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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 2020-10-03, 00:10 based on data in: /beegfs/mk5636/logs/html/HNMLVDRXX/merged


        General Statistics

        Showing 20/20 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HNMLVDRXX_n01_dei019
        56.9%
        47%
        34.8
        HNMLVDRXX_n01_dei020
        62.2%
        46%
        48.8
        HNMLVDRXX_n01_dei021
        69.1%
        47%
        37.6
        HNMLVDRXX_n01_dei022
        69.6%
        47%
        44.6
        HNMLVDRXX_n01_dei023
        75.7%
        47%
        36.6
        HNMLVDRXX_n01_dei024
        67.0%
        48%
        44.7
        HNMLVDRXX_n01_dei025
        76.8%
        49%
        30.2
        HNMLVDRXX_n01_dei026
        86.2%
        50%
        42.8
        HNMLVDRXX_n01_dei027
        68.8%
        47%
        40.7
        HNMLVDRXX_n01_dei028
        77.0%
        48%
        40.8
        HNMLVDRXX_n01_dei029
        64.1%
        48%
        37.4
        HNMLVDRXX_n01_dei030
        76.4%
        48%
        34.1
        HNMLVDRXX_n01_dei031
        57.3%
        47%
        42.0
        HNMLVDRXX_n01_dei032
        52.5%
        46%
        45.0
        HNMLVDRXX_n01_dei033
        48.6%
        46%
        37.4
        HNMLVDRXX_n01_dei034
        55.3%
        46%
        37.8
        HNMLVDRXX_n01_dei035
        64.8%
        52%
        42.4
        HNMLVDRXX_n01_dei036
        64.1%
        49%
        42.1
        HNMLVDRXX_n01_dei037
        74.6%
        50%
        41.6
        HNMLVDRXX_n01_undetermined
        91.8%
        45%
        58.4

        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 20/20 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        58,393,294
        7.1
        dei019
        34,808,761
        4.2
        dei020
        48,822,616
        6.0
        dei021
        37,628,147
        4.6
        dei022
        44,606,377
        5.4
        dei023
        36,558,176
        4.5
        dei024
        44,687,405
        5.5
        dei025
        30,178,724
        3.7
        dei026
        42,763,497
        5.2
        dei027
        40,688,610
        5.0
        dei028
        40,773,221
        5.0
        dei029
        37,386,938
        4.6
        dei030
        34,144,492
        4.2
        dei031
        42,041,115
        5.1
        dei032
        44,987,244
        5.5
        dei033
        37,396,244
        4.6
        dei034
        37,765,307
        4.6
        dei035
        42,418,968
        5.2
        dei036
        42,134,700
        5.1
        dei037
        41,604,650
        5.1

        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
        52644936.0
        90.2
        CAGATC
        948542.0
        1.6
        GCCAAT
        356683.0
        0.6
        CTTGTA
        311497.0
        0.5
        AATAAA
        67839.0
        0.1
        CCGATG
        62071.0
        0.1
        NGGGGG
        57923.0
        0.1
        GGGGGC
        57490.0
        0.1
        CCGTAC
        55662.0
        0.1
        GTCCCG
        52622.0
        0.1
        GGGGGT
        44367.0
        0.1
        CAGTTC
        42538.0
        0.1
        ATTAAA
        41549.0
        0.1
        ATAACC
        41318.0
        0.1
        AATCAT
        38488.0
        0.1
        GGTGGG
        37061.0
        0.1
        CAGTCA
        35517.0
        0.1
        NNNNNN
        34035.0
        0.1
        CTGACC
        34028.0
        0.1
        GTTCGG
        32366.0
        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
        2.0
        1,276,674,048
        819,788,486
        7.1
        6.0

        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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