Пример #1
0
boolean show_output(void)
{
  int i;

  cDNA * cdna;
  Protein * trans;
  GenomicOverlapResults * gor;
  AlnColumn * alt;
  

 

  if( show_pretty == TRUE ) {
    show_pretty_aln();
  }

  if( show_match_sum == TRUE ) {
    show_MatchSummary_genewise_header(ofp);
    show_MatchSummarySet_genewise(mss,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_pretty_gene == TRUE ) {
    show_pretty_GenomicRegion(gr,0,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_supp_gene == TRUE ) {
    show_pretty_GenomicRegion(gr,1,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_embl == TRUE ) {
    write_Embl_FT_GenomicRegion(gr,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_diana == TRUE ) {
    write_Diana_FT_GenomicRegion(gr,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_overlap == TRUE ) {
    gor = Genomic_overlap(gr,embl);
    show_GenomicOverlapResults(gor,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }


  if( show_trans == TRUE ) {
    for(i=0;i<gr->len;i++) {
      if( gr->gene[i]->ispseudo == TRUE ) {
	fprintf(ofp,"#Gene %d is a pseudo gene - no translation possible\n",i);
      } else {
	trans = get_Protein_from_Translation(gr->gene[i]->transcript[0]->translation[0],ct);
	write_fasta_Sequence(trans->baseseq,ofp);
      }
    } 
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_pep == TRUE ) {
    alt = alb->start;
    for(;alt != NULL;) {
      trans = Protein_from_GeneWise_AlnColumn(gen->baseseq,alt,1,&alt,ct,is_random_AlnColumn_genewise);
      if ( trans == NULL ) 
	break;
      write_fasta_Sequence(trans->baseseq,ofp);
      free_Protein(trans);
    }
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_cdna == TRUE ) {
    for(i=0;i<gr->len;i++) {
      cdna = get_cDNA_from_Transcript(gr->gene[i]->transcript[0]);
      write_fasta_Sequence(cdna->baseseq,ofp);
    } 
    fprintf(ofp,"%s\n",divide_str);
  }


  if( show_ace == TRUE ) {
    show_ace_GenomicRegion(gr,gen->baseseq->name,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_gff == TRUE ) {
    show_GFF_GenomicRegion(gr,gen->baseseq->name,"GeneWise",ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_gene_plain == TRUE ) {
    show_GenomicRegion(gr,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_AlnBlock == TRUE ) {
    mapped_ascii_AlnBlock(alb,Score2Bits,0,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_cumlative_PackAln == TRUE ) {
    show_bits_and_cumlative_PackAln(pal,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }

  if( show_PackAln == TRUE ) {
    show_simple_PackAln(pal,ofp);
    fprintf(ofp,"%s\n",divide_str);
  }
  


  return TRUE;
}
Пример #2
0
boolean show_output(void)
{
  int i,k;
  ThreeStateModel * temptsm;
  AlnBlock * alb;
  PackAln * pal;
  MatchSummarySet * mss;
  Protein * ps;
  cDNA * cdna;
  double bits;
  boolean fitted_res = FALSE;
  AlnBlockList * alist;
  AlnBlock * anchored;
  SequenceSet * set;
  AlnColumn * alt;
  Protein * trans;

  /* sort by bit score first */

  sort_Hscore_by_score(hs);

  if( search_mode == PC_SEARCH_S2DB ) {
    if( hs->his == NULL || hs->his->total < 1000 ) {
	info("Cannot fit histogram to a db smaller than 1,000");
	fprintf(ofp,"[Warning: Can't fit histogram to a db smaller than 1,000]\n\n");
	show_histogram = FALSE;
    } else {
      fitted_res = TRUE;
      fit_Hscore_to_EVD(hs,20);
    }
  }

  /* deal with initialising anchored alignment.
   * Could be done for either single HMMs or single proteins,
   * but we will only do it for HMMs at the moment
   */

  if( make_anchored_aln == TRUE ) {
    if( tsm == NULL ) {
      warn("Attempting to make an achored alignment without a HMM. impossible!");
      make_anchored_aln = FALSE;
    } else {
      anchored = single_unit_AlnBlock(tsm->len,"MATCH_STATE");
      set = SequenceSet_alloc_std();
   }
  }

  /* dofus catcher */
  if( aln_alg != alg ) {
    fprintf(ofp,"\n#\n#WARNING!\n#\n# Your alignment algorithm is different from your search algorithm.\n# This is probably quite sensible but will lead to differing scores.\n# Use the search score as an indicator of the significance of the match\n# Read the docs for more information\n#\n");
  }

  fprintf(ofp,"\n\n#High Score list\n");
  fprintf(ofp,"#Protein ID                 DNA Str  ID                        Bits Evalue\n");  
  fprintf(ofp,"--------------------------------------------------------------------------\n");

  for(i=0;i<hs->len;i++) {
    bits = Score2Bits(hs->ds[i]->score);
    if( bits < search_cutoff ) {
      break;
    }

    if( fitted_res == TRUE && evalue_search_str != NULL ) {
      if( hs->ds[i]->evalue > evalue_search_cutoff ) 
	break;
    }

    if( fitted_res == TRUE) 
      fprintf(ofp,"Protein %-20sDNA [%c] %-24s %.2f %.2g\n",hs->ds[i]->query->name,hs->ds[i]->target->is_reversed == TRUE ? '-' : '+',hs->ds[i]->target->name,bits,hs->ds[i]->evalue);
    else
      fprintf(ofp,"Protein %-20sDNA [%c] %-24s %.2f\n",hs->ds[i]->query->name,hs->ds[i]->target->is_reversed == TRUE ? '-' : '+',hs->ds[i]->target->name,bits);

