..plots loading..

Highlight Samples

Regex mode off

    Rename Samples

    Click here for bulk input.

    Paste two columns of a tab-delimited table here (eg. from Excel).

    First column should be the old name, second column the new name.

    Regex mode off

      Show / Hide Samples

      Regex mode off

        Export Plots

        px
        px
        X

        Download the raw data used to create the plots in this report below:

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


        Choose Plots

        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

        Save Settings

        You can save the toolbox settings for this report to the browser.


        Load Settings

        Choose a saved report profile from the dropdown box below:

        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 2019-06-18, 06:06 based on data in: /beegfs/mk5636/logs/html/HHJHYBGXB/merged


        General Statistics

        Showing 20/20 rows and 4/5 columns.
        Sample Name% Dups% GCLengthM