..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 2020-10-06, 10:10 based on data in: /beegfs/mk5636/logs/html/HNJW5DRXX/merged


        General Statistics

        Showing 10/10 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HNJW5DRXX_n01_DJ62
        50.4%
        37%
        108.6
        HNJW5DRXX_n01_DJ63
        49.6%
        36%
        122.3
        HNJW5DRXX_n01_DJ64
        44.8%
        36%
        90.5
        HNJW5DRXX_n01_DJ65
        51.6%
        36%
        143.9
        HNJW5DRXX_n01_undetermined
        53.0%
        43%
        95.8
        HNJW5DRXX_n02_DJ62
        46.5%
        37%
        108.6
        HNJW5DRXX_n02_DJ63
        47.7%
        36%
        122.3
        HNJW5DRXX_n02_DJ64
        42.6%
        36%
        90.5
        HNJW5DRXX_n02_DJ65
        48.8%
        36%
        143.9
        HNJW5DRXX_n02_undetermined
        51.3%
        46%
        95.8

        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 9/9 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        95,796,154
        8.8
        DJ62
        108,603,678
        10.6
        DJ63
        122,281,020
        12.0
        DJ64
        90,538,012
        8.9
        DJ65
        143,873,412
        14.1
        DJ66
        135,396,752
        11.6
        DJ67
        132,909,264
        11.4
        DJ68
        151,443,165
        13.0
        DJ69
        112,355,644
        9.6

        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 (%)
        GGGGGGGGTCTTTCCC
        26352203.0
        27.5
        GGGGGGGGGCTTTCCC
        1915444.0
        2.0
        GGGGGGGGGGAAGCAG
        1273331.0
        1.3
        GGGGGGGGAAGACGTC
        1046321.0
        1.1
        GGGGGGGGAAGGATGA
        1035294.0
        1.1
        GGGGGGGGGGAGTACT
        988055.0
        1.0
        CCAAGTCTGCGCCTGT
        912866.0
        0.9
        AACGTTCCGTCTCGCA
        892414.0
        0.9
        GGGGGGGGGCGCCTGT
        841713.0
        0.9
        TTGGACTCATATTCAC
        837724.0
        0.9
        TTGGACTCAAGGATGA
        837225.0
        0.9
        CCAAGTCTGGAAGCAG
        834985.0
        0.9
        GGGGGGGGATATTCAC
        825945.0
        0.9
        GGGGGGGGACTCTATG
        806973.0
        0.8
        ATGTAAGTAAGACGTC
        801448.0
        0.8
        AACGTTCCAAGACGTC
        777343.0
        0.8
        CCAAGTCTATATTCAC
        756896.0
        0.8
        GGGGGGGGGTCTCGCA
        755293.0
        0.8
        TAATACAGGGAAGCAG
        745752.0
        0.8
        GCACGGACAAGACGTC
        733855.0
        0.8

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 4/4 columns.
        Sample NameTotal # of Single-End ReadsTotal # PF Reads% Undetermined% PhiX Aligned
        2.0
        2,553,348,096
        1,093,197,101
        8.8
        2.5

        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 (151bp).


        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..