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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 2017-12-20, 18:12 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HW22FAFXX/merged


        General Statistics

        Showing 24/24 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HW22FAFXX_n01_vs10_171213
        24.8%
        38%
        7.2
        HW22FAFXX_n01_vs11_171213
        21.9%
        38%
        6.5
        HW22FAFXX_n01_vs12_171213
        20.2%
        38%
        5.4
        HW22FAFXX_n01_vs13_171213
        22.9%
        38%
        5.6
        HW22FAFXX_n01_vs14_171213
        25.8%
        37%
        5.3
        HW22FAFXX_n01_vs15_171213
        23.2%
        38%
        6.6
        HW22FAFXX_n01_vs16_171213
        34.6%
        37%
        10.7
        HW22FAFXX_n01_vs17_171213
        22.1%
        37%
        5.8
        HW22FAFXX_n01_vs18_171213
        31.2%
        37%
        6.4
        HW22FAFXX_n01_vs19_171213
        23.5%
        38%
        7.3
        HW22FAFXX_n01_vs1_171213
        27.5%
        38%
        7.7
        HW22FAFXX_n01_vs20_171213
        26.5%
        38%
        7.1
        HW22FAFXX_n01_vs21_171213
        25.4%
        38%
        7.9
        HW22FAFXX_n01_vs22_171213
        25.4%
        38%
        7.5
        HW22FAFXX_n01_vs23_171213
        24.8%
        38%
        7.8
        HW22FAFXX_n01_vs24_171213
        39.4%
        37%
        8.2
        HW22FAFXX_n01_vs2_171213
        30.8%
        38%
        7.0
        HW22FAFXX_n01_vs3_171213
        25.7%
        39%
        6.9
        HW22FAFXX_n01_vs4_171213
        31.2%
        38%
        6.0
        HW22FAFXX_n01_vs5_171213
        23.0%
        38%
        6.7
        HW22FAFXX_n01_vs6_171213
        24.9%
        37%
        6.3
        HW22FAFXX_n01_vs7_171213
        22.3%
        38%
        6.0
        HW22FAFXX_n01_vs8_171213
        27.6%
        37%
        7.2
        HW22FAFXX_n01_vs9_171213
        25.4%
        38%
        9.1

        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
        195900540
        174114787
        3.5
        1.1

        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 (%)
        vs23_171213
        7788437
        4.6
        98.0
        vs5_171213
        6650264
        4.0
        96.2
        vs13_171213
        5599441
        3.3
        96.2
        vs10_171213
        7202024
        4.3
        97.4
        vs18_171213
        6446709
        3.8
        97.5
        vs6_171213
        6304641
        3.8
        97.8
        vs22_171213
        7506989
        4.5
        97.8
        vs20_171213
        7100643
        4.2
        97.7
        vs2_171213
        7020863
        4.2
        94.3
        vs17_171213
        5842235
        3.5
        97.6
        vs9_171213
        9074890
        5.4
        97.6
        vs24_171213
        8222677
        4.9
        98.0
        vs1_171213
        7656136
        4.6
        97.5
        vs19_171213
        7345697
        4.4
        97.6
        vs4_171213
        5994466
        3.6
        97.4
        vs14_171213
        5258769
        3.1
        97.7
        vs15_171213
        6552043
        3.9
        97.5
        vs8_171213
        7171452
        4.3
        98.0
        vs7_171213
        5953428
        3.5
        97.5
        vs11_171213
        6507088
        3.9
        96.9
        vs16_171213
        10669766
        6.4
        97.8
        vs12_171213
        5355225
        3.2
        97.6
        vs3_171213
        6889082
        4.1
        97.9
        vs21_171213
        7862483
        4.7
        98.0

        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 (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.

        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.

        No samples found with any adapter contamination > 0.1%