Esempio n. 1
0
  /** Get the simplest string describing the effect (this is mostly used for testcases) */
  public String toStringSimple(boolean shortFormat) {
    String transcriptId = "";
    Transcript tr = getTranscript();
    if (tr != null) transcriptId = tr.getId();

    String exonId = "";
    Exon exon = getExon();
    if (exon != null) exonId = exon.getId();

    String eff = effect(shortFormat, true, true, false);
    if (!eff.isEmpty()) return eff;
    if (!exonId.isEmpty()) return exonId;
    if (!transcriptId.isEmpty()) return transcriptId;

    return "NO EFFECT";
  }
Esempio n. 2
0
  public String toString(boolean useSeqOntology, boolean useHgvs) {
    // Get data to show
    String geneId = "", geneName = "", bioType = "", transcriptId = "", exonId = "", customId = "";
    int exonRank = -1;

    if (marker != null) {
      // Gene Id, name and biotype
      Gene gene = getGene();
      Transcript tr = getTranscript();

      // CDS size info
      if (gene != null) {
        geneId = gene.getId();
        geneName = gene.getGeneName();
        bioType = getBiotype();
      }

      // Update trId
      if (tr != null) transcriptId = tr.getId();

      // Exon rank information
      Exon exon = getExon();
      if (exon != null) {
        exonId = exon.getId();
        exonRank = exon.getRank();
      }

      // Regulation
      if (isRegulation()) bioType = ((Regulation) marker).getCellType();
    }

    // Add seqChage's ID
    if (!variant.getId().isEmpty()) customId += variant.getId();

    // Add custom markers
    if ((marker != null) && (marker instanceof Custom))
      customId += (customId.isEmpty() ? "" : ";") + marker.getId();

    // CDS length
    int cdsSize = getCdsLength();

    String errWarn = error + (error.isEmpty() ? "" : "|") + warning;

    String aaChange = "";
    if (useHgvs) aaChange = getHgvs();
    else aaChange = ((aaRef.length() + aaAlt.length()) > 0 ? aaRef + "/" + aaAlt : "");

    return errWarn //
        + "\t"
        + geneId //
        + "\t"
        + geneName //
        + "\t"
        + bioType //
        + "\t"
        + transcriptId //
        + "\t"
        + exonId //
        + "\t"
        + (exonRank >= 0 ? exonRank : "") //
        + "\t"
        + effect(false, false, false, useSeqOntology) //
        + "\t"
        + aaChange //
        + "\t"
        + ((codonsRef.length() + codonsAlt.length()) > 0 ? codonsRef + "/" + codonsAlt : "") //
        + "\t"
        + (codonNum >= 0 ? (codonNum + 1) : "") //
        + "\t"
        + (codonDegeneracy >= 0 ? codonDegeneracy + "" : "") //
        + "\t"
        + (cdsSize >= 0 ? cdsSize : "") //
        + "\t"
        + (codonsAroundOld.length() > 0 ? codonsAroundOld + " / " + codonsAroundNew : "") //
        + "\t"
        + (aasAroundOld.length() > 0 ? aasAroundOld + " / " + aasAroundNew : "") //
        + "\t"
        + customId //
    ;
  }