trivial code restructuing, and commented out failed attempt to support sample selection with VCF. VariantEval2 go go go
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@2516 348d0f76-0448-11de-a6fe-93d51630548a
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@ -6,8 +6,11 @@ import org.broadinstitute.sting.gatk.walkers.*;
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import org.broadinstitute.sting.gatk.refdata.*;
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import org.broadinstitute.sting.utils.StingException;
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import org.broadinstitute.sting.utils.Utils;
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import org.broadinstitute.sting.utils.GenomeLoc;
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import org.broadinstitute.sting.utils.cmdLine.Argument;
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import org.broadinstitute.sting.utils.genotype.Variation;
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import org.broadinstitute.sting.utils.genotype.Genotype;
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import org.broadinstitute.sting.utils.genotype.BasicGenotype;
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import java.io.File;
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import java.io.FileNotFoundException;
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@ -55,6 +58,9 @@ public class VariantEvalWalker extends RodWalker<Integer, Integer> {
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@Argument(fullName = "samplesFile", shortName="samples", doc="When running an analysis on one or more individuals with truth data, this field provides a filepath to the listing of which samples are used (and are used to name corresponding rods with -B)", required=false)
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public String samplesFile = null;
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@Argument(fullName = "sampleName", shortName="sampleName", doc="When running an analysis on one or more individuals with truth data, provide this parameter to only analyze the genotype of this sample", required=false)
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public String sampleName = null;
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String analysisFilenameBase = null;
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final String knownSNPDBName = "dbSNP";
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@ -248,8 +254,24 @@ public class VariantEvalWalker extends RodWalker<Integer, Integer> {
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if (eval != null)
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if (eval.getNegLog10PError() * 10.0 < minConfidenceScore) eval = null;
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if ( eval != null && (eval instanceof RodVCF) && ((RodVCF)eval).mCurrentRecord.isFiltered() ) {
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if ( ! includeFilteredRecords ) eval = null; // we are not including filtered records, so set eval to null
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if ( eval != null && (eval instanceof RodVCF) ) {
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if ( ((RodVCF)eval).mCurrentRecord.isFiltered() && ! includeFilteredRecords ) {
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//System.out.printf("Rejecting filtered record %s%n", eval);
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eval = null; // we are not including filtered records, so set eval to null
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}
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// } else if ( sampleName != null ) {
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// // code to grab a particular sample from a VCF
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// Variation evalOld = eval;
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// Genotype evalG = ((RodVCF)evalOld).getGenotype(sampleName);
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// if ( evalG == null ) throw new StingException("Unexpected null genotype for sample " + sampleName);
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// BasicGenotype g = new BasicGenotype(evalG.getLocation(), evalG.getBases(), ref.getBase(), evalG.getNegLog10PError());
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// if ( g.isVariant(ref.getBase()) ) {
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// eval = g.toVariation(ref.getBase());
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// System.out.printf("Replacing %s with %s%n", evalOld, eval);
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// } else {
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// eval = null;
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// }
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// }
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}
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// update stats about all of the SNPs
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