Loading report..

Highlight Samples

Regex mode off

    Rename Samples

    Click here for bulk input.

    Paste two columns of a tab-delimited table here (eg. from Excel).

    First column should be the old name, second column the new name.

    Regex mode off

      Show / Hide Samples

      Regex mode off

        Export Plots

        px
        px
        X

        Download the raw data used to create the plots in this report below:

        Note that additional data was saved in multiqc_data when this report was generated.


        Choose Plots

        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

        Save Settings

        You can save the toolbox settings for this report to the browser.


        Load Settings

        Choose a saved report profile from the dropdown box below:

        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 2018-03-13, 15:03 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HMCN3BGX5/merged


        General Statistics

        Showing 19/19 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HMCN3BGX5_n01_damid_mdexbz1
        47.7%
        50%
        1.5
        HMCN3BGX5_n01_damid_mdexdamgr
        51.8%
        49%
        2.0
        HMCN3BGX5_n01_damid_pdexbz1
        59.4%
        52%
        4.1
        HMCN3BGX5_n01_damid_pdexdamgr
        60.9%
        52%
        4.2
        HMCN3BGX5_n01_nxtshoot2_01
        75.5%
        47%
        26.5
        HMCN3BGX5_n01_nxtshoot2_02
        84.8%
        47%
        22.9
        HMCN3BGX5_n01_nxtshoot2_03
        83.6%
        47%
        21.0
        HMCN3BGX5_n01_nxtshoot2_04
        79.3%
        47%
        20.8
        HMCN3BGX5_n01_nxtshoot2_05
        74.6%
        46%
        25.2
        HMCN3BGX5_n01_nxtshoot2_06
        78.4%
        47%
        15.1
        HMCN3BGX5_n01_nxtshoot2_07
        86.7%
        47%
        23.9
        HMCN3BGX5_n01_nxtshoot2_08
        84.7%
        47%
        21.6
        HMCN3BGX5_n01_nxtshoot2_09
        82.8%
        47%
        15.3
        HMCN3BGX5_n01_nxtshoot2_10
        78.6%
        46%
        25.0
        HMCN3BGX5_n01_nxtshoot2_11
        93.4%
        45%
        9.4
        HMCN3BGX5_n01_nxtshoot2_12
        78.4%
        47%
        18.8
        HMCN3BGX5_n01_nxtshoot2_13
        84.4%
        46%
        17.7
        HMCN3BGX5_n01_nxtshoot2_14
        85.2%
        48%
        20.8
        HMCN3BGX5_n01_nxtshoot2_15
        75.9%
        46%
        18.5

        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
        342093441
        324523404
        3.2
        1.6

        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 19/19 rows and 3/3 columns.
        LibraryTotal Read CountPortion (%)Perfect (%)
        nxtshoot2_10
        25017903
        8.0
        84.3
        nxtshoot2_11
        9371944
        3.0
        84.1
        nxtshoot2_03
        20955758
        6.7
        84.2
        damid_mdexbz1
        1493219
        0.5
        78.4
        nxtshoot2_02
        22912611
        7.3
        84.3
        nxtshoot2_01
        26462236
        8.4
        84.3
        nxtshoot2_05
        25180764
        8.0
        84.3
        nxtshoot2_07
        23919287
        7.6
        79.1
        damid_mdexdamgr
        1952198
        0.6
        78.3
        nxtshoot2_09
        15256884
        4.9
        84.2
        nxtshoot2_04
        20803634
        6.6
        84.4
        nxtshoot2_06
        15066844
        4.8
        84.4
        damid_pdexdamgr
        4239614
        1.4
        78.7
        damid_pdexbz1
        4128854
        1.3
        78.6
        nxtshoot2_08
        21593416
        6.9
        79.0
        nxtshoot2_14
        20763708
        6.6
        84.3
        nxtshoot2_12
        18786330
        6.0
        84.2
        nxtshoot2_13
        17705649
        5.6
        84.1
        nxtshoot2_15
        18500881
        5.9
        84.3

        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.

        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 (75bp).


        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.

        loading..