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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 2019-06-11, 01:06 based on data in: /beegfs/mk5636/logs/html/HKYKWAFXY/merged


        General Statistics

        Showing 10/10 rows and 4/5 columns.
        Sample Name% Dups% GCLengthM Seqs
        HKYKWAFXY_n01_CCPD50
        89.8%
        44%
        71
        36.2
        HKYKWAFXY_n01_CCPD51
        89.5%
        48%
        71
        30.6
        HKYKWAFXY_n01_CCPD52
        89.4%
        46%
        71
        30.3
        HKYKWAFXY_n01_CCPD53
        87.6%
        48%
        71
        15.7
        HKYKWAFXY_n01_undetermined
        85.4%
        67%
        71
        10.7
        HKYKWAFXY_n02_CCPD50
        98.6%
        40%
        41
        36.2
        HKYKWAFXY_n02_CCPD51
        98.2%
        39%
        41
        30.6
        HKYKWAFXY_n02_CCPD52
        97.7%
        40%
        41
        30.3
        HKYKWAFXY_n02_CCPD53
        97.5%
        43%
        41
        15.7
        HKYKWAFXY_n02_undetermined
        81.0%
        67%
        41
        10.7

        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 5/5 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        10,665,607
        8.6
        CCPD50
        36,154,925
        29.3
        CCPD51
        30,582,078
        24.8
        CCPD52
        30,269,947
        24.5
        CCPD53
        15,705,805
        12.7

        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 (%)
        GGGGGGGG
        9086715.0
        85.2
        ACGCGCGA
        68603.0
        0.6
        GACGTGTA
        34297.0
        0.3
        CGACATGA
        30996.0
        0.3
        NNNNNNNN
        29106.0
        0.3
        GCTCTACT
        29009.0
        0.3
        CAACCTGT
        27023.0
        0.2
        GATCTACT
        23161.0
        0.2
        TCTACTTA
        20491.0
        0.2
        CAAAAATT
        19956.0
        0.2
        CGCTCCAG
        19663.0
        0.2
        AAACCTCT
        18022.0
        0.2
        ACCGGCGA
        17747.0
        0.2
        ACCCGCGA
        17517.0
        0.2
        AACTACAT
        17201.0
        0.2
        GCGGGGGG
        16815.0
        0.2
        CGGGGGGG
        15674.0
        0.1
        ACCGCCGA
        15470.0
        0.1
        ACCTCCAG
        15193.0
        0.1
        GGGGGGGT
        12978.0
        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
        142,574,164
        123,378,362
        8.6
        3.2

        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 (41bp , 71bp). See the General Statistics Table.


        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.

        No samples found with any adapter contamination > 0.1%