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        Note that additional data was saved in multiqc_data when this report was generated.


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        If you use plots from MultiQC in a publication or presentation, please cite:

        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 1.0.dev0

        You can see a YouTube video describing how to use MultiQC reports here: https://youtu.be/qPbIlO_KWN0

        For more information about MultiQC, including other videos and extensive documentation, please visit http://multiqc.info

        You can report bugs, suggest improvements and find the source code for MultiQC on GitHub: https://github.com/ewels/MultiQC

        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

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

        Report generated on 2020-03-03, 03:03 based on data in: /beegfs/mk5636/logs/html/HCV3NBGXF/merged


        General Statistics

        Showing 22/22 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HCV3NBGXF_n01_AM66
        66.5%
        47%
        13.4
        HCV3NBGXF_n01_AM67
        66.7%
        46%
        14.8
        HCV3NBGXF_n01_AM68
        65.9%
        47%
        12.3
        HCV3NBGXF_n01_AM69
        64.5%
        46%
        11.4
        HCV3NBGXF_n01_AM70
        63.3%
        46%
        8.4
        HCV3NBGXF_n01_AM71
        70.3%
        46%
        13.6
        HCV3NBGXF_n01_AM72
        67.4%
        46%
        12.1
        HCV3NBGXF_n01_AM73
        64.7%
        46%
        10.8
        HCV3NBGXF_n01_AM74
        68.3%
        46%
        16.0
        HCV3NBGXF_n01_AM75
        66.3%
        47%
        14.7
        HCV3NBGXF_n01_AM76
        61.7%
        46%
        12.9
        HCV3NBGXF_n01_AM77
        66.3%
        46%
        14.4
        HCV3NBGXF_n01_AM82
        76.2%
        48%
        20.9
        HCV3NBGXF_n01_AM83
        77.0%
        48%
        20.9
        HCV3NBGXF_n01_AM84
        76.6%
        48%
        21.1
        HCV3NBGXF_n01_AM85
        72.6%
        48%
        20.2
        HCV3NBGXF_n01_AM86
        73.7%
        48%
        18.4
        HCV3NBGXF_n01_AM87
        71.9%
        48%
        16.7
        HCV3NBGXF_n01_AM88
        32.1%
        41%
        15.4
        HCV3NBGXF_n01_AM89
        30.6%
        47%
        16.5
        HCV3NBGXF_n01_AM90
        20.7%
        45%
        19.9
        HCV3NBGXF_n01_undetermined
        85.4%
        53%
        35.7

        Demultiplexing Report

        Demultiplexing Report
        Total Read Count: Total number of PF (Passing Filter) reads in this library.
        Portion: The proportion of reads that represent the individual library in the entire Library Pool.

        Showing 22/22 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        35,670,792
        9.9
        AM66
        13,440,813
        3.7
        AM67
        14,847,770
        4.1
        AM68
        12,262,155
        3.4
        AM69
        11,391,648
        3.2
        AM70
        8,413,104
        2.3
        AM71
        13,626,344
        3.8
        AM72
        12,104,353
        3.4
        AM73
        10,826,034
        3.0
        AM74
        16,010,804
        4.4
        AM75
        14,690,709
        4.1
        AM76
        12,941,891
        3.6
        AM77
        14,419,269
        4.0
        AM82
        20,904,213
        5.8
        AM83
        20,931,399
        5.8
        AM84
        21,116,968
        5.9
        AM85
        20,227,010
        5.6
        AM86
        18,411,312
        5.1
        AM87
        16,654,944
        4.6
        AM88
        15,442,564
        4.3
        AM89
        16,519,686
        4.6
        AM90
        19,884,013
        5.5

        Barcodes of Undetermined Reads

        Barcodes of Undetermined Reads
        We have determined the barcodes of your undetermined reads (reads containing a barcode that you did not encode in your metadata). Here are the top 20 barcodes belonging to the undetermined reads. The full list is available here.

        Showing 20/20 rows and 2/2 columns.
        Sample NameCountFrequency (%)
        GGGGGG
        30891825.0
        86.6
        GGGGGC
        96454.0
        0.3
        GGGGGT
        77603.0
        0.2
        GTGGGG
        76842.0
        0.2
        GGGGCG
        70913.0
        0.2
        GGGTGG
        69138.0
        0.2
        GGTGGG
        63054.0
        0.2
        CCCGTC
        58110.0
        0.2
        GGGGTG
        55456.0
        0.2
        NNNNNN
        49007.0
        0.1
        GGGCGG
        46165.0
        0.1
        GTCCCG
        39588.0
        0.1
        CAGTCA
        38046.0
        0.1
        TGGGGG
        31142.0
        0.1
        GGCGGG
        30380.0
        0.1
        CCGATG
        28079.0
        0.1
        GCGGGG
        27901.0
        0.1
        CGGGGG
        27589.0
        0.1
        GGGCCC
        26743.0
        0.1
        GGGGGA
        24870.0
        0.1

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 4/4 columns.
        Sample NameTotal # of Single-End ReadsTotal # PF Reads% Undetermined% PhiX Aligned
        4.0
        399,373,416
        360,737,795
        9.9
        4.8

        FastQC

        FastQC is a quality control tool for high throughput sequence data, written by Simon Andrews at the Babraham Institute in Cambridge.

        Sequence Quality Histograms

        The mean quality value across each base position in the read. See the FastQC help.

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        Per Sequence Quality Scores

        The number of reads with average quality scores. Shows if a subset of reads has poor quality. See the FastQC help.

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        Per Base Sequence Content

        The proportion of each base position for which each of the four normal DNA bases has been called. See the FastQC help.

        Click a heatmap row to see a line plot for that dataset.

        rollover for sample name
        Position: -
        %T: -
        %C: -
        %A: -
        %G: -

        Per Sequence GC Content

        The average GC content of reads. Normal random library typically have a roughly normal distribution of GC content. See the FastQC help.

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        Per Base N Content

        The percentage of base calls at each position for which an N was called. See the FastQC help.

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        Sequence Length Distribution

        All samples have sequences of a single length (76bp).


        Sequence Duplication Levels

        The relative level of duplication found for every sequence. See the FastQC help.

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        Overrepresented sequences

        The total amount of overrepresented sequences found in each library. See the FastQC help for further information.

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        Adapter Content

        The cumulative percentage count of the proportion of your library which has seen each of the adapter sequences at each position. See the FastQC help. Only samples with ≥ 0.1% adapter contamination are shown.

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