<?xml version="1.0" encoding="UTF-8"?>
<RUN_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <RUN accession="SRR2986953" alias="130216_SN733_0370_AC1N3BACXX_5_ID04">
    <IDENTIFIERS>
      <PRIMARY_ID>SRR2986953</PRIMARY_ID>
      <SUBMITTER_ID namespace="BCM">130216_SN733_0370_AC1N3BACXX_5_ID04</SUBMITTER_ID>
    </IDENTIFIERS>
    <EXPERIMENT_REF accession="SRX1475481">
      <IDENTIFIERS>
        <SUBMITTER_ID namespace="BCM">ARBRMR.A06526-2_1AMP-3</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 $aln_params -t $t $index_base read.txt &gt; read.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 $sampe_params $index_base read1.sai read2.sai</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="FixMateInformation">
          <STEP_INDEX>3</STEP_INDEX>
          <PREV_STEP_INDEX>2</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.88</VERSION>
          <NOTES>java -jar FixMateInformation.jar I=merge.bam O=fix.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MarkDuplicates">
          <STEP_INDEX>4</STEP_INDEX>
          <PREV_STEP_INDEX>3</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.88</VERSION>
          <NOTES>java –jar MarkDuplicates.jar I=fix.bam METRICS_FILE=metrics.txt O=dedup.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="AddOrReplaceReadGroups">
          <STEP_INDEX>5</STEP_INDEX>
          <PREV_STEP_INDEX>4</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.88</VERSION>
          <NOTES>java -jar AddOrReplaceReadGroups.jar $rg I=/dev/stdin O=input-$i.bam VALIDATION_STRINGENCY=SILENT </NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="RealignerTargetCreator">
          <STEP_INDEX>6</STEP_INDEX>
          <PREV_STEP_INDEX>5</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T RealignerTargetCreator -I dedup.bam -R ref.fa -nt $nt $known_indels --downsampling_type NONE -o target.intervals</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 dedup.bam -R ref.fa -targetIntervals target.intervals -o realigned.bam $known_indels --downsampling_type NONE</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="BaseRecalibrator">
          <STEP_INDEX>8</STEP_INDEX>
          <PREV_STEP_INDEX>7</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T BaseRecalibrator -I realigned.bam -R ref.fa -nct $nt $dbsnps $indels --downsampling_type NONE -cov ReadGroupCovariate -cov QualityScoreCovariate -cov CycleCovariate -cov ContextCovariate -o recal_data.grp</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 -BQSR recal_data.grp -R ref.fa -I realigned.bam -nct $nt --downsampling_type NONE --emit_original_quals -o recaled.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergeSamFiles">
          <STEP_INDEX>10</STEP_INDEX>
          <PREV_STEP_INDEX>9</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.88</VERSION>
          <NOTES>java -jar MergeSamFiles.jar I=barcode_recal.realigned-1.bam I=barcode_recal.realigned-2.bam I(x)=barcode_recal.realigned-x.bam O=sample.merged.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedMarkDuplicates">
          <STEP_INDEX>11</STEP_INDEX>
          <PREV_STEP_INDEX>10</PREV_STEP_INDEX>
          <PROGRAM>picard</PROGRAM>
          <VERSION>1.88</VERSION>
          <NOTES>java -jar MarkDuplicates.jar I=sample.merged.bam METRICS_FILE=metric_file.picard O=sample.dups.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedIndexGen">
          <STEP_INDEX>12</STEP_INDEX>
          <PREV_STEP_INDEX>11</PREV_STEP_INDEX>
          <PROGRAM>samtools</PROGRAM>
          <VERSION>0.1.7(r510)</VERSION>
          <NOTES>samtools index sample.dups.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedRealignerTargetCreator">
          <STEP_INDEX>13</STEP_INDEX>
          <PREV_STEP_INDEX>12</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T RealignerTargetCreator -I sample.dups.bam -R reference.fasta -nt 8 --downsampling_type NONE -known 1000G_phase1.indels.b37.vcf.gz -known Mills_and_1000G_gold_standard.indels.b37.vcf.gz -o sample.intervals</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedIndelRealigner">
          <STEP_INDEX>14</STEP_INDEX>
          <PREV_STEP_INDEX>13</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T IndelRealigner -I sample.dups.bam -R reference.fasta -targetIntervals sample.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 sample_realigned.bam</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedBaseRecalibrator">
          <STEP_INDEX>15</STEP_INDEX>
          <PREV_STEP_INDEX>14</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T BaseRecalibrator I=sample_realigned.bam -R reference.fasta -o sample.GATKrecal_data.grp --downsampling_type NONE -knownSites dbsnp_137.b37.vcf.gz -knownSites 1000G_phase1.indels.b37.vcf.gz -knownSites Mills_and_1000G_gold_standard.indels.b37.vcf.gz -cov ReadGroupCovariate -cov QualityScoreCovariate -cov CycleCovariate -cov ContextCovariate-dP illumina -knownSites:dbSNP,VCF sites.vcf.gz -cov ReadGroupCovariate -cov QualityScoreCovariate -cov CycleCovariate -cov DinucCovariate -recalFile sample.csv</NOTES>
        </PIPE_SECTION>
        <PIPE_SECTION section_name="MergedPrintReads">
          <STEP_INDEX>16</STEP_INDEX>
          <PREV_STEP_INDEX>15</PREV_STEP_INDEX>
          <PROGRAM>GATk</PROGRAM>
          <VERSION>2.5-2-gf57256b</VERSION>
          <NOTES>java -jar GenomeAnalysisTK.jar -T PrintReads -I sample_realigned.bam -R reference.fasta -BQSR sample.GATKrecal_data.grp --emit_original_quals --downsampling_type NONE -o sample_recal.realigned.bam</NOTES>
        </PIPE_SECTION>
      </PIPELINE>
    </PROCESSING>
  </RUN>
</RUN_SET>
