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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 2019-02-06, 07:02 based on data in: /beegfs/mk5636/logs/html/HLYLTBGX9/merged


        General Statistics

        Showing 18/18 rows and 4/5 columns.
        Sample Name% Dups% GCLengthM Seqs
        HLYLTBGX9_n01_ADT5n
        18.5%
        48%
        26
        28.2
        HLYLTBGX9_n01_BLG5n
        14.8%
        48%
        26
        36.2
        HLYLTBGX9_n01_GO5n
        97.3%
        50%
        26
        48.7
        HLYLTBGX9_n01_HTO5n
        40.4%
        49%
        26
        27.6
        HLYLTBGX9_n01_cDNA5n_a
        8.8%
        49%
        26
        78.5
        HLYLTBGX9_n01_cDNA5n_b
        13.6%
        49%
        26
        141.8
        HLYLTBGX9_n01_cDNA5n_c
        8.8%
        49%
        26
        78.3
        HLYLTBGX9_n01_cDNA5n_d
        9.2%
        49%
        26
        82.5
        HLYLTBGX9_n01_undetermined
        56.1%
        45%
        26
        21.3
        HLYLTBGX9_n02_ADT5n
        16.5%
        42%
        49
        28.2
        HLYLTBGX9_n02_BLG5n
        13.1%
        46%
        49
        36.2
        HLYLTBGX9_n02_GO5n
        95.9%
        45%
        49
        48.7
        HLYLTBGX9_n02_HTO5n
        37.5%
        44%
        49
        27.6
        HLYLTBGX9_n02_cDNA5n_a
        61.9%
        51%
        49
        78.5
        HLYLTBGX9_n02_cDNA5n_b
        65.4%
        51%
        49
        141.8
        HLYLTBGX9_n02_cDNA5n_c
        62.0%
        51%
        49
        78.3
        HLYLTBGX9_n02_cDNA5n_d
        61.8%
        51%
        49
        82.5
        HLYLTBGX9_n02_undetermined
        62.8%
        48%
        49
        21.3

        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 9/9 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        21,346,684
        3.9
        cDNA5n_a
        78,516,757
        14.5
        cDNA5n_b
        141,832,769
        26.1
        cDNA5n_c
        78,282,268
        14.4
        cDNA5n_d
        82,452,182
        15.2
        ADT5n
        28,247,895
        5.2
        HTO5n
        27,597,023
        5.1
        GO5n
        48,736,394
        9.0
        BLG5n
        36,164,355
        6.7

        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 (%)
        GGGGGGGG
        14050975.0
        65.8
        AAGGTGAA
        125112.0
        0.6
        CTTAATCA
        101814.0
        0.5
        CGTAATCA
        91044.0
        0.4
        TCAACGCT
        90893.0
        0.4
        GCACGCTA
        79666.0
        0.4
        TACTCAGA
        78686.0
        0.4
        ATCACATC
        76346.0
        0.4
        AGGGTGAA
        68879.0
        0.3
        TTACTAGA
        64511.0
        0.3
        TCCGAGAA
        63305.0
        0.3
        CGTTATCA
        61192.0
        0.3
        NNNNNNNN
        59976.0
        0.3
        AGTTAATA
        54673.0
        0.3
        TCCACACA
        54169.0
        0.2
        CACAATCA
        53163.0
        0.2
        GTTAATCA
        51303.0
        0.2
        TTAAACAT
        50264.0
        0.2
        TGTTCGTA
        49652.0
        0.2
        AATTCTGA
        49224.0
        0.2

        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
        624,610,752
        543,176,327
        3.9
        2.0

        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 (49bp , 26bp). 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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