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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 2020-09-11, 03:09 based on data in: /beegfs/mk5636/logs/html/HFVTNAFX2/merged


        General Statistics

        Showing 22/22 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HFVTNAFX2_n01_AH10517-3H-Hop1mlChIP
        82.7%
        41%
        10.7
        HFVTNAFX2_n01_AH10517-3H-input
        79.4%
        42%
        16.5
        HFVTNAFX2_n01_AH10675-3H-Hop1mlChIP
        66.7%
        43%
        14.4
        HFVTNAFX2_n01_AH10675-3H-input
        71.4%
        47%
        14.6
        HFVTNAFX2_n01_AH10676-3H-Hop1mlChIP
        78.0%
        44%
        15.0
        HFVTNAFX2_n01_AH10676-3H-input
        73.7%
        42%
        10.4
        HFVTNAFX2_n01_AH10677-3H-Hop1mlChIP
        80.8%
        42%
        15.9
        HFVTNAFX2_n01_AH10677-3H-input
        76.0%
        45%
        12.2
        HFVTNAFX2_n01_AH9251-3H-Hop1mlChIP
        75.3%
        41%
        19.4
        HFVTNAFX2_n01_AH9251-3H-input
        82.7%
        39%
        10.2
        HFVTNAFX2_n01_undetermined
        74.2%
        44%
        8.4
        HFVTNAFX2_n02_AH10517-3H-Hop1mlChIP
        76.1%
        46%
        10.7
        HFVTNAFX2_n02_AH10517-3H-input
        74.2%
        43%
        16.5
        HFVTNAFX2_n02_AH10675-3H-Hop1mlChIP
        60.4%
        47%
        14.4
        HFVTNAFX2_n02_AH10675-3H-input
        64.0%
        65%
        14.6
        HFVTNAFX2_n02_AH10676-3H-Hop1mlChIP
        72.3%
        48%
        15.0
        HFVTNAFX2_n02_AH10676-3H-input
        68.3%
        44%
        10.4
        HFVTNAFX2_n02_AH10677-3H-Hop1mlChIP
        75.9%
        44%
        15.9
        HFVTNAFX2_n02_AH10677-3H-input
        70.8%
        47%
        12.2
        HFVTNAFX2_n02_AH9251-3H-Hop1mlChIP
        70.6%
        41%
        19.4
        HFVTNAFX2_n02_AH9251-3H-input
        75.9%
        45%
        10.2
        HFVTNAFX2_n02_undetermined
        71.2%
        52%
        8.4

        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 11/11 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        8,418,939
        5.7
        AH10675-3H-Hop1mlChIP
        14,437,657
        9.8
        AH10675-3H-input
        14,583,163
        9.9
        AH10676-3H-Hop1mlChIP
        15,018,172
        10.2
        AH10676-3H-input
        10,371,884
        7.0
        AH10677-3H-Hop1mlChIP
        15,930,770
        10.8
        AH10677-3H-input
        12,240,153
        8.3
        AH10517-3H-Hop1mlChIP
        10,684,564
        7.2
        AH10517-3H-input
        16,495,480
        11.2
        AH9251-3H-Hop1mlChIP
        19,397,356
        13.1
        AH9251-3H-input
        10,240,778
        6.9

        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
        5540558.0
        65.8
        NNNNNN
        65698.0
        0.8
        ATTTAA
        48570.0
        0.6
        AGAACA
        44452.0
        0.5
        CCCGTC
        41398.0
        0.5
        AGATCA
        40664.0
        0.5
        AAATAA
        32507.0
        0.4
        AAGAAA
        30720.0
        0.4
        CAGTCA
        30448.0
        0.4
        ACATAC
        30018.0
        0.4
        GGGGGC
        29377.0
        0.3
        ACACAA
        28945.0
        0.3
        GGGGGT
        28940.0
        0.3
        ATAACA
        28658.0
        0.3
        GCGGGG
        25898.0
        0.3
        GGGGCC
        25809.0
        0.3
        CGGGGG
        25401.0
        0.3
        ATTAAA
        24877.0
        0.3
        CCCAAA
        24170.0
        0.3
        CGATCA
        23604.0
        0.3

        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
        167,099,904
        147,818,916
        5.7
        2.7

        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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