV", "CSV file with the following columnns:\nID,Allele_1,position,Allele_1,target_chromosome") do |o|
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  options[:snp_file] = o
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+ test_file = o
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  end
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  opts.on("-r", "--reference FASTA", "reference with the genes/contings/marker seuqnece") do |o|
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  options[:reference] = o
@@ -40,6 +42,11 @@ OptionParser.new do |opts|
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  opts.on("-f", "--flanking_size INT", "Flanking size around the SNP") do |o|
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  options[:flanking_size] = o.to_i
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  end
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+ opts.on("-t", "--mutant_list FILE", "File with the list of positions with mutation and the mutation line.\n\
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+ requires --reference to get the sequence using a position") do |o|
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+ options[:mutant_list] = o
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+ test_file = o
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+ end
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  end.parse!
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  #reference="/Users/ramirezr/Documents/TGAC/references/Triticum_aestivum.IWGSP1.21.dna_rm.genome.fa"
@@ -49,16 +56,28 @@ fasta_reference_db = Bio::DB::Fasta::FastaFile.new({:fasta=>fasta_reference})
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  fasta_reference_db.load_fai_entries
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  out = $stdout
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+ lastRegion = nil
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+ lastTemplate = nil
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  out = File.open(options[:output], "w") if options[:output]
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- File.open(options[:snp_file]) do | f |
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+ File.open(test_file) do | f |
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  f.each_line do | line |
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  snp = nil
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- snp = Bio::PolyploidTools::SNP.parse(line)
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- entry = fasta_reference_db.index.region_for_entry(snp.gene)
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+ entry = nil
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+ if options[:snp_file]
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+ snp = Bio::PolyploidTools::SNP.parse(line)
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+ entry = fasta_reference_db.index.region_for_entry(snp.gene)
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+ elsif options[:mutant_list]
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+ snp = Bio::PolyploidTools::SNPMutant.parse(line)
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+ entry = fasta_reference_db.index.region_for_entry(snp.contig)
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+ end
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+
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  if entry
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- region = fasta_reference_db.index.region_for_entry(snp.gene).get_full_region
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- snp.template_sequence = fasta_reference_db.fetch_sequence(region)
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-
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+ region = entry.get_full_region
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+ if region != lastRegion
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+ lastTemplate = fasta_reference_db.fetch_sequence(region)
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+ end
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+ snp.template_sequence = lastTemplate
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+ lastRegion = region
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  out.puts "#{snp.gene}_#{snp.snp_id_in_seq},#{snp.chromosome},#{snp.to_polymarker_sequence(options[:flanking_size])}"
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  else
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  $stderr.puts "ERROR: Unable to find entry for #{snp.gene}"
@@ -2,16 +2,16 @@
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  # DO NOT EDIT THIS FILE DIRECTLY
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  # Instead, edit Jeweler::Tasks in Rakefile, and run 'rake gemspec'
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  # -*- encoding: utf-8 -*-
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- # stub: bio-polyploid-tools 0.7.2 ruby lib
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+ # stub: bio-polyploid-tools 0.7.3 ruby lib
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  Gem::Specification.new do |s|
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  s.name = "bio-polyploid-tools"
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- s.version = "0.7.2"
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+ s.version = "0.7.3"
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  s.required_rubygems_version = Gem::Requirement.new(">= 0") if s.respond_to? :required_rubygems_version=
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  s.require_paths = ["lib"]
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  s.authors = ["Ricardo H. Ramirez-Gonzalez"]
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- s.date = "2015-05-28"
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+ s.date = "2015-08-10"
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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", "filter_exonerate_by_identity.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"]
metadata CHANGED
@@ -1,14 +1,14 @@
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  --- !ruby/object:Gem::Specification
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  name: bio-polyploid-tools
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  version: !ruby/object:Gem::Version
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- version: 0.7.2
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+ version: 0.7.3
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  platform: ruby
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  authors:
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  - Ricardo H. Ramirez-Gonzalez
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  autorequire:
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  bindir: bin
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  cert_chain: []
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- date: 2015-05-28 00:00:00.000000000 Z
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+ date: 2015-08-10 00:00:00.000000000 Z
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  dependencies:
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  - !ruby/object:Gem::Dependency
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  name: bio