Documentation for more basic walkers.

git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@2329 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
hanna 2009-12-11 18:15:40 +00:00
parent d1815f3559
commit 590aeee7d2
3 changed files with 11 additions and 5 deletions

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@ -36,7 +36,9 @@ import net.sf.samtools.SAMReadGroupRecord;
import java.util.*;
/**
* Display the depth of coverage at a given locus.
* Computes the depth of coverage at all loci in the specified region of the reference. Includes features to control
* grouping of results by read group or by sample, or filtering loci with either a small number of overlapping alignments
* or with alignments of poor mapping quality. Can optionally include individual base counts at each locus.
*/
@By(DataSource.REFERENCE)
public class DepthOfCoverageWalker extends LocusWalker<DepthOfCoverageWalker.DoCInfo, DepthOfCoverageWalker.DoCInfo> {

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@ -8,8 +8,10 @@ import net.sf.samtools.SAMRecord;
import java.io.*;
// create a fastq file from a bam file
/**
* Converts reads from the input BAM file into fastq format, stripping away all alignment information.
* Optionally re-reverses the negative strand alignments using the --re-reverse command-line argument.
*/
@WalkerName("BamToFastq")
public class BamToFastqWalker extends ReadWalker<Integer, Integer> {

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@ -10,8 +10,10 @@ import org.broadinstitute.sting.utils.GenomeLocParser;
import org.broadinstitute.sting.utils.Pair;
import org.broadinstitute.sting.utils.cmdLine.Argument;
// create a fasta sequence file from a reference and intervals
/**
* Renders a new reference in FASTA format consisting of only those loci provided in the input data set. Has optional
* features to control the output format.
*/
@WalkerName("FastaReferenceMaker")
public class FastaReferenceWalker extends RefWalker<Pair<GenomeLoc, String>, GenomeLoc> {
@Argument(fullName="lineWidth", shortName="lw", doc="Maximum length of sequence to write per line", required=false) public int fastaLineWidth=60;