<?xml version="1.0" encoding="UTF-8"?>
<RUN_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <RUN alias="342103a821a035946f9bd6a4d5e62f96" center_name="University of Washington Genome Sciences" broker_name="UM-SPH" run_center="University of Washington Genome Sciences" accession="SRR3123703">
    <IDENTIFIERS>
      <PRIMARY_ID>SRR3123703</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Washington Genome Sciences">342103a821a035946f9bd6a4d5e62f96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Secondary mapping Build 37 for NWD350175 [17675]</TITLE>
    <EXPERIMENT_REF accession="SRX1544737" refname="NWD350175-expt" refcenter="University of Washington Genome Sciences"/>
    <PROCESSING>
      <PIPELINE>
        <PIPE_SECTION section_name="read mapping">
          <STEP_INDEX> none </STEP_INDEX>
          <PREV_STEP_INDEX>NIL</PREV_STEP_INDEX>
          <PROGRAM> bwa mem </PROGRAM>
          <VERSION> 0.7.10-r789 </VERSION>
          <NOTES/>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="sort / merge / mark duplicates">
          <STEP_INDEX> new </STEP_INDEX>
          <PREV_STEP_INDEX> none </PREV_STEP_INDEX>
          <PROGRAM> Picard </PROGRAM>
          <VERSION> 1.111 </VERSION>
          <NOTES/>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="realign around indels">
          <STEP_INDEX> yes </STEP_INDEX>
          <PREV_STEP_INDEX> new </PREV_STEP_INDEX>
          <PROGRAM> GATK IndelRealigner </PROGRAM>
          <VERSION> 3.2-2 </VERSION>
          <NOTES> knownAlleles = dbSNP138.vcf, targetIntervals = sample-specific </NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="recalibrate base call quality scores">
          <STEP_INDEX> old </STEP_INDEX>
          <PREV_STEP_INDEX> yes </PREV_STEP_INDEX>
          <PROGRAM> GATK BaseRecalibrator </PROGRAM>
          <VERSION> 3.2-2 </VERSION>
          <NOTES> [ ReadGroupCovariate, QualityScoreCovariate, CycleCovariate, DinucCovariate ] </NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="compress base call quality scores">
          <STEP_INDEX> done </STEP_INDEX>
          <PREV_STEP_INDEX> old </PREV_STEP_INDEX>
          <PROGRAM> bamUtils squeeze </PROGRAM>
          <VERSION> 1.0.13 </VERSION>
          <NOTES> --keepDups  --binMid  --binQualS 2,3,10,20,25,30,35,40,50  </NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="convert to .cram format">
          <STEP_INDEX> home </STEP_INDEX>
          <PREV_STEP_INDEX> done </PREV_STEP_INDEX>
          <PROGRAM> samtools view -C </PROGRAM>
          <VERSION> 1.2 Using htslib 1.2.1 </VERSION>
          <NOTES> genome reference sequence retrieved from:  ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/technical/reference/phase2_reference_assembly_sequence/hs37d5.fa.gz </NOTES>
        </PIPE_SECTION>
      </PIPELINE>
    </PROCESSING>
    <RUN_ATTRIBUTES>
      <RUN_ATTRIBUTE>
        <TAG>assembly</TAG>
        <VALUE>GRCh37</VALUE>
      </RUN_ATTRIBUTE>
      <RUN_ATTRIBUTE>
        <TAG>Alignment Provider</TAG>
        <VALUE>Sequencing Center</VALUE>
      </RUN_ATTRIBUTE>
    </RUN_ATTRIBUTES>
  </RUN>
</RUN_SET>
