removing some unused code.

git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3121 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
aaron 2010-04-05 19:30:08 +00:00
parent 56eb15f91f
commit df7e7921ce
3 changed files with 0 additions and 100 deletions

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@ -1,31 +0,0 @@
package org.broadinstitute.sting.utils.genotype;
/**
* @author ebanks
* <p/>
* Class GenotypeCall
* <p/>
* represents the genotype-specific data associated with a genotype call.
*/
public interface GenotypeCall extends Genotype {
/**
*
* @param variation the Variation object associated with this genotype
*/
public void setVariation(Variation variation);
/**
*
* @param genotype the genotype
*/
public void setGenotype(DiploidGenotype genotype);
/**
*
* @param value -log10PEror
*/
public void setNegLog10PError(double value);
}

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@ -1,30 +0,0 @@
package org.broadinstitute.sting.utils.genotype;
import org.broadinstitute.sting.utils.pileup.ReadBackedPileup;
/**
* @author ebanks
*
* Interface ReadBacked
*
* This interface indicates that a genotype or variant is backed by reads
*/
public interface ReadBacked {
/**
* get the pileup that backs this genotype call
* @return a pileup
*/
public ReadBackedPileup getPileup();
/**
*
* @param pileup the pileup for this genotype
*/
public void setPileup(ReadBackedPileup pileup);
/**
* get the count of reads
* @return the number of reads we're backed by
*/
public int getReadCount();
}

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@ -1,39 +0,0 @@
package org.broadinstitute.sting.utils.genotype;
import java.util.List;
/**
* @author ebanks
* <p/>
* Class VariationCall
* <p/>
* represents locus specific (non-genotype) data associated with a call plus the ability to set genotypes.
*/
public interface VariationCall extends Variation {
/**
*
* @param alt the alternate allele base for this variation
*/
public void addAlternateAllele(String alt);
/**
*
* @return true if the allele frequency has been set
*/
public boolean hasNonRefAlleleFrequency();
/**
*
* @param frequency the allele frequency for this variation
*/
public void setNonRefAlleleFrequency(double frequency);
/**
*
* @param calls the Genotypes for this variation
*/
public void setGenotypeCalls(List<Genotype> calls);
}