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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 2018-01-10, 03:01 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HFG2NBGX5/merged


        General Statistics

        Showing 24/24 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HFG2NBGX5_n01_323h2a
        50.1%
        42%
        12.2
        HFG2NBGX5_n01_323h4
        54.8%
        41%
        27.3
        HFG2NBGX5_n01_655
        54.2%
        39%
        19.2
        HFG2NBGX5_n01_663h2a
        50.8%
        42%
        11.3
        HFG2NBGX5_n01_663h4
        41.2%
        45%
        14.7
        HFG2NBGX5_n01_734h2a
        54.3%
        48%
        16.0
        HFG2NBGX5_n01_734h4
        39.4%
        41%
        11.1
        HFG2NBGX5_n01_768
        8.6%
        44%
        0.0
        HFG2NBGX5_n01_769h2a
        52.0%
        40%
        13.7
        HFG2NBGX5_n01_769h4
        31.0%
        39%
        12.2
        HFG2NBGX5_n01_770h2a
        42.5%
        39%
        13.2
        HFG2NBGX5_n01_770h4
        32.1%
        40%
        12.8
        HFG2NBGX5_n01_771
        56.4%
        40%
        18.3
        HFG2NBGX5_n01_772
        51.7%
        39%
        17.5
        HFG2NBGX5_n01_773h2a
        49.9%
        40%
        13.7
        HFG2NBGX5_n01_773h4
        31.1%
        39%
        11.3
        HFG2NBGX5_n01_775
        50.9%
        39%
        15.9
        HFG2NBGX5_n01_777h2a
        48.2%
        40%
        16.4
        HFG2NBGX5_n01_777h4
        29.0%
        39%
        12.2
        HFG2NBGX5_n01_778h2a
        45.8%
        40%
        11.7
        HFG2NBGX5_n01_778h4
        33.0%
        39%
        14.5
        HFG2NBGX5_n01_779
        53.6%
        40%
        16.1
        HFG2NBGX5_n01_785
        55.9%
        41%
        15.7
        HFG2NBGX5_n01_796
        57.5%
        41%
        17.3

        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
        380531362
        361086204
        4.6
        2.4

        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 (%)
        785.0
        15743609
        4.6
        98.9
        770h2a
        13237784
        3.8
        98.7
        323h4
        27317759
        7.9
        98.0
        768.0
        24202
        0.0
        0.8
        663h2a
        11290239
        3.3
        98.6
        796.0
        17280804
        5.0
        98.6
        778h2a
        11662395
        3.4
        98.9
        734h2a
        16021582
        4.7
        97.9
        771.0
        18266232
        5.3
        99.0
        770h4
        12822173
        3.7
        98.8
        772.0
        17525954
        5.1
        97.9
        778h4
        14463979
        4.2
        98.4
        773h2a
        13721801
        4.0
        98.5
        769h2a
        13710057
        4.0
        98.8
        734h4
        11134312
        3.2
        98.6
        777h4
        12223579
        3.5
        98.8
        777h2a
        16417000
        4.8
        98.5
        655.0
        19177969
        5.6
        98.9
        773h4
        11322404
        3.3
        98.8
        323h2a
        12211049
        3.5
        98.4
        775.0
        15868062
        4.6
        98.9
        779.0
        16081583
        4.7
        97.6
        769h4
        12210213
        3.5
        98.9
        663h4
        14661697
        4.3
        98.5

        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..