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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 2019-03-09, 04:03 based on data in: /beegfs/mk5636/logs/html/HYKTJBGX9/merged


        General Statistics

        Showing 17/17 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HYKTJBGX9_n01_PT1
        67.0%
        43%
        19.4
        HYKTJBGX9_n01_PT10
        50.6%
        43%
        28.3
        HYKTJBGX9_n01_PT11
        53.7%
        43%
        33.4
        HYKTJBGX9_n01_PT12
        50.4%
        44%
        26.9
        HYKTJBGX9_n01_PT16
        65.1%
        46%
        31.5
        HYKTJBGX9_n01_PT17
        53.1%
        43%
        28.5
        HYKTJBGX9_n01_PT2
        64.1%
        48%
        28.4
        HYKTJBGX9_n01_PT3
        50.2%
        47%
        14.4
        HYKTJBGX9_n01_PT4
        63.2%
        48%
        25.6
        HYKTJBGX9_n01_PT5
        67.0%
        48%
        31.8
        HYKTJBGX9_n01_PT6
        59.6%
        48%
        27.0
        HYKTJBGX9_n01_PT7
        52.1%
        41%
        25.5
        HYKTJBGX9_n01_PT8
        82.4%
        43%
        22.5
        HYKTJBGX9_n01_PT9
        41.8%
        43%
        19.8
        HYKTJBGX9_n01_WV1
        60.5%
        45%
        34.3
        HYKTJBGX9_n01_WV2
        57.6%
        44%
        22.4
        HYKTJBGX9_n01_undetermined
        82.7%
        48%
        35.8

        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 17/17 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        35,833,205
        7.9
        PT1
        19,361,987
        4.3
        PT2
        28,384,352
        6.2
        PT3
        14,400,642
        3.2
        PT4
        25,629,566
        5.6
        PT5
        31,794,021
        7.0
        PT6
        26,989,292
        5.9
        PT7
        25,467,187
        5.6
        PT8
        22,457,472
        4.9
        PT9
        19,785,679
        4.3
        PT10
        28,259,275
        6.2
        PT11
        33,371,229
        7.3
        PT12
        26,928,627
        5.9
        PT16
        31,516,535
        6.9
        PT17
        28,530,097
        6.3
        WV1
        34,342,598
        7.5
        WV2
        22,407,341
        4.9

        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
        30372279.0
        84.8
        NNNNNN
        347989.0
        1.0
        GTGGGG
        138831.0
        0.4
        GGGGGC
        127135.0
        0.3
        GGGGCG
        95289.0
        0.3
        GGGGTG
        95272.0
        0.3
        GGGTGG
        79255.0
        0.2
        GGTGGG
        74529.0
        0.2
        GGGGGT
        70129.0
        0.2
        GGGCGG
        64614.0
        0.2
        GCGGGG
        61708.0
        0.2
        GNNNNN
        60921.0
        0.2
        TGGGGG
        44288.0
        0.1
        GGCGGG
        42516.0
        0.1
        GTTCGG
        39447.0
        0.1
        ANNNNN
        32472.0
        0.1
        GACAAA
        31410.0
        0.1
        CGTCCG
        30434.0
        0.1
        CGGGGG
        30426.0
        0.1
        AGGGGG
        26349.0
        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
        530,185,136
        455,459,105
        7.9
        5.8

        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 (101bp).


        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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