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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 2017-09-07, 01:09 based on data in: /mnt/gencore/sites/core-fastqc.bio.nyu.edu/html/HVTL7BGX2/merged


        General Statistics

        Showing 23/23 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HVTL7BGX2_n01_col_60n_r3
        60.5%
        47%
        5.9
        HVTL7BGX2_n01_cotylset1_01
        59.3%
        43%
        20.5
        HVTL7BGX2_n01_cotylset1_02
        64.0%
        44%
        25.9
        HVTL7BGX2_n01_cotylset1_03
        71.5%
        43%
        46.6
        HVTL7BGX2_n01_cotylset1_04
        63.1%
        43%
        24.3
        HVTL7BGX2_n01_cotylset1_05
        64.7%
        43%
        28.8
        HVTL7BGX2_n01_cotylset1_06
        60.7%
        43%
        21.0
        HVTL7BGX2_n01_cotylset1_07
        61.4%
        44%
        30.4
        HVTL7BGX2_n01_cotylset1_08
        61.9%
        44%
        25.7
        HVTL7BGX2_n01_cotylset1_09
        60.5%
        43%
        16.8
        HVTL7BGX2_n01_cotylset1_10
        66.2%
        43%
        35.7
        HVTL7BGX2_n01_cotylset1_11
        52.3%
        44%
        13.8
        HVTL7BGX2_n01_cotylset1_12
        57.0%
        43%
        14.2
        HVTL7BGX2_n01_cotylset1_13
        62.6%
        43%
        24.0
        HVTL7BGX2_n01_cotylset1_14
        67.5%
        43%
        37.7
        HVTL7BGX2_n01_cotylset1_15
        65.5%
        43%
        32.6
        HVTL7BGX2_n01_cotylset1_16
        64.2%
        43%
        30.2
        HVTL7BGX2_n01_cotylset1_17
        55.0%
        43%
        13.4
        HVTL7BGX2_n01_tga1ox_01n_r3
        68.2%
        47%
        34.4
        HVTL7BGX2_n01_tga1ox_05n_r3
        56.0%
        46%
        11.8
        HVTL7BGX2_n01_tga1ox_10n_r3
        63.5%
        47%
        18.9
        HVTL7BGX2_n01_tga1ox_20n_r3
        50.0%
        45%
        9.3
        HVTL7BGX2_n01_tga1ox_60n_r3
        43.1%
        45%
        6.3

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 3/3 columns.
        Number of LanesTotal # of Single-End ReadsTotal # PF ReadsUndetermined
        4.0
        603992094
        542469169
        2.6%

        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 23/23 rows and 3/3 columns.
        LibraryTotal Read CountPortion (%)Perfect (%)
        cotylset1_12
        14240042
        2.7
        98.5
        cotylset1_17
        13359766
        2.5
        98.8
        tga1ox_01n_r3
        34444361
        6.5
        98.0
        tga1ox_20n_r3
        9343951
        1.8
        98.2
        cotylset1_13
        24041426
        4.5
        98.5
        cotylset1_11
        13785175
        2.6
        98.8
        tga1ox_10n_r3
        18908956
        3.6
        98.5
        cotylset1_07
        30378946
        5.8
        98.6
        col_60n_r3
        5931548
        1.1
        97.8
        cotylset1_09
        16813440
        3.2
        98.7
        cotylset1_08
        25725564
        4.9
        98.7
        cotylset1_03
        46554468
        8.8
        98.8
        cotylset1_16
        30186138
        5.7
        98.5
        tga1ox_05n_r3
        11827683
        2.2
        98.5
        cotylset1_04
        24340102
        4.6
        96.7
        cotylset1_06
        21049760
        4.0
        98.7
        cotylset1_15
        32572511
        6.2
        98.7
        cotylset1_10
        35725789
        6.8
        98.6
        cotylset1_05
        28814631
        5.5
        98.8
        tga1ox_60n_r3
        6250800
        1.2
        98.5
        cotylset1_14
        37669969
        7.1
        98.7
        cotylset1_02
        25916298
        4.9
        98.8
        cotylset1_01
        20494217
        3.9
        98.4

        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.

        No samples found with any adapter contamination > 0.1%