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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 2017-06-08, 22:06 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HMY52BGX2/merged


        General Statistics

        Showing 26/26 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HMY52BGX2_n01_jes_1
        43.7%
        45%
        10.2
        HMY52BGX2_n01_jes_109
        41.8%
        45%
        9.3
        HMY52BGX2_n01_jes_110
        46.3%
        45%
        11.2
        HMY52BGX2_n01_jes_111
        43.8%
        45%
        11.1
        HMY52BGX2_n01_jes_121
        46.0%
        45%
        11.0
        HMY52BGX2_n01_jes_122
        43.6%
        45%
        10.2
        HMY52BGX2_n01_jes_123
        58.7%
        45%
        24.8
        HMY52BGX2_n01_jes_3
        44.5%
        45%
        10.1
        HMY52BGX2_n01_protest_01
        28.4%
        46%
        1.6
        HMY52BGX2_n01_protest_02
        33.8%
        47%
        2.5
        HMY52BGX2_n01_protest_03
        28.7%
        46%
        1.4
        HMY52BGX2_n01_protest_04
        31.6%
        47%
        1.9
        HMY52BGX2_n01_protest_05
        38.4%
        47%
        2.8
        HMY52BGX2_n01_protest_06
        30.2%
        47%
        1.7
        HMY52BGX2_n01_protest_07
        32.6%
        46%
        2.7
        HMY52BGX2_n01_protest_08
        37.7%
        47%
        3.5
        HMY52BGX2_n01_protest_09
        45.0%
        46%
        7.7
        HMY52BGX2_n01_protest_10
        34.9%
        47%
        2.9
        HMY52BGX2_n01_protest_11
        31.3%
        46%
        2.0
        HMY52BGX2_n01_protest_12
        30.0%
        47%
        1.4
        HMY52BGX2_n01_protest_13
        38.0%
        46%
        4.9
        HMY52BGX2_n01_protest_14
        40.3%
        47%
        5.0
        HMY52BGX2_n01_protest_15
        32.5%
        46%
        2.4
        HMY52BGX2_n01_protest_16
        38.4%
        47%
        4.1
        HMY52BGX2_n01_protest_17
        38.2%
        46%
        4.5
        HMY52BGX2_n01_protest_18
        38.3%
        47%
        2.8

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 3/3 columns.
        Number of LanesTotal # of Single-End ReadsTotal # PF ReadsUndetermined
        4.0
        168794587
        165631382
        1.89%

        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 26/26 rows and 3/3 columns.
        LibraryTotal Read CountPortion (%)Perfect (%)
        jes_1
        10187327
        6.6
        98.4
        protest_13
        4874070
        3.2
        99.0
        jes_123
        24815065
        16.1
        99.0
        protest_08
        3476062
        2.3
        98.8
        protest_12
        1403856
        0.9
        98.3
        protest_07
        2739538
        1.8
        98.5
        protest_03
        1386618
        0.9
        98.8
        protest_02
        2492836
        1.6
        98.8
        jes_109
        9346671
        6.1
        98.8
        protest_01
        1615031
        1.1
        98.8
        protest_18
        2814312
        1.8
        98.7
        jes_122
        10176481
        6.6
        98.8
        jes_111
        11130113
        7.2
        98.9
        protest_10
        2872894
        1.9
        98.7
        protest_06
        1663702
        1.1
        98.8
        protest_11
        1955449
        1.3
        98.5
        jes_3
        10056185
        6.5
        98.9
        protest_04
        1915339
        1.2
        98.1
        protest_16
        4139355
        2.7
        98.6
        protest_15
        2388073
        1.6
        97.9
        protest_09
        7724289
        5.0
        98.9
        jes_110
        11226659
        7.3
        98.9
        protest_05
        2755247
        1.8
        98.6
        jes_121
        11013976
        7.2
        98.7
        protest_14
        4978649
        3.2
        98.6
        protest_17
        4544682
        3.0
        98.8

        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.

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        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.

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        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.

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        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.

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