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        MultiQC: Summarize analysis results for multiple tools and samples in a single report
        Philip Ewels, Måns Magnusson, Sverker Lundin and Max Käller
        Bioinformatics (2016)
        doi: 10.1093/bioinformatics/btw354
        PMID: 27312411
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        About MultiQC

        This report was generated using MultiQC, version 1.34

        MultiQC is published in Bioinformatics:

        MultiQC: Summarize analysis results for multiple tools and samples in a single report
        Philip Ewels, Måns Magnusson, Sverker Lundin and Max Käller
        Bioinformatics (2016)
        doi: 10.1093/bioinformatics/btw354
        PMID: 27312411

        MultiQC is developed by Seqera.

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        A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.

        Report generated on 2026-04-30, 14:00 AEST based on data in: /Users/stephen/projects/oncoanalyser_multiqc_plugin/test_data/outputs

        General Statistics

        Showing 4/4 rows and 11/11 columns.
        Sample NameAligmentsReadsMapped ReadsProperly Paired ReadsDuplicate ReadsContaminationPloidyPurityQC PURPLEQC AMBERGender
        case-colo829 hartwig-colo829.normal
        720308024
        702784421
        99.61%
        98.83%
        10.65%
        case-colo829 hartwig-colo829.tumor
        2609124943
        2551026318
        99.60%
        98.76%
        14.62%
        0.00%
        3.1000
        99.00%
        Pass
        Pass
        Male
        case-hcc1395 seqcii-hcc1395.normal
        889908557
        871408807
        99.65%
        98.68%
        2.04%
        case-hcc1395 seqcii-hcc1395.tumor
        1808024698
        1765297342
        99.63%
        98.72%
        3.69%
        0.00%
        2.8200
        100.00%
        Pass
        Pass
        Male

        AMBER

        https://github.com/hartwigmedical/hmftools/tree/master/amber

        Showing 4/4 rows and 5/7 columns.
        Sample NameStatusConsanguinity ProportionContaminationContamination SitesHomozygous Regions PassHomozygous Regions TotalUniparental Disomy
        case-colo829 hartwig-colo829.normal
        0
        252
        case-colo829 hartwig-colo829.tumor
        Pass
        0.00%
        0.00%
        23425
        NONE
        case-hcc1395 seqcii-hcc1395.normal
        3
        253
        case-hcc1395 seqcii-hcc1395.tumor
        Pass
        2.61%
        0.00%
        55643
        NONE

        BamTools

        https://github.com/hartwigmedical/hmftools/tree/master/bam-tools

        Summary

        Showing 4/4 rows and 28/28 columns.
        Sample NameTotal Region BasesTotal ReadsDuplicate ReadsDual Strand ReadsMean CoverageStd Dev CoverageMedian CoverageMAD CoverageLow Map QualDuplicateUnmappedLow Base QualOverlapping ReadCapped CoverageDepth Coverage 1Depth Coverage 5Depth Coverage 10Depth Coverage 15Depth Coverage 20Depth Coverage 25Depth Coverage 30Depth Coverage 40Depth Coverage 50Depth Coverage 60Depth Coverage 70Depth Coverage 80Depth Coverage 90Depth Coverage 100
        case-colo829 hartwig-colo829.normal
        2924985581
        703608192
        74883451
        0
        30.65
        9.64
        32.00
        5.00
        3.36%
        10.50%
        0.28%
        0.01%
        0.49%
        0.00%
        97.78%
        97.17%
        96.43%
        94.09%
        90.11%
        81.68%
        61.41%
        13.08%
        0.98%
        0.18%
        0.10%
        0.07%
        0.05%
        0.03%
        case-colo829 hartwig-colo829.tumor
        2924985581
        2554019777
        373222555
        0
        105.71
        36.86
        108.00
        24.00
        3.25%
        14.40%
        0.29%
        0.01%
        0.73%
        0.16%
        97.36%
        96.93%
        96.72%
        96.57%
        96.45%
        96.33%
        96.20%
        95.92%
        95.43%
        93.21%
        85.95%
        76.37%
        69.35%
        60.96%
        case-hcc1395 seqcii-hcc1395.normal
        2924985581
        873388001
        17745000
        0
        40.93
        14.22
        43.00
        8.00
        3.59%
        1.97%
        0.24%
        0.30%
        1.03%
        0.01%
        97.21%
        96.62%
        96.15%
        95.07%
        92.33%
        87.79%
        82.19%
        61.85%
        26.80%
        5.06%
        0.57%
        0.18%
        0.13%
        0.09%
        case-hcc1395 seqcii-hcc1395.tumor
        2924985581
        1769411736
        65159274
        0
        80.61
        39.60
        75.00
        22.00
        3.94%
        3.56%
        0.26%
        0.28%
        1.53%
        0.10%
        96.75%
        96.17%
        95.91%
        95.66%
        95.25%
        94.47%
        93.13%
        89.21%
        83.00%
        71.19%
        56.42%
        44.54%
        35.28%
        27.18%

