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


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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.

        Report generated on 2018-11-15, 00:11 based on data in: /beegfs/mk5636/logs/html/HFKVNBGX9/merged


        General Statistics

        Showing 29/29 rows and 3/5 columns.
        Sample Name% Dups% GCM Seqs
        HFKVNBGX9_n01_NCR6_001
        76.1%
        48%
        14.8
        HFKVNBGX9_n01_NCR6_002
        70.6%
        48%
        13.9
        HFKVNBGX9_n01_NCR6_003
        76.1%
        49%
        9.8
        HFKVNBGX9_n01_NCR6_004
        77.6%
        48%
        12.9
        HFKVNBGX9_n01_NCR6_005
        74.9%
        49%
        11.7
        HFKVNBGX9_n01_NCR6_006
        78.2%
        49%
        15.4
        HFKVNBGX9_n01_NCR6_008
        82.3%
        49%
        15.8
        HFKVNBGX9_n01_NCR6_009
        93.7%
        49%
        12.6
        HFKVNBGX9_n01_NCR6_019
        91.0%
        48%
        9.4
        HFKVNBGX9_n01_NCR6_020
        89.6%
        49%
        7.2
        HFKVNBGX9_n01_NCR6_021
        90.6%
        48%
        8.2
        HFKVNBGX9_n01_NCR6_022
        94.6%
        49%
        9.0
        HFKVNBGX9_n01_NCR6_023
        93.1%
        49%
        10.0
        HFKVNBGX9_n01_NCR6_024
        94.3%
        49%
        13.4
        HFKVNBGX9_n01_NCR6_028
        83.1%
        47%
        9.3
        HFKVNBGX9_n01_NCR6_029
        91.2%
        47%
        10.8
        HFKVNBGX9_n01_NCR6_030
        85.0%
        47%
        9.9
        HFKVNBGX9_n01_NCR6_114
        59.0%
        51%
        14.0
        HFKVNBGX9_n01_NCR6_115
        45.2%
        47%
        15.6
        HFKVNBGX9_n01_NCR6_116
        35.2%
        51%
        12.3
        HFKVNBGX9_n01_NCR6_117
        34.9%
        42%
        12.9
        HFKVNBGX9_n01_NCR6_118
        48.5%
        54%
        7.9
        HFKVNBGX9_n01_NCR6_119
        44.2%
        49%
        8.5
        HFKVNBGX9_n01_NCR6_120
        39.1%
        47%
        5.2
        HFKVNBGX9_n01_NCR6_121
        35.0%
        43%
        9.7
        HFKVNBGX9_n01_NCR6_122
        30.2%
        41%
        9.9
        HFKVNBGX9_n01_NCR6_123
        28.6%
        42%
        4.6
        HFKVNBGX9_n01_NCR6_124
        47.4%
        49%
        5.4
        HFKVNBGX9_n01_undetermined
        70.3%
        49%
        16.8

        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.

        Showing 29/29 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        16,827,216
        5.3
        NCR6_001
        14,840,267
        4.7
        NCR6_002
        13,934,817
        4.4
        NCR6_003
        9,819,715
        3.1
        NCR6_004
        12,865,850
        4.1
        NCR6_005
        11,695,873
        3.7
        NCR6_006
        15,371,408
        4.8
        NCR6_008
        15,801,431
        5.0
        NCR6_009
        12,606,824
        4.0
        NCR6_019
        9,428,389
        3.0
        NCR6_020
        7,230,327
        2.3
        NCR6_021
        8,173,603
        2.6
        NCR6_022
        9,029,005
        2.8
        NCR6_023
        9,992,739
        3.2
        NCR6_024
        13,378,280
        4.2
        NCR6_028
        9,281,165
        2.9
        NCR6_029
        10,803,745
        3.4
        NCR6_030
        9,928,872
        3.1
        NCR6_114
        14,014,625
        4.4
        NCR6_115
        15,623,669
        4.9
        NCR6_116
        12,308,028
        3.9
        NCR6_117
        12,921,846
        4.1
        NCR6_118
        7,885,835
        2.5
        NCR6_119
        8,533,440
        2.7
        NCR6_120
        5,224,473
        1.6
        NCR6_121
        9,696,973
        3.1
        NCR6_122
        9,930,275
        3.1
        NCR6_123
        4,571,384
        1.4
        NCR6_124
        5,402,717
        1.7

        Run Statistics

        Run Statistics

        Showing 1/1 rows and 4/4 columns.
        Sample NameTotal # of Single-End ReadsTotal # PF Reads% Undetermined % PhiX Aligned
        4.0
        337,422,688
        317,122,791
        5.3
        2.3

        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.

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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.

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        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 (76bp).


        Sequence Duplication Levels

        The relative level of duplication found for every sequence. See the FastQC help.

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        Overrepresented sequences

        The total amount of overrepresented sequences found in each library. See the FastQC help for further information.

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        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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