  }

  if( search_mode == PC_SEARCH_S2DB && show_histogram == TRUE ) {
    fprintf(ofp,"\n\n#Histogram\n");
    fprintf(ofp,"-----------------------------------------------------------------------\n");
    PrintASCIIHistogram(hs->his,ofp);
  }

  fprintf(ofp,"\n\n#Alignments\n");
  fprintf(ofp,"-----------------------------------------------------------------------\n");

  for(i=0;i<hs->len;i++) {
    bits = Score2Bits(hs->ds[i]->score);
    if( bits < search_cutoff ) {
      break;
    }
    if( i >= aln_number ) {
      break;
    }

    if( fitted_res == TRUE && evalue_search_str != NULL ) {
      if( hs->ds[i]->evalue > evalue_search_cutoff ) 
	break;
    }

    
    fprintf(ofp,"\n\n>Results for %s vs %s (%s) [%d]\n",hs->ds[i]->query->name,hs->ds[i]->target->name,hs->ds[i]->target->is_reversed == TRUE ? "reverse" : "forward",i+1 );

    cdna = get_cDNA_from_cDNADB(cdb,hs->ds[i]->target);
    temptsm = indexed_ThreeStateModel_ThreeStateDB(tsmdb,hs->ds[i]->query);


    alb = AlnBlock_from_TSM_estwise_wrap(temptsm,cdna,cps,cm,ct,rmd,aln_alg,use_syn,allN,flat_insert,dpri,&pal);

    if( alb == NULL ) {
      warn("Got a NULL alignment. Exiting now due to presumed problems");
      fprintf(ofp,"\n\n*Got a NULL alignment. Exiting now due to presumed problems*\n\n");
      return FALSE;
    }


 
    if( use_single_pro == FALSE) 
      mss = MatchSummarySet_from_AlnBlock_genewise(alb,temptsm->name,1,cdna->baseseq);
    else
      mss = MatchSummarySet_from_AlnBlock_genewise(alb,pro->baseseq->name,pro->baseseq->offset,cdna->baseseq);

    
    if( show_pretty == TRUE ) {

      fprintf(ofp,"\n%s output\nScore %4.2f bits over entire alignment.\nThis will be different from per-alignment scores. See manual for details\nFor computer parsable output, try %s -help or read the manual\n",program_name,Score2Bits(pal->score),program_name);
      
      if( use_syn == FALSE ) {
	fprintf(ofp,"Scores as bits over a flat simple random model\n\n");
      } else {
	fprintf(ofp,"Scores as bits over a synchronous coding model\n\n");
      }
      
      ps = pseudo_Protein_from_ThreeStateModel(temptsm);
      protcdna_ascii_display(alb,ps->baseseq->seq,ps->baseseq->name,ps->baseseq->offset,cdna,ct,15,main_block,TRUE,ofp);

      
      free_Protein(ps);

      fprintf(ofp,"%s\n",divide_str);
      
    }

    if( show_match_sum == TRUE ) {
      show_MatchSummary_genewise_header(ofp);
      show_MatchSummarySet_genewise(mss,ofp);
      fprintf(ofp,"%s\n",divide_str);
    }
    

    if( show_pep == TRUE ) {
      alt = alb->start;
      for(;alt != NULL;) {
	trans = Protein_from_GeneWise_AlnColumn(cdna->baseseq,alt,1,&alt,ct,is_random_AlnColumn_genewise);
	if ( trans == NULL ) 
	  break;
	write_fasta_Sequence(trans->baseseq,ofp);
	free_Protein(trans);
      }
      fprintf(ofp,"%s\n",divide_str);
    }

    if( show_AlnBlock == TRUE ) {
      mapped_ascii_AlnBlock(alb,Score2Bits,0,ofp);
      fprintf(ofp,"%s\n",divide_str);
    }
    
    if( show_PackAln == TRUE ) {
      show_simple_PackAln(pal,ofp);
      fprintf(ofp,"%s\n",divide_str);
    }

    /*
     * This goes at the end because it destroys the alb structure
     */

    if( make_anchored_aln == TRUE ) {
      /* attach sequence to als in alb, so we have it for later use */
      alb->seq[1]->data = (void *) cdna->baseseq;
      /* add to SequenceSet so we can destroy the memory */
      add_SequenceSet(set,hard_link_Sequence(cdna->baseseq));

      alist = split_AlnBlock(alb,is_random_AlnColumn_genewise);

      for(k=0;k<alist->len;k++) {
	/* actually produce the anchored alignment */
	/*mapped_ascii_AlnBlock(alist->alb[k],Score2Bits,stderr);*/
	add_to_anchored_AlnBlock(anchored,alist->alb[k]);

	/*	dump_ascii_AlnBlock(anchored,stderr);*/
      }
    }

    alb = free_AlnBlock(alb);
    pal = free_PackAln(pal);
    mss = free_MatchSummarySet(mss);
    cdna = free_cDNA(cdna);
    temptsm = free_ThreeStateModel(temptsm);

  }

  if( do_complete_analysis == TRUE ) {
    fprintf(ofp,"\n\n#Complete Analysis\n");
    fprintf(ofp,"-------------------------------------------------------------\n\n");
    
    /* ok - end of loop over relevant hits. If we have an
     * anchored alignment, print it out!
     */
    if( make_anchored_aln == TRUE ) {
      /*dump_ascii_AlnBlock(anchored,stderr);*/
      write_mul_estwise_AlnBlock(anchored,ct,ofp);
      fprintf(ofp,"%s\n",divide_str);
    }
  }


  return TRUE;
}