Check for bad reference bases before creating simple/'empty' VCs. Updated the code in the indel GL model to be consistent and to use the existing utility in the Allele class.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@5704 348d0f76-0448-11de-a6fe-93d51630548a
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@ -231,23 +231,15 @@ public class IndelGenotypeLikelihoodsCalculationModel extends GenotypeLikelihood
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//System.out.println(new String(ref.getBases()));
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byte[] refBases = Arrays.copyOfRange(ref.getBases(),startIdxInReference,startIdxInReference+dLen);
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boolean ok = true;
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for (int i=0; i < refBases.length; i++)
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if (!BaseUtils.isRegularBase(refBases[i]))
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ok = false;
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if (ok) {
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if (Allele.acceptableAlleleBases(refBases)) {
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refAllele = Allele.create(refBases,true);
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altAllele = Allele.create(Allele.NULL_ALLELE_STRING, false);
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}
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}
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else {
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// insertion case
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boolean ok = true;
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for (int i=0; i < bestAltAllele.length(); i++)
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if (!BaseUtils.isRegularBase(bestAltAllele.getBytes()[i]))
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ok = false;
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if (ok) {
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if (Allele.acceptableAlleleBases(bestAltAllele)) {
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refAllele = Allele.create(Allele.NULL_ALLELE_STRING, true);
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altAllele = Allele.create(bestAltAllele, false);
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}
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@ -203,6 +203,10 @@ public class UnifiedGenotyperEngine {
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return null;
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vc = new VariantContext("UG_call", vcInput.getChr(), vcInput.getStart(), vcInput.getEnd(), vcInput.getAlleles());
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} else {
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// deal with bad/non-standard reference bases
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if ( !Allele.acceptableAlleleBases(new byte[]{ref.getBase()}) )
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return null;
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Set<Allele> alleles = new HashSet<Allele>();
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alleles.add(Allele.create(ref.getBase(), true));
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vc = new VariantContext("UG_call", ref.getLocus().getContig(), ref.getLocus().getStart(), ref.getLocus().getStart(), alleles);
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