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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 2020-09-29, 08:09 based on data in: /beegfs/mk5636/logs/html/HVC5JBGXG/merged


        General Statistics

        Showing 15/15 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HVC5JBGXG_n01_0920_CD4_CD_high
        99.8%
        49%
        14.3
        HVC5JBGXG_n01_0920_CD4_CD_low
        99.8%
        50%
        23.4
        HVC5JBGXG_n01_0920_CD4_CFSE_high_1
        99.8%
        49%
        10.6
        HVC5JBGXG_n01_0920_CD4_CFSE_high_2
        82.8%
        50%
        0.0
        HVC5JBGXG_n01_0920_CD4_CFSE_low_1
        99.9%
        49%
        17.1
        HVC5JBGXG_n01_0920_CD4_CFSE_low_2
        99.8%
        48%
        18.3
        HVC5JBGXG_n01_0920_CD4_presort
        99.9%
        49%
        25.5
        HVC5JBGXG_n01_0920_CD4_prestim
        99.9%
        48%
        17.6
        HVC5JBGXG_n01_0920_CD8_CD_high
        99.9%
        48%
        23.4
        HVC5JBGXG_n01_0920_CD8_CD_low
        99.8%
        48%
        17.2
        HVC5JBGXG_n01_0920_CD8_CFSE_high
        99.8%
        47%
        17.2
        HVC5JBGXG_n01_0920_CD8_CFSE_low
        99.8%
        48%
        19.0
        HVC5JBGXG_n01_0920_CD8_presort
        99.8%
        48%
        19.5
        HVC5JBGXG_n01_0920_CD8_prestim
        99.8%
        48%
        12.4
        HVC5JBGXG_n01_undetermined
        97.7%
        46%
        36.9

        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 15/15 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        36,921,090
        13.6
        0920_CD4_prestim
        17,582,360
        6.5
        0920_CD8_prestim
        12,383,669
        4.5
        0920_CD4_CFSE_low_1
        17,064,784
        6.3
        0920_CD4_CFSE_high_1
        10,631,421
        3.9
        0920_CD8_CFSE_low
        19,017,053
        7.0
        0920_CD8_CFSE_high
        17,183,047
        6.3
        0920_CD4_CD_low
        23,355,546
        8.6
        0920_CD4_CD_high
        14,290,225
        5.2
        0920_CD8_CD_low
        17,184,647
        6.3
        0920_CD8_CD_high
        23,417,452
        8.6
        0920_CD4_presort
        25,462,633
        9.4
        0920_CD8_presort
        19,470,975
        7.2
        0920_CD4_CFSE_low_2
        18,269,383
        6.7
        0920_CD4_CFSE_high_2
        157.0
        0.0

        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 (%)
        TAACAATGGGGGGGGG
        436233.0
        1.2
        GATCGATAGGGGGGGG
        282237.0
        0.8
        ACGATCGAGGGGGGGG
        254890.0
        0.7
        ATCGATTCGGGGGGGG
        241602.0
        0.7
        GATAGGTCGGGGGGGG
        233925.0
        0.6
        CGATCGATGGGGGGGG
        227284.0
        0.6
        CGATCGATCATTGTTA
        223205.0
        0.6
        GATCGATACCTTACTA
        204073.0
        0.6
        ACGATCGACTTACTTA
        201217.0
        0.5
        GATCGATACTTACCTA
        195520.0
        0.5
        CGATCGATCCATGTTA
        183365.0
        0.5
        GATCGATACCTACCTA
        176275.0
        0.5
        ATACTGTAGGGGGGGG
        158769.0
        0.4
        ATCGATTCCTTACTTA
        141345.0
        0.4
        TAACAATGTGTAACGA
        140126.0
        0.4
        ACGATCGACCTACTTA
        125519.0
        0.3
        ACGATCGACTCACTTA
        123079.0
        0.3
        ATACTGTAACAAGGAA
        117528.0
        0.3
        CGATCGATCCATTTTA
        106291.0
        0.3
        GATAGGTCAATCGTTA
        100320.0
        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
        287,107,056
        272,234,442
        13.6
        9.3

        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 (151bp).


        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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