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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 2018-07-03, 04:07 based on data in: /beegfs/mk5636/logs/html/HWLKJBGX5/merged


        General Statistics

        Showing 17/17 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc10
        82.0%
        46%
        14.3
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc11
        80.1%
        45%
        9.9
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc12
        81.6%
        45%
        12.2
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc13
        93.3%
        52%
        8.2
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc14
        81.2%
        46%
        12.2
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc15
        91.8%
        52%
        10.0
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc16
        88.8%
        49%
        11.5
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc17
        79.6%
        45%
        12.0
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc18
        80.4%
        45%
        12.2
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc19
        92.8%
        51%
        17.2
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc20
        88.4%
        49%
        17.0
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc21
        96.9%
        50%
        12.9
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc22
        97.2%
        51%
        11.8
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc23
        97.6%
        52%
        14.0
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc24
        97.4%
        52%
        13.0
        HWLKJBGX5_n01_MYCScreens2_5_BC_bc9
        81.3%
        45%
        12.3
        HWLKJBGX5_n01_undetermined
        94.5%
        45%
        72.5

        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 17/17 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        72,528,817
        26.5
        MYCScreens2_5_BC_bc9
        12,283,984
        4.5
        MYCScreens2_5_BC_bc10
        14,325,078
        5.2
        MYCScreens2_5_BC_bc11
        9,876,623
        3.6
        MYCScreens2_5_BC_bc12
        12,184,308
        4.5
        MYCScreens2_5_BC_bc13
        8,241,753
        3.0
        MYCScreens2_5_BC_bc14
        12,240,785
        4.5
        MYCScreens2_5_BC_bc15
        10,005,034
        3.7
        MYCScreens2_5_BC_bc16
        11,545,815
        4.2
        MYCScreens2_5_BC_bc17
        11,976,959
        4.4
        MYCScreens2_5_BC_bc18
        12,201,819
        4.5
        MYCScreens2_5_BC_bc19
        17,244,267
        6.3
        MYCScreens2_5_BC_bc20
        16,963,020
        6.2
        MYCScreens2_5_BC_bc21
        12,905,999
        4.7
        MYCScreens2_5_BC_bc22
        11,847,280
        4.3
        MYCScreens2_5_BC_bc23
        13,998,942
        5.1
        MYCScreens2_5_BC_bc24
        13,017,769
        4.8

        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
        285737208.0
        273,388,252
        26.5
        23.5

        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.

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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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