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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 2020-09-11, 04:09 based on data in: /beegfs/mk5636/logs/html/000000000-G69NV/1


        General Statistics

        Showing 14/14 rows and 4/5 columns.
        Sample Name% Dups% GCLengthM Seqs
        000000000-G69NV_l01_n01_JRS_018_C8A
        54.0%
        46%
        28
        0.9
        000000000-G69NV_l01_n01_JRS_018_C8C
        53.5%
        46%
        28
        0.9
        000000000-G69NV_l01_n01_JRS_018_C8G
        68.6%
        47%
        28
        0.3
        000000000-G69NV_l01_n01_JRS_018_C8T
        68.2%
        46%
        28
        0.6
        000000000-G69NV_l01_n01_JRS_018_C9A
        69.4%
        47%
        28
        0.2
        000000000-G69NV_l01_n01_JRS_018_C9T
        68.3%
        47%
        28
        0.3
        000000000-G69NV_l01_n01_undetermined
        94.1%
        44%
        28
        0.9
        000000000-G69NV_l01_n02_JRS_018_C8A
        89.6%
        46%
        287
        0.9
        000000000-G69NV_l01_n02_JRS_018_C8C
        85.6%
        44%
        287
        0.9
        000000000-G69NV_l01_n02_JRS_018_C8G
        95.5%
        51%
        287
        0.3
        000000000-G69NV_l01_n02_JRS_018_C8T
        85.4%
        46%
        287
        0.6
        000000000-G69NV_l01_n02_JRS_018_C9A
        92.2%
        50%
        287
        0.2
        000000000-G69NV_l01_n02_JRS_018_C9T
        93.3%
        50%
        287
        0.3
        000000000-G69NV_l01_n02_undetermined
        93.1%
        44%
        287
        0.9

        Lane 1 Demultiplexing Report

        Lane 1 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 7/7 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        949,047
        22.9
        JRS_018_C8A
        881,777
        21.3
        JRS_018_C8T
        591,700
        14.3
        JRS_018_C8C
        914,196
        22.1
        JRS_018_C8G
        337,119
        8.1
        JRS_018_C9A
        156,561
        3.8
        JRS_018_C9T
        307,854
        7.4

        Barcodes of Undetermined Reads

        Barcodes of Undetermined Reads
        We have determined the barcodes of your undetermined reads (reads containing a barcode that you did not encode in your metadata). Here are the top 20 barcodes belonging to the undetermined reads. The full list is available here.

        Showing 20/20 rows and 2/2 columns.
        Sample NameCountFrequency (%)
        CTCTCTCT
        30778.0
        3.2
        TTTCTCCC
        10258.0
        1.1
        CTCTATCT
        10233.0
        1.1
        CCCTCTCT
        9504.0
        1.0
        CCCCTTTC
        7707.0
        0.8
        TTTTCCTC
        7236.0
        0.8
        ACCCTTGC
        7210.0
        0.8
        CTCTCCCT
        6116.0
        0.6
        CTCTCGCT
        5172.0
        0.5
        CTCGCTCT
        4946.0
        0.5
        TCTTCCCT
        4596.0
        0.5
        TCTCTCCC
        3690.0
        0.4
        CTCCCTCT
        3361.0
        0.3
        TCTTCTTT
        3088.0
        0.3
        CTCACTCT
        3081.0
        0.3
        TTTTCCTT
        2987.0
        0.3
        CTCCATCT
        2882.0
        0.3
        CCCCTTCC
        2847.0
        0.3
        TTTTCCTA
        2781.0
        0.3
        TCTCCCTC
        2696.0
        0.3

        Lane Statistics

        Lane Statistics

        Showing 1/1 rows and 4/4 columns.
        Sample NameTotal # of Single-End ReadsTotal # PF Reads% Undetermined% PhiX Aligned
        1.0
        4,407,711
        4,138,254
        22.9
        28.0

        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.

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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 (28bp , 287bp). See the General Statistics Table.


        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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