removing some unused code.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3121 348d0f76-0448-11de-a6fe-93d51630548a
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package org.broadinstitute.sting.utils.genotype;
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/**
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* @author ebanks
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* <p/>
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* Class GenotypeCall
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* <p/>
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* represents the genotype-specific data associated with a genotype call.
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*/
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public interface GenotypeCall extends Genotype {
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/**
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*
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* @param variation the Variation object associated with this genotype
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*/
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public void setVariation(Variation variation);
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/**
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*
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* @param genotype the genotype
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*/
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public void setGenotype(DiploidGenotype genotype);
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/**
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*
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* @param value -log10PEror
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*/
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public void setNegLog10PError(double value);
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}
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package org.broadinstitute.sting.utils.genotype;
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import org.broadinstitute.sting.utils.pileup.ReadBackedPileup;
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/**
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* @author ebanks
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*
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* Interface ReadBacked
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*
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* This interface indicates that a genotype or variant is backed by reads
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*/
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public interface ReadBacked {
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/**
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* get the pileup that backs this genotype call
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* @return a pileup
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*/
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public ReadBackedPileup getPileup();
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/**
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*
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* @param pileup the pileup for this genotype
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*/
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public void setPileup(ReadBackedPileup pileup);
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/**
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* get the count of reads
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* @return the number of reads we're backed by
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*/
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public int getReadCount();
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}
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package org.broadinstitute.sting.utils.genotype;
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import java.util.List;
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/**
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* @author ebanks
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* <p/>
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* Class VariationCall
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* <p/>
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* represents locus specific (non-genotype) data associated with a call plus the ability to set genotypes.
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*/
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public interface VariationCall extends Variation {
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/**
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*
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* @param alt the alternate allele base for this variation
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*/
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public void addAlternateAllele(String alt);
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/**
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*
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* @return true if the allele frequency has been set
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*/
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public boolean hasNonRefAlleleFrequency();
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/**
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*
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* @param frequency the allele frequency for this variation
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*/
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public void setNonRefAlleleFrequency(double frequency);
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/**
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*
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* @param calls the Genotypes for this variation
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*/
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public void setGenotypeCalls(List<Genotype> calls);
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}
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