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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.

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        Report generated on 2017-11-15, 19:11 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HVH7LAFXX/merged


        General Statistics

        Showing 24/24 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HVH7LAFXX_n01_vs10_171115
        33.2%
        38%
        8.3
        HVH7LAFXX_n01_vs11_171115
        25.4%
        39%
        7.4
        HVH7LAFXX_n01_vs12_171115
        27.2%
        37%
        5.5
        HVH7LAFXX_n01_vs13_171115
        28.4%
        37%
        6.2
        HVH7LAFXX_n01_vs14_171115
        38.9%
        37%
        8.0
        HVH7LAFXX_n01_vs15_171115
        32.7%
        38%
        9.6
        HVH7LAFXX_n01_vs16_171115
        41.0%
        38%
        9.6
        HVH7LAFXX_n01_vs17_171115
        27.4%
        38%
        7.1
        HVH7LAFXX_n01_vs18_171115
        32.0%
        38%
        7.8
        HVH7LAFXX_n01_vs19_171115
        26.3%
        38%
        6.8
        HVH7LAFXX_n01_vs1_171115
        25.2%
        38%
        6.4
        HVH7LAFXX_n01_vs20_171115
        31.9%
        37%
        6.7
        HVH7LAFXX_n01_vs21_171115
        27.0%
        38%
        7.9
        HVH7LAFXX_n01_vs22_171115
        36.9%
        38%
        11.4
        HVH7LAFXX_n01_vs23_171115
        26.5%
        38%
        8.0
        HVH7LAFXX_n01_vs24_171115
        28.7%
        37%
        5.2
        HVH7LAFXX_n01_vs2_171115
        28.3%
        38%
        6.5
        HVH7LAFXX_n01_vs3_171115
        28.7%
        38%
        8.2
        HVH7LAFXX_n01_vs4_171115
        30.2%
        38%
        6.8
        HVH7LAFXX_n01_vs5_171115
        27.5%
        38%
        7.4
        HVH7LAFXX_n01_vs6_171115
        30.4%
        38%
        7.1
        HVH7LAFXX_n01_vs7_171115
        30.7%
        38%
        9.1
        HVH7LAFXX_n01_vs8_171115
        31.7%
        38%
        7.3
        HVH7LAFXX_n01_vs9_171115
        25.3%
        39%
        6.7

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 4/4 columns.
        Number of LanesTotal # of Single-End ReadsTotal # PF ReadsUndetermined % PhiX Aligned
        4.0
        212236086
        186448216
        3.0
        0.71%

        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.
        Perfect: The percentage of reads in this library which have a barcode perfectly matching the barcode specified in TuboWeb. The remainder of reads have mismatches upto the max number of mismatches specified in TuboWeb (Allowed barcode mismatch option in your Library Pool).

        Showing 24/24 rows and 3/3 columns.
        LibraryTotal Read CountPortion (%)Perfect (%)
        vs7_171115
        9118516
        5.0
        97.6
        vs16_171115
        9587629
        5.3
        97.8
        vs11_171115
        7441199
        4.1
        97.1
        vs14_171115
        7999388
        4.4
        97.8
        vs8_171115
        7315032
        4.0
        97.9
        vs9_171115
        6713359
        3.7
        97.5
        vs6_171115
        7051794
        3.9
        97.6
        vs23_171115
        8014269
        4.4
        98.1
        vs24_171115
        5199143
        2.9
        97.8
        vs18_171115
        7774028
        4.3
        97.4
        vs10_171115
        8264776
        4.6
        97.4
        vs21_171115
        7888903
        4.4
        98.1
        vs19_171115
        6838949
        3.8
        97.7
        vs12_171115
        5522417
        3.1
        97.6
        vs2_171115
        6514071
        3.6
        93.7
        vs4_171115
        6758043
        3.7
        97.3
        vs22_171115
        11350468
        6.3
        98.0
        vs1_171115
        6449624
        3.6
        97.5
        vs17_171115
        7062646
        3.9
        97.7
        vs20_171115
        6687726
        3.7
        97.6
        vs13_171115
        6199096
        3.4
        96.1
        vs5_171115
        7352059
        4.1
        96.1
        vs3_171115
        8154970
        4.5
        97.9
        vs15_171115
        9615114
        5.3
        97.7

        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.

        loading..

        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.

        loading..

        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.

        loading..

        Per Base N Content

        The percentage of base calls at each position for which an N was called. See the FastQC help.

        loading..

        Sequence Length Distribution

        All samples have sequences of a single length (50bp).


        Sequence Duplication Levels

        The relative level of duplication found for every sequence. See the FastQC help.

        loading..

        Overrepresented sequences

        The total amount of overrepresented sequences found in each library. See the FastQC help for further information.

        loading..

        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%