Documentation for more basic walkers.
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@ -36,7 +36,9 @@ import net.sf.samtools.SAMReadGroupRecord;
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import java.util.*;
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/**
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* Display the depth of coverage at a given locus.
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* Computes the depth of coverage at all loci in the specified region of the reference. Includes features to control
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* grouping of results by read group or by sample, or filtering loci with either a small number of overlapping alignments
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* or with alignments of poor mapping quality. Can optionally include individual base counts at each locus.
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*/
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@By(DataSource.REFERENCE)
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public class DepthOfCoverageWalker extends LocusWalker<DepthOfCoverageWalker.DoCInfo, DepthOfCoverageWalker.DoCInfo> {
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@ -8,8 +8,10 @@ import net.sf.samtools.SAMRecord;
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import java.io.*;
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// create a fastq file from a bam file
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/**
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* Converts reads from the input BAM file into fastq format, stripping away all alignment information.
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* Optionally re-reverses the negative strand alignments using the --re-reverse command-line argument.
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*/
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@WalkerName("BamToFastq")
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public class BamToFastqWalker extends ReadWalker<Integer, Integer> {
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@ -10,8 +10,10 @@ import org.broadinstitute.sting.utils.GenomeLocParser;
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import org.broadinstitute.sting.utils.Pair;
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import org.broadinstitute.sting.utils.cmdLine.Argument;
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// create a fasta sequence file from a reference and intervals
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/**
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* Renders a new reference in FASTA format consisting of only those loci provided in the input data set. Has optional
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* features to control the output format.
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*/
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@WalkerName("FastaReferenceMaker")
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public class FastaReferenceWalker extends RefWalker<Pair<GenomeLoc, String>, GenomeLoc> {
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@Argument(fullName="lineWidth", shortName="lw", doc="Maximum length of sequence to write per line", required=false) public int fastaLineWidth=60;
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