..plots loading..

Highlight Samples

Regex mode off

    Rename Samples

    Click here for bulk input.

    Paste two columns of a tab-delimited table here (eg. from Excel).

    First column should be the old name, second column the new name.

    Regex mode off

      Show / Hide Samples

      Regex mode off

        Export Plots

        px
        px
        X

        Download the raw data used to create the plots in this report below:

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


        Choose Plots

        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

        Save Settings

        You can save the toolbox settings for this report to the browser.


        Load Settings

        Choose a saved report profile from the dropdown box below:

        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 2019-04-16, 23:04 based on data in: /beegfs/mk5636/logs/html/H7K37BGXB/merged


        General Statistics

        Showing 13/13 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        H7K37BGXB_n01_1_NLP7_ab_R1
        74.1%
        45%
        17.4
        H7K37BGXB_n01_1_NLP7_novus_R1
        72.7%
        44%
        23.4
        H7K37BGXB_n01_2_NLP7_ab_R2
        82.3%
        46%
        16.0
        H7K37BGXB_n01_2_NLP7_novus_R2
        86.0%
        47%
        21.1
        H7K37BGXB_n01_3_NLP7_ab_R3
        73.8%
        46%
        12.0
        H7K37BGXB_n01_3_NLP7_novus_R3
        78.8%
        45%
        17.9
        H7K37BGXB_n01_4_NLP7_ab_R4
        82.0%
        45%
        22.0
        H7K37BGXB_n01_4_NLP7_novus_R4
        69.3%
        45%
        13.8
        H7K37BGXB_n01_5_NLP7_ab_R5
        79.8%
        46%
        24.6
        H7K37BGXB_n01_5_NLP7_novus_R5
        78.9%
        45%
        13.1
        H7K37BGXB_n01_input_NLP7_R1
        74.6%
        42%
        48.6
        H7K37BGXB_n01_input_NLP7_R2
        87.0%
        43%
        26.6
        H7K37BGXB_n01_undetermined
        91.5%
        60%
        36.5

        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
        36,454,027
        12.4
        1_NLP7_novus_R1
        23,399,785
        8.0
        2_NLP7_novus_R2
        21,077,328
        7.2
        3_NLP7_novus_R3
        17,917,452
        6.1
        4_NLP7_novus_R4
        13,822,845
        4.7
        5_NLP7_novus_R5
        13,095,288
        4.5
        1_NLP7_ab_R1
        17,371,424
        5.9
        2_NLP7_ab_R2
        15,982,062
        5.5
        3_NLP7_ab_R3
        12,038,678
        4.1
        4_NLP7_ab_R4
        22,000,796
        7.5
        5_NLP7_ab_R5
        24,592,060
        8.4
        input_NLP7_R1
        48,632,797
        16.6
        input_NLP7_R2
        26,585,257
        9.1

        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
        32769449.0
        89.9
        GTGGGG
        317132.0
        0.9
        GGTGGG
        145114.0
        0.4
        GGGGCG
        135025.0
        0.4
        GGGTGG
        115762.0
        0.3
        GGGGGC
        95622.0
        0.3
        GTTCGG
        95359.0
        0.3
        CGGGGG
        85949.0
        0.2
        GGGGTG
        58512.0
        0.2
        NNNNNN
        55919.0
        0.1
        AGGGGG
        55863.0
        0.1
        GGCGGG
        50378.0
        0.1
        GTTGGG
        46964.0
        0.1
        TGGGGG
        38140.0
        0.1
        GGGCGG
        34385.0
        0.1
        GGGTCG
        34346.0
        0.1
        GGTTGG
        32618.0
        0.1
        GTTTTC
        32470.0
        0.1
        NGGGGG
        27937.0
        0.1
        GCGGGG
        27614.0
        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
        320,566,208
        292,969,799
        12.4
        7.8

        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.

        loading..

        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.

        loading..

        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.

        loading..

        Per Base N Content

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

        loading..

        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.

        loading..

        Overrepresented sequences

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

        loading..

        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.

        loading..