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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 2019-05-29, 23:05 based on data in: /beegfs/mk5636/logs/html/HGKGNBGXB/merged


        General Statistics

        Showing 16/16 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HGKGNBGXB_n01_dpr1
        36.7%
        49%
        11.9
        HGKGNBGXB_n01_dpr2
        64.9%
        48%
        7.7
        HGKGNBGXB_n01_dpr3
        61.3%
        48%
        3.3
        HGKGNBGXB_n01_mb218
        17.5%
        45%
        34.1
        HGKGNBGXB_n01_mb219
        5.3%
        46%
        35.0
        HGKGNBGXB_n01_mb220
        15.4%
        45%
        30.8
        HGKGNBGXB_n01_mb221
        5.7%
        46%
        34.1
        HGKGNBGXB_n01_mb222
        21.4%
        45%
        25.9
        HGKGNBGXB_n01_mb223
        5.6%
        46%
        33.7
        HGKGNBGXB_n01_mb224
        28.3%
        42%
        25.9
        HGKGNBGXB_n01_mb225
        26.5%
        42%
        22.4
        HGKGNBGXB_n01_mb226
        29.9%
        43%
        31.4
        HGKGNBGXB_n01_mb227
        29.8%
        43%
        30.2
        HGKGNBGXB_n01_mb228
        55.2%
        43%
        28.2
        HGKGNBGXB_n01_mb229
        27.3%
        41%
        22.1
        HGKGNBGXB_n01_undetermined
        58.3%
        55%
        38.9

        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 16/16 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        38,932,568
        9.4
        mb218
        34,145,523
        8.2
        mb219
        35,008,765
        8.4
        mb220
        30,785,353
        7.4
        mb221
        34,068,754
        8.2
        mb222
        25,888,781
        6.2
        mb223
        33,738,820
        8.1
        mb224
        25,868,735
        6.2
        mb225
        22,397,996
        5.4
        mb226
        31,444,041
        7.6
        mb227
        30,181,213
        7.3
        mb228
        28,223,578
        6.8
        mb229
        22,097,064
        5.3
        dpr1
        11,865,498
        2.9
        dpr2
        7,702,142
        1.9
        dpr3
        3,324,398
        0.8

        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
        28229437.0
        72.5
        GGGGGT
        185408.0
        0.5
        GCTACA
        176563.0
        0.5
        GGGGGC
        160365.0
        0.4
        ATCAGA
        158431.0
        0.4
        GGGGTG
        139834.0
        0.4
        GATGTA
        135654.0
        0.3
        TTAGCA
        130623.0
        0.3
        CGGGGG
        115657.0
        0.3
        GGCGGG
        113392.0
        0.3
        ACTGAA
        112647.0
        0.3
        ACAGGA
        112445.0
        0.3
        GGTGGG
        109404.0
        0.3
        GGTACA
        108512.0
        0.3
        TGCCAA
        107083.0
        0.3
        TACCAA
        102851.0
        0.3
        GCCATA
        102589.0
        0.3
        GGGGCG
        100104.0
        0.3
        GCAATA
        98616.0
        0.2
        GGCTCA
        97899.0
        0.2

        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
        495,665,704
        415,673,229
        9.4
        3.2

        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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