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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.

         Loading report..

        Report generated on 2018-04-05, 04:04 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HWV57AFXX/merged


        General Statistics

        Showing 24/24 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HWV57AFXX_n01_ah119c3htop2-0318
        26.1%
        40%
        6.4
        HWV57AFXX_n01_ah119i3h-0318
        21.6%
        38%
        6.5
        HWV57AFXX_n01_ah3988c3hflag-0318
        23.2%
        38%
        8.2
        HWV57AFXX_n01_ah3988i3h-0318
        22.6%
        38%
        7.5
        HWV57AFXX_n01_ah5184c3htop2-spikein-0318
        25.5%
        40%
        6.7
        HWV57AFXX_n01_ah5184i3h-0318
        23.3%
        39%
        8.3
        HWV57AFXX_n01_ah6408a-0318
        23.1%
        39%
        8.1
        HWV57AFXX_n01_ah6408i-0318
        29.7%
        40%
        5.9
        HWV57AFXX_n01_ah7797c0htop2-spikein-0318
        25.3%
        38%
        8.0
        HWV57AFXX_n01_ah7797c3htop2-spikein-0318
        24.7%
        39%
        7.0
        HWV57AFXX_n01_ah7797i0h-0318
        21.7%
        39%
        7.1
        HWV57AFXX_n01_ah7797i3h-0318
        18.8%
        38%
        5.7
        HWV57AFXX_n01_ah8867a-0318
        21.1%
        39%
        7.0
        HWV57AFXX_n01_ah8867b-0318
        20.9%
        39%
        6.4
        HWV57AFXX_n01_ah9012c3hflag-0318
        21.9%
        38%
        7.1
        HWV57AFXX_n01_ah9012i3h-0318
        23.2%
        39%
        7.1
        HWV57AFXX_n01_ah9621c3hflag-0318
        24.5%
        38%
        7.6
        HWV57AFXX_n01_ah9621i3h-0318
        21.9%
        38%
        7.3
        HWV57AFXX_n01_ah9624c3hflag-0318
        22.4%
        38%
        6.6
        HWV57AFXX_n01_ah9624i3h-0318
        22.5%
        39%
        8.0
        HWV57AFXX_n01_ah9767c3htop2-spikein-0318
        25.0%
        40%
        6.0
        HWV57AFXX_n01_ah9767i3h-0318
        20.9%
        39%
        6.7
        HWV57AFXX_n01_ah9847c3hmyc-0318
        24.4%
        38%
        6.1
        HWV57AFXX_n01_ah9847i3h-0318
        20.3%
        38%
        6.9

        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
        229064193
        174999557
        3.9
        0.4

        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 (%)
        ah7797i0h-0318
        7131772
        4.2
        91.8
        ah8867a-0318
        6997058
        4.2
        93.6
        ah9767i3h-0318
        6709235
        4.0
        93.8
        ah119i3h-0318
        6461987
        3.8
        94.0
        ah6408a-0318
        8071917
        4.8
        95.0
        ah9012c3hflag-0318
        7140521
        4.2
        94.6
        ah7797i3h-0318
        5726906
        3.4
        94.5
        ah9767c3htop2-spikein-0318
        5981760
        3.6
        87.6
        ah5184i3h-0318
        8292050
        4.9
        93.8
        ah9621i3h-0318
        7308027
        4.3
        94.6
        ah9621c3hflag-0318
        7602897
        4.5
        91.6
        ah6408i-0318
        5899982
        3.5
        93.5
        ah119c3htop2-0318
        6431070
        3.8
        94.3
        ah3988i3h-0318
        7489384
        4.5
        94.7
        ah5184c3htop2-spikein-0318
        6703398
        4.0
        93.2
        ah7797c0htop2-spikein-0318
        7955063
        4.7
        95.0
        ah3988c3hflag-0318
        8160185
        4.9
        93.7
        ah9624i3h-0318
        7970825
        4.7
        95.1
        ah9847c3hmyc-0318
        6115367
        3.6
        93.6
        ah9624c3hflag-0318
        6613915
        3.9
        94.3
        ah7797c3htop2-spikein-0318
        6973530
        4.1
        94.3
        ah9847i3h-0318
        6903939
        4.1
        93.6
        ah9012i3h-0318
        7068550
        4.2
        94.7
        ah8867b-0318
        6416358
        3.8
        94.0

        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 (100bp).


        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.

        24 samples had less than 1% of reads made up of overrepresented sequences

        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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