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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 2020-03-12, 18:03 based on data in: /beegfs/mk5636/logs/html/H3V73AFX2/merged


        General Statistics

        Showing 19/19 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        H3V73AFX2_n01_CD4_CFSE_high
        91.6%
        49%
        0.0
        H3V73AFX2_n01_CD4_CFSE_high_corrected
        99.4%
        49%
        9.9
        H3V73AFX2_n01_CD4_CFSE_low
        51.3%
        50%
        0.0
        H3V73AFX2_n01_CD4_CFSE_low_corrected
        99.4%
        49%
        11.9
        H3V73AFX2_n01_CD4_presort
        76.5%
        49%
        0.0
        H3V73AFX2_n01_CD4_presort_corrected
        99.4%
        49%
        11.5
        H3V73AFX2_n01_CD4_prestim
        90.8%
        49%
        0.0
        H3V73AFX2_n01_CD4_prestim_corrected
        99.5%
        49%
        11.6
        H3V73AFX2_n01_CD8_CFSE_high
        90.8%
        49%
        0.0
        H3V73AFX2_n01_CD8_CFSE_high_corrected
        99.4%
        49%
        9.6
        H3V73AFX2_n01_CD8_CFSE_low
        92.8%
        49%
        0.0
        H3V73AFX2_n01_CD8_CFSE_low_corrected
        99.4%
        49%
        8.9
        H3V73AFX2_n01_CD8_presort
        96.4%
        49%
        0.1
        H3V73AFX2_n01_CD8_presort_corrected
        99.4%
        49%
        9.8
        H3V73AFX2_n01_CD8_prestim
        78.9%
        49%
        0.0
        H3V73AFX2_n01_CD8_prestim_corrected
        99.4%
        49%
        10.0
        H3V73AFX2_n01_plasmid
        82.7%
        48%
        0.0
        H3V73AFX2_n01_plasmid_corrected
        99.4%
        49%
        8.9
        H3V73AFX2_n01_undetermined
        96.2%
        47%
        14.3

        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 10/10 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        14,323,551
        13.5
        plasmid_corrected
        8,874,429
        8.3
        CD4_prestim_corrected
        11,606,258
        10.9
        CD8_prestim_corrected
        9,963,397
        9.4
        CD4_presort_corrected
        11,485,284
        10.8
        CD8_presort_corrected
        9,803,767
        9.2
        CD4_CFSE_low_corrected
        11,948,325
        11.2
        CD4_CFSE_high_corrected
        9,903,959
        9.3
        CD8_CFSE_low_corrected
        8,873,044
        8.3
        CD8_CFSE_high_corrected
        9,608,928
        9.0

        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
        9675321.0
        67.5
        NNNNNNNN
        248867.0
        1.7
        GATCATGA
        121112.0
        0.8
        CTTACCTA
        115763.0
        0.8
        CCTTACTA
        113769.0
        0.8
        CCTACCTA
        102182.0
        0.7
        ACAAGGAA
        94966.0
        0.7
        TGTAACGA
        92359.0
        0.6
        CTTACTTA
        73416.0
        0.5
        ATACCTTA
        66575.0
        0.5
        CGATATGA
        66138.0
        0.5
        ACGCGCGA
        64123.0
        0.5
        ATACTGTA
        63062.0
        0.4
        CGATCAGA
        62037.0
        0.4
        GGTAACGA
        60270.0
        0.4
        ACCAGGAA
        57855.0
        0.4
        ATCGTGTA
        55872.0
        0.4
        GATCTGTA
        52102.0
        0.4
        CATCATGA
        51918.0
        0.4
        CGATCTGA
        48807.0
        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
        114,604,410
        106,390,942
        13.5
        7.8

        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 (150bp).


        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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