        Flag Statistics

        Showing 4/4 rows and 19/19 columns.
        Sample NameAligmentsReadsMapped ReadsDuplicate ReadsProperly Paired ReadsSecondarySupplementaryDuplicatePrimary DuplicateMappedPrimary MappedPairedRead 1Read 2Properly PairedProperly Properly Mate MappedSingletonMate Diff ChrmMate Diff Chrm MAPQ>=5
        case-colo829 hartwig-colo829.normal
        720308024
        702784421
        99.61%
        10.65%
        98.83%
        0
        823771
        74883451
        74857435
        700878318
        700054547
        702784421
        351394086
        351390335
        694537578
        697324673
        2729874
        1954639
        1219564
        case-colo829 hartwig-colo829.tumor
        2609124943
        2551026318
        99.60%
        14.62%
        98.76%
        0
        2993459
        373222555
        373078494
        2543818329
        2540824870
        2551026318
        1275521122
        1275505196
        2519470036
        2530623422
        10201448
        7989738
        5135948
        case-hcc1395 seqcii-hcc1395.normal
        889908557
        871408807
        99.65%
        2.04%
        98.68%
        0
        1979194
        17745000
        17739145
        870377423
        868398229
        871408807
        435691086
        435717721
        859916638
        865387651
        3010578
        2525957
        1510216
        case-hcc1395 seqcii-hcc1395.tumor
        1808024698
        1765297342
        99.63%
        3.69%
        98.72%
        0
        4114394
        65159274
        65137183
        1762895754
        1758781360
        1765297342
        882625967
        882671375
        1742667324
        1752265378
        6515982
        4700156
        2698508

        Coverage

        Created with MultiQC

        Fragment Length

        Created with MultiQC

        PURPLE

        https://github.com/hartwigmedical/hmftools/tree/master/purple

        QC

        Showing 2/2 rows and 12/13 columns.
        Sample NameStatusAMBER GenderCOBALT GenderPurityContaminationTINCLOHAMBER Mean DepthGermline AberrationsMethodDeleted GenesCopy Number SegmentsUnsupported Copy Number Segments
        case-colo829 hartwig-colo829.tumor
        Pass
        Male
        Male
        99.00%
        0.00%
        0.00%
        19.25%
        108
        NONE
        Normal
        4
        238
        0
        case-hcc1395 seqcii-hcc1395.tumor
        Pass
        Male
        Male
        100.00%
        0.00%
        0.00%
        52.43%
        76
        NONE
        Normal
        147
        2741
        4

        Purity Summary

        Showing 2/2 rows and 14/18 columns.
        Sample NameStatusPurityPloidyScoreWhole Genome DuplicationGenderNormalisation factorDiploid ProportionPolyclonal proportionPurity MinimumPurity MaximumPloidy MinimumPloidy MaximumDiploid Proportion MinimumDiploid Proportion MaximumSomatic PenaltyRun ModeTargeted
        case-colo829 hartwig-colo829.tumor
        Normal
        99.00%
        3.1000
        0.6159
        True
        Male
        0.6457
        2.12%
        9.16%
        97.00%
        100.00%
        3.0500
        3.1500
        2.12%
        2.12%
        0.0000
        TUMOR_GERMLINE
        False
        case-hcc1395 seqcii-hcc1395.tumor
        Normal
        100.00%
        2.8200
        1.1965
        True
        Male
        0.7084
        1.74%
        30.82%
        98.00%
        100.00%
        1.3800
        2.9400
        1.67%
        9.85%
        0.0000
        TUMOR_GERMLINE
        False

        Mutational Load

        Showing 2/2 rows and 7/7 columns.
        Sample NameMS StatusTML StatusTMB StatusMS INDELs per MBTMLTMB per MBSV TMB
        case-colo829 hartwig-colo829.tumor
        MSS
        High
        High
        0.0745
        187
        13.7391
        93
        case-hcc1395 seqcii-hcc1395.tumor
        MSS
        High
        High
        0.1035
        350
        14.9171
        1275