Modified comments.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3158 348d0f76-0448-11de-a6fe-93d51630548a
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package org.broadinstitute.sting.playground.gatk.walkers.annotator;
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package org.broadinstitute.sting.playground.gatk.walkers.annotator;
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import java.io.File;
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import java.util.Collection;
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@ -31,40 +31,10 @@ import org.broadinstitute.sting.utils.genotype.vcf.VCFHeaderLine;
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import org.broadinstitute.sting.utils.genotype.vcf.VCFUtils;
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import org.broadinstitute.sting.utils.genotype.vcf.VCFWriter;
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/*
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General documentation - todo put this in wiki?
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The GenomicAnnotator
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Input Files:
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- Input files are specified using the -B<name>,<type>,<file path> arg.
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- One of the -B args should have the <name> "variants" and contain the genotypes to be annotated.
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- Data files are also provided using the -B arg and should have <type> be "table".
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Table format:
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- the coordinates must be position-based rather than offset-based (eg. 1-based half-open)
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- special rows:
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- can contain comment lines starting with #
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- at the top of the file, there must be a header line of the form:
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HEADER columnName1 columnName2 etc. TODO finalize this
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- special columns:
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- first column must be of the form chr:pos or chr:start-end.
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- alt/ref haplotypes:
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- if there is a column named "hap_ref", a variant will only be annotated with a given row if that row's "hap_ref" allele exactly matches the variant's reference sequence.
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-
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*/
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/**
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* Annotates variant calls with context information. Users can specify which of the available annotations to use.
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* Annotates variant calls with information from user-provided tabular files.
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* See: {TODO: put wiki url}
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*/
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//@Requires(value={DataSource.READS, DataSource.REFERENCE},referenceMetaData=@RMD(name="variant",type=VariationRod.class))
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@Allows(value={DataSource.READS, DataSource.REFERENCE})
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