<?xml version="1.0" encoding="UTF-8"?>
<RUN_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <RUN accession="SRR3082797" alias="140722_SN898_0576_BC4GF8ACXX_1_ID03">
    <IDENTIFIERS>
      <PRIMARY_ID>SRR3082797</PRIMARY_ID>
      <SUBMITTER_ID namespace="BCM">140722_SN898_0576_BC4GF8ACXX_1_ID03</SUBMITTER_ID>
    </IDENTIFIERS>
    <EXPERIMENT_REF accession="SRX1514625">
      <IDENTIFIERS>
        <SUBMITTER_ID namespace="BCM">PAMPC3.TUD-CC-757-N-1_1AMP-6</SUBMITTER_ID>
      </IDENTIFIERS>
    </EXPERIMENT_REF>
    <PROCESSING>
      <PIPELINE>
        <PIPE_SECTION section_name="Mapping_1">
          <STEP_INDEX>1</STEP_INDEX>
          <PREV_STEP_INDEX>NIL</PREV_STEP_INDEX>
          <PROGRAM>bwa</PROGRAM>
          <VERSION>0.6.2</VERSION>
          <NOTES>bwa aln reference.fasta 1.fastq &gt; fastq.sai (repeated for the pair)</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="Mapping_2">
          <STEP_INDEX>2</STEP_INDEX>
          <PREV_STEP_INDEX>1</PREV_STEP_INDEX>
          <PROGRAM>bwa</PROGRAM>
          <VERSION>0.6.2</VERSION>
          <NOTES>bwa sampe reference.fasta fastq1.sai fastq2.sai &gt; barcode.sam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MarkDuplicates">
          <STEP_INDEX>4</STEP_INDEX>
          <PREV_STEP_INDEX>3</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.93</VERSION>
          <NOTES>java -jar MarkDuplicates.jar I=barcode.sorted.bam O=barcode.marked.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="IndelRealigner">
          <STEP_INDEX>7</STEP_INDEX>
          <PREV_STEP_INDEX>6</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T IndelRealigner -I barcode.marked.bam -R reference.fasta -targetIntervals barcode.intervals --downsampling_type NONE --consensusDeterminationModel USE_READS -known 1000G_phase1.indels.b37.vcf.gz -known Mills_and_1000G_gold_standard.indels.b37.vcf.gz -o barcode_realigned.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="PrintReads">
          <STEP_INDEX>9</STEP_INDEX>
          <PREV_STEP_INDEX>8</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T PrintReads -I barcode_realigned.bam -R reference.fasta -BQSR barcode.GATKrecal_data.grp --emit_original_quals --downsampling_type NONE -o barcode_recal.realigned.bam</NOTES>
        </PIPE_SECTION>
      </PIPELINE>
    </PROCESSING>
  </RUN>
</RUN_SET>
