Modified comments.

git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3158 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
weisburd 2010-04-13 15:41:59 +00:00
parent 7b05091c04
commit d0123956bc
1 changed files with 3 additions and 33 deletions

View File

@ -1,4 +1,4 @@
package org.broadinstitute.sting.playground.gatk.walkers.annotator;
package org.broadinstitute.sting.playground.gatk.walkers.annotator;
import java.io.File;
import java.util.Collection;
@ -31,40 +31,10 @@ import org.broadinstitute.sting.utils.genotype.vcf.VCFHeaderLine;
import org.broadinstitute.sting.utils.genotype.vcf.VCFUtils;
import org.broadinstitute.sting.utils.genotype.vcf.VCFWriter;
/*
General documentation - todo put this in wiki?
The GenomicAnnotator
Input Files:
- Input files are specified using the -B<name>,<type>,<file path> arg.
- One of the -B args should have the <name> "variants" and contain the genotypes to be annotated.
- Data files are also provided using the -B arg and should have <type> be "table".
Table format:
- the coordinates must be position-based rather than offset-based (eg. 1-based half-open)
- special rows:
- can contain comment lines starting with #
- at the top of the file, there must be a header line of the form:
HEADER columnName1 columnName2 etc. TODO finalize this
- special columns:
- first column must be of the form chr:pos or chr:start-end.
- alt/ref haplotypes:
- 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.
-
*/
/**
* Annotates variant calls with context information. Users can specify which of the available annotations to use.
* Annotates variant calls with information from user-provided tabular files.
* See: {TODO: put wiki url}
*/
//@Requires(value={DataSource.READS, DataSource.REFERENCE},referenceMetaData=@RMD(name="variant",type=VariationRod.class))
@Allows(value={DataSource.READS, DataSource.REFERENCE})