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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 2020-03-06, 15:03 based on data in: /beegfs/mk5636/logs/html/HCCYVBGXF/merged


        General Statistics

        Showing 26/26 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HCCYVBGXF_n01_A.F1.fcWGA
        40.8%
        46%
        34.8
        HCCYVBGXF_n01_A.F1.fdWGA
        29.5%
        45%
        31.8
        HCCYVBGXF_n01_A.F1.fgWGA
        21.0%
        45%
        32.4
        HCCYVBGXF_n01_A.F1.fhWGA
        26.9%
        45%
        31.8
        HCCYVBGXF_n01_A.F1.meWGA
        31.1%
        45%
        38.7
        HCCYVBGXF_n01_A.F1.mfWGA
        37.8%
        45%
        36.0
        HCCYVBGXF_n01_B.F1.faWGA
        33.6%
        47%
        30.2
        HCCYVBGXF_n01_B.F1.fcWGA
        37.7%
        44%
        41.5
        HCCYVBGXF_n01_B.F1.fdWGA
        30.2%
        45%
        43.9
        HCCYVBGXF_n01_B.F1.ffWGA
        44.1%
        46%
        39.8
        HCCYVBGXF_n01_B.F1.mbWGA
        32.2%
        45%
        31.9
        HCCYVBGXF_n01_B.F1.mhWGA
        23.9%
        45%
        32.3
        HCCYVBGXF_n01_undetermined
        71.4%
        51%
        16.5
        HCCYVBGXF_n02_A.F1.fcWGA
        38.8%
        47%
        34.8
        HCCYVBGXF_n02_A.F1.fdWGA
        27.2%
        45%
        31.8
        HCCYVBGXF_n02_A.F1.fgWGA
        19.6%
        45%
        32.4
        HCCYVBGXF_n02_A.F1.fhWGA
        25.1%
        45%
        31.8
        HCCYVBGXF_n02_A.F1.meWGA
        29.3%
        45%
        38.7
        HCCYVBGXF_n02_A.F1.mfWGA
        35.9%
        45%
        36.0
        HCCYVBGXF_n02_B.F1.faWGA
        31.0%
        47%
        30.2
        HCCYVBGXF_n02_B.F1.fcWGA
        35.8%
        44%
        41.5
        HCCYVBGXF_n02_B.F1.fdWGA
        28.6%
        45%
        43.9
        HCCYVBGXF_n02_B.F1.ffWGA
        42.1%
        46%
        39.8
        HCCYVBGXF_n02_B.F1.mbWGA
        30.2%
        45%
        31.9
        HCCYVBGXF_n02_B.F1.mhWGA
        22.4%
        45%
        32.3
        HCCYVBGXF_n02_undetermined
        69.8%
        51%
        16.5

        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 13/13 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        16,474,334
        3.7
        A.F1.fcWGA
        34,769,333
        7.9
        A.F1.fdWGA
        31,798,385
        7.2
        A.F1.meWGA
        38,736,984
        8.8
        A.F1.mfWGA
        35,978,830
        8.1
        A.F1.fgWGA
        32,444,478
        7.3
        A.F1.fhWGA
        31,846,640
        7.2
        B.F1.faWGA
        30,189,150
        6.8
        B.F1.mbWGA
        31,884,932
        7.2
        B.F1.fcWGA
        41,484,493
        9.4
        B.F1.fdWGA
        43,900,450
        9.9
        B.F1.ffWGA
        39,836,685
        9.0
        B.F1.mhWGA
        32,272,138
        7.3

        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
        13670706.0
        83.0
        GTTCGG
        67853.0
        0.4
        GTGGGG
        57609.0
        0.3
        NNNNNN
        49085.0
        0.3
        ATCCTT
        45514.0
        0.3
        GGGGCG
        39982.0
        0.2
        GGGGGC
        37257.0
        0.2
        GGTGGG
        35830.0
        0.2
        ATTACA
        33119.0
        0.2
        ATTAAA
        30791.0
        0.2
        GGGGGT
        30069.0
        0.2
        AGTCCG
        29106.0
        0.2
        GCGGGG
        28891.0
        0.2
        GTACGT
        28398.0
        0.2
        GTCGCA
        26348.0
        0.2
        CGACGT
        24379.0
        0.1
        GTTTTC
        23175.0
        0.1
        CCCGTC
        22099.0
        0.1
        CCGCCG
        21891.0
        0.1
        GAGGGA
        21086.0
        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
        495,400,168
        441,616,832
        3.7
        2.3

        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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