#puts "Loading ExonCointainer..." module Bio::PolyploidTools class ExonContainer attr_reader :parental_1_sam, :parental_2_sam attr_reader :parental_1_name, :parental_2_name, :gene_models_db attr_reader :chromosomes, :snp_map attr_reader :parents attr_accessor :flanking_size , :primer_3_min_seq_length BASES = [:A, :C, :G, :T] #Sets the reference file for the gene models def initialize @parents=Hash.new @snp_map = Hash.new @snp_contigs @primer_3_min_seq_length = 50 end def gene_models(path) @gene_models_db = Bio::DB::Fasta::FastaFile.new({:fasta=>path}) @gene_models_db.index @gene_models_path = path end #Returns the sequence for a region in the gene models (exon) def gene_model_sequence(region) #puts "Region: " #puts region.inspect target_reg = @gene_models_db.index.region_for_entry(region.entry) #puts target_reg.inspect region.end = target_reg.length if region.end > target_reg.length #entries[region.entry] seq=@gene_models_db.fetch_sequence(region) #puts "sequence: " #This is a patch that we need to fix in biosamtools: #puts seq index = seq.index('>') if(index ) index -= 1 #puts "Index: #{index}" seq = seq.slice(0..index) end #puts seq seq end #Sets the reference file for the gene models def chromosomes(path) @chromosomes_db = Bio::DB::Fasta::FastaFile.new({:fasta=>path}) @chromosomes_path = path end #Retunrs the sequence for a region in the gene models (exon) def chromosome_sequence(region) left_pad = 0 #TODO: Padd if it goes to the right if(region.start < 1) left_pad = region.start * -1 left_pad += 1 region.start = 1 end str = "-" * left_pad << @chromosomes_db.fetch_sequence(region) #str << "n" * (region.size - str.size + 1) if region.size > str.size str end def add_chromosome_arm(opts) @chromosomes = Hash.new unless @chromosomes name = opts[:name] path = opts[:reference_path] path = opts[:alig_path] chromosomes[name] = Bio::DB::Fasta::FastaFile.new({:fasta=>path}) end def add_snp(snp) @snp_map[snp.gene] = Array.new unless @snp_map[snp.gene] @snp_map[snp.gene] << snp end def add_snp_file(filename, chromosome, snp_in, original_name) File.open(filename) do | f | f.each_line do | line | snp = SNP.parse(line) snp.flanking_size = flanking_size if snp.position > 0 snp.container = self snp.chromosome = chromosome snp.snp_in = snp_in snp.original_name = original_name @snp_map[snp.gene] = Array.new unless @snp_map[snp.gene] @snp_map[snp.gene] << snp end end end end def fasta_string_for_snp(snp) gene_region = snp.covered_region local_pos_in_gene = snp.local_position ret_str = "" @parents.each do |name, bam| ret_str << ">#{gene_region.id}_SNP-#{snp.position}_#{name} Overlapping_exons:#{gene_region.to_s} localSNPpo:#{local_pos_in_gene+1}\n" to_print = bam.consensus_with_ambiguities({:region=>gene_region}).to_s to_print[local_pos_in_gene] = to_print[local_pos_in_gene].upcase ret_str << to_print << "\n" end snp.exon_list.each do | chromosome, exon | target_region = exon.target_region exon_start_offset = exon.query_region.start - gene_region.start chr_local_pos=local_pos_in_gene + target_region.start + 1 ret_str << ">#{chromosome}_SNP-#{chr_local_pos} #{exon.to_s} #{target_region.orientation}\n" to_print = "-" * exon_start_offset chr_seq = chromosome_sequence(exon.target_region).to_s l_pos = exon_start_offset + local_pos_in_gene to_print << chr_seq to_print[local_pos_in_gene] = to_print[local_pos_in_gene].upcase ret_str << to_print end ret_str end def print_fasta_snp_exones (file) @missing_exons = Set.new unless @missing_exons @snp_map.each do | gene, snp_array| snp_array.each do |snp| #file.puts snp.primer_fasta_string #puts "In print_fast_np_exones" #puts snp.inspect begin file.puts snp.aligned_sequences_fasta rescue Exception=>e @missing_exons << snp.to_s $stderr.puts "print_fasta_snp_exones:" + snp.to_s + ":" + e.to_s $stderr.puts "Local position: #{snp.local_position}" $stderr.puts "Local position: #{snp.parental_sequences.to_s}" $stderr.puts e.backtrace end end end end def print_primer_3_exons (file, target_chromosome , parental ) added = 0 @snp_map.each do | gene, snp_array| snp_array.each do |snp| string = "" begin primer_3_min_seq_length string = snp.primer_3_string( snp.chromosome, parental ) #puts "print_primer_3_exons: #{string.size}" if string.size > 0 file.puts string added += 1 end rescue Exception=>e @missing_exons << snp.to_s # $stderr.puts "" $stderr.puts "print_primer_3_exons: #{e.to_s} : snp.to_s" $stderr.puts e.backtrace end end end return added end def add_alignments(opts=Hash.new) opts = { :min_identity=>90 }.merge!(opts) exonerate_filename = opts[:exonerate_file] arm_selection = opts[:arm_selection] unless arm_selection arm_selection = lambda do | contig_name | ret = contig_name[0,3] return ret end end File.open(exonerate_filename) do |f| f.each_line do | line | record = Bio::DB::Exonerate::Alignment.parse_custom(line) if record and record.identity >= opts[:min_identity] snp_array = @snp_map[record.query_id] if snp_array != nil snp_array.each do |snp| if snp != nil and snp.position.between?( (record.query_start + 1) , record.query_end) begin exon = record.exon_on_gene_position(snp.position) snp.add_exon(exon, arm_selection.call(record.target_id)) rescue Bio::DB::Exonerate::ExonerateException $stderr.puts "Failed for the range #{record.query_start}-#{record.query_end} for position #{snp.position}" end end end end end end end end def add_parental(opts=Hash.new) # opts = { :name=>opts[:path]}.merge!(opts) sam = nil name = opts[:name] ? opts[:name] : "Unknown" if opts[:path] path = opts[:path] name = opts[:name] ? opts[:name] : path.basename(".bam") sam = Bio::DB::Sam.new({:fasta=>@gene_models_path, :bam=>opts[:path]}) end @parents[name] = sam end end end