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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 2020-06-09, 21:06 based on data in: /beegfs/mk5636/logs/html/HNLNGBGXF/merged


        General Statistics

        Showing 38/38 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HNLNGBGXF_n01_DG4446_AP1_mRNA
        39.9%
        48%
        31.2
        HNLNGBGXF_n01_DG4450_AM1_mRNA
        39.2%
        49%
        31.4
        HNLNGBGXF_n01_DG4460_ADI1_mRNA
        41.2%
        48%
        33.0
        HNLNGBGXF_n01_DG4474_ADI2_mRNA
        40.2%
        49%
        33.5
        HNLNGBGXF_n01_DG4476_AM2_mRNA
        38.1%
        49%
        30.6
        HNLNGBGXF_n01_DG4478_AP2_mRNA
        38.9%
        48%
        31.8
        HNLNGBGXF_n01_DG4565_AP3_mRNA
        35.8%
        48%
        23.9
        HNLNGBGXF_n01_DG4567_ADI3_mRNA
        41.5%
        48%
        31.5
        HNLNGBGXF_n01_DG4579_AM3_mRNA
        39.5%
        48%
        30.9
        HNLNGBGXF_n01_DG4593_AP4_mRNA
        37.9%
        48%
        31.5
        HNLNGBGXF_n01_DG4595_ADI4_mRNA
        39.9%
        48%
        30.7
        HNLNGBGXF_n01_DG4597_AP5_mRNA
        38.9%
        48%
        32.2
        HNLNGBGXF_n01_DG4599_ADI5_mRNA
        39.8%
        48%
        30.0
        HNLNGBGXF_n01_DG4601_AM4_mRNA
        38.8%
        48%
        29.3
        HNLNGBGXF_n01_FDK236_LP1_mRNA
        38.1%
        48%
        26.6
        HNLNGBGXF_n01_FDK241_LM2_mRNA
        41.3%
        48%
        29.9
        HNLNGBGXF_n01_FDK262_LM1_mRNA
        38.7%
        48%
        30.5
        HNLNGBGXF_n01_FDK287_LM3_mRNA
        35.6%
        48%
        19.3
        HNLNGBGXF_n01_undetermined
        31.2%
        51%
        20.9
        HNLNGBGXF_n02_DG4446_AP1_mRNA
        36.1%
        48%
        31.2
        HNLNGBGXF_n02_DG4450_AM1_mRNA
        37.0%
        48%
        31.4
        HNLNGBGXF_n02_DG4460_ADI1_mRNA
        37.8%
        48%
        33.0
        HNLNGBGXF_n02_DG4474_ADI2_mRNA
        37.9%
        49%
        33.5
        HNLNGBGXF_n02_DG4476_AM2_mRNA
        35.2%
        49%
        30.6
        HNLNGBGXF_n02_DG4478_AP2_mRNA
        31.3%
        49%
        31.8
        HNLNGBGXF_n02_DG4565_AP3_mRNA
        31.1%
        49%
        23.9
        HNLNGBGXF_n02_DG4567_ADI3_mRNA
        39.7%
        48%
        31.5
        HNLNGBGXF_n02_DG4579_AM3_mRNA
        37.4%
        48%
        30.9
        HNLNGBGXF_n02_DG4593_AP4_mRNA
        36.0%
        48%
        31.5
        HNLNGBGXF_n02_DG4595_ADI4_mRNA
        37.4%
        48%
        30.7
        HNLNGBGXF_n02_DG4597_AP5_mRNA
        36.5%
        48%
        32.2
        HNLNGBGXF_n02_DG4599_ADI5_mRNA
        37.0%
        48%
        30.0
        HNLNGBGXF_n02_DG4601_AM4_mRNA
        37.1%
        48%
        29.3
        HNLNGBGXF_n02_FDK236_LP1_mRNA
        33.4%
        49%
        26.6
        HNLNGBGXF_n02_FDK241_LM2_mRNA
        39.0%
        48%
        29.9
        HNLNGBGXF_n02_FDK262_LM1_mRNA
        36.3%
        48%
        30.5
        HNLNGBGXF_n02_FDK287_LM3_mRNA
        33.2%
        48%
        19.3
        HNLNGBGXF_n02_undetermined
        25.2%
        50%
        20.9

        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 19/19 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        20,865,456
        3.7
        DG4450_AM1_mRNA
        31,414,823
        5.6
        DG4476_AM2_mRNA
        30,633,130
        5.5
        DG4579_AM3_mRNA
        30,943,231
        5.5
        DG4601_AM4_mRNA
        29,347,992
        5.3
        DG4446_AP1_mRNA
        31,209,170
        5.6
        DG4478_AP2_mRNA
        31,815,002
        5.7
        DG4565_AP3_mRNA
        23,917,514
        4.3
        DG4593_AP4_mRNA
        31,535,853
        5.6
        DG4597_AP5_mRNA
        32,200,939
        5.8
        DG4460_ADI1_mRNA
        33,002,074
        5.9
        DG4474_ADI2_mRNA
        33,493,426
        6.0
        DG4567_ADI3_mRNA
        31,469,512
        5.6
        DG4595_ADI4_mRNA
        30,687,359
        5.5
        DG4599_ADI5_mRNA
        29,998,330
        5.4
        FDK262_LM1_mRNA
        30,460,277
        5.5
        FDK241_LM2_mRNA
        29,944,266
        5.4
        FDK287_LM3_mRNA
        19,269,562
        3.4
        FDK236_LP1_mRNA
        26,613,498
        4.8

        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 (%)
        GGGGGGGGAGATCTCG
        1450320.0
        7.0
        GGGGGGGGGGGGGGGG
        1169548.0
        5.6
        GGGGGGGGGCCTCTAT
        589217.0
        2.8
        GGGGGGGGAGGCTATA
        585068.0
        2.8
        GGGGGGGGAGGATAGG
        543950.0
        2.6
        GGGGGGGGTCAGAGCC
        499629.0
        2.4
        TCCGGAGAGGGGGGGG
        221839.0
        1.1
        ATTACTCGGGGGGGGG
        218352.0
        1.1
        CGCTCATTGGGGGGGG
        205332.0
        1.0
        GAGATTCCGGGGGGGG
        204419.0
        1.0
        ATTCAGAAGGGGGGGG
        72683.0
        0.3
        TCCGGAGAGCCTCGAG
        64402.0
        0.3
        TCCGGAGAGCCGCGAT
        59400.0
        0.3
        TCGGAGAAAGGATAGG
        43431.0
        0.2
        ATTACTCGAGGATATT
        42869.0
        0.2
        GCTCATTAAGGATAGG
        42499.0
        0.2
        TCGGAGAAGCCTCTAT
        40870.0
        0.2
        CGCTCATTAGGATATT
        40776.0
        0.2
        TCGGAGAAAGGCTATA
        40590.0
        0.2
        GCTCATTAAGGCTATA
        39840.0
        0.2

        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
        679,478,464
        558,821,414
        3.7
        0.3

        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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