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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 2019-02-27, 05:02 based on data in: /beegfs/mk5636/logs/html/HWCLJBGX9/merged


        General Statistics

        Showing 18/18 rows and 4/5 columns.
        Sample Name% Dups% GCLengthM Seqs
        HWCLJBGX9_n01_190222-lib1a
        28.7%
        48%
        26
        27.8
        HWCLJBGX9_n01_190222-lib1b
        39.0%
        48%
        26
        44.8
        HWCLJBGX9_n01_190222-lib1c
        28.6%
        48%
        26
        27.6
        HWCLJBGX9_n01_190222-lib1d
        29.8%
        48%
        26
        28.7
        HWCLJBGX9_n01_190222-lib2a
        50.7%
        48%
        26
        53.6
        HWCLJBGX9_n01_190222-lib2b
        53.1%
        48%
        26
        58.3
        HWCLJBGX9_n01_190222-lib2c
        51.6%
        48%
        26
        55.7
        HWCLJBGX9_n01_190222-lib2d
        53.2%
        48%
        26
        59.2
        HWCLJBGX9_n01_undetermined
        77.2%
        51%
        26
        27.8
        HWCLJBGX9_n02_190222-lib1a
        68.1%
        41%
        49
        27.8
        HWCLJBGX9_n02_190222-lib1b
        68.4%
        42%
        49
        44.8
        HWCLJBGX9_n02_190222-lib1c
        68.0%
        41%
        49
        27.6
        HWCLJBGX9_n02_190222-lib1d
        67.2%
        41%
        49
        28.7
        HWCLJBGX9_n02_190222-lib2a
        69.3%
        40%
        49
        53.6
        HWCLJBGX9_n02_190222-lib2b
        68.7%
        40%
        49
        58.3
        HWCLJBGX9_n02_190222-lib2c
        68.8%
        40%
        49
        55.7
        HWCLJBGX9_n02_190222-lib2d
        67.8%
        40%
        49
        59.2
        HWCLJBGX9_n02_undetermined
        79.9%
        51%
        49
        27.8

        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 9/9 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        27,824,405
        7.3
        190222-lib1a
        27,842,550
        7.3
        190222-lib1b
        44,798,115
        11.7
        190222-lib1c
        27,551,145
        7.2
        190222-lib1d
        28,671,133
        7.5
        190222-lib2a
        53,648,304
        14.0
        190222-lib2b
        58,340,353
        15.2
        190222-lib2c
        55,651,406
        14.5
        190222-lib2d
        59,217,683
        15.4

        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
        22810972.0
        82.0
        TGCAAGCA
        113545.0
        0.4
        AAGTGCTA
        87828.0
        0.3
        CTGCAGCA
        67930.0
        0.2
        GCTACTGA
        66102.0
        0.2
        CGCAAGCA
        62218.0
        0.2
        GGGGGGTG
        60378.0
        0.2
        GGGGGGGT
        58186.0
        0.2
        CTCAAGCA
        50411.0
        0.2
        GGGGGGCG
        45977.0
        0.2
        GGGGGCGG
        45134.0
        0.2
        AAGGTGAA
        44584.0
        0.2
        CTACCTGA
        44134.0
        0.2
        GGGGGGTA
        42732.0
        0.1
        GCTACCGA
        42719.0
        0.1
        CTGAAGCA
        41405.0
        0.1
        GCACCTGA
        40050.0
        0.1
        GCGGGGGG
        40007.0
        0.1
        TGGGGGGG
        39953.0
        0.1
        TGCTTAAA
        39536.0
        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
        420,272,944
        383,545,094
        7.3
        4.6

        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 (49bp , 26bp). 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%