remove FixBAMSortOrder walker.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3830 348d0f76-0448-11de-a6fe-93d51630548a
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/*
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* Copyright (c) 2010 The Broad Institute
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*
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* Permission is hereby granted, free of charge, to any person
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* obtaining a copy of this software and associated documentation
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* files (the "Software"), to deal in the Software without
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* restriction, including without limitation the rights to use,
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* copy, modify, merge, publish, distribute, sublicense, and/or sell
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* copies of the Software, and to permit persons to whom the
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* Software is furnished to do so, subject to the following
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* conditions:
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*
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* The above copyright notice and this permission notice shall be
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* included in all copies or substantial portions of the Software.
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*
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* THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND,
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* EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES
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* OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND
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* NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT
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* HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER LIABILITY,
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* WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING
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* FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR
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* THE USE OR OTHER DEALINGS IN THE SOFTWARE.
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*/
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package org.broadinstitute.sting.gatk.walkers;
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/* Motivation: BAM files created by samtools which are sorted often don't
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* have the sort order set to 'coordinate' in the BAM header (instead it's
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* marked as 'unsorted'. Because BAMs are binary files, there's no way to
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* easily change the tag.
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*
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* This walker rewrites a BAM file so that the output is identical to the input
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* except that the sort order tag is set to 'coordinate'.
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*
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* Important note: to run properly in the GATK, the '-U' flag must be used so that
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* the input BAM file not be rejected by the system.
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*/
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import org.broadinstitute.sting.gatk.GenomeAnalysisEngine;
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import org.broadinstitute.sting.gatk.contexts.ReferenceContext;
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import org.broadinstitute.sting.gatk.refdata.ReadMetaDataTracker;
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import org.broadinstitute.sting.commandline.Argument;
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import net.sf.samtools.SAMFileWriter;
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import net.sf.samtools.SAMRecord;
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import net.sf.samtools.SAMFileHeader;
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import net.sf.samtools.SAMFileWriterFactory;
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import java.io.File;
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/**
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* Fixes slightly corrupted BAM files by rewriting the input BAM file, altering
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* the header by changing the sort order tag (SO) to coordinate sort order. Will NOT
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* verify the contents of the file to ensure that the data is actually in coordinate sorted
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* order.
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*/
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public class FixBAMSortOrderTag extends ReadWalker<SAMRecord, SAMFileWriter> {
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@Argument(required=true, shortName="out_bam", doc="The samfile to output to")
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public File SAM_FILE_OUTPUT_LOCATION;
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@Argument(required=false, shortName="sortorder", doc="the sort order to emit in")
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public SAMFileHeader.SortOrder SORT_ORDER=SAMFileHeader.SortOrder.coordinate;
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@Override
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public SAMRecord map(ReferenceContext ref, SAMRecord read, ReadMetaDataTracker metaDataTracker) {
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return read;
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}
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@Override
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public SAMFileWriter reduceInit() {
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SAMFileHeader header = GenomeAnalysisEngine.instance.getSAMFileHeader();
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header.setSortOrder(SORT_ORDER);
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SAMFileWriterFactory factory = new SAMFileWriterFactory();
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return factory.makeBAMWriter(header,false,SAM_FILE_OUTPUT_LOCATION);
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}
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@Override
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public SAMFileWriter reduce(SAMRecord value, SAMFileWriter sum) {
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sum.addAlignment(value);
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return sum;
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}
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public void onTraversalDone(SAMFileWriter result) {
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result.close();
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}
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}
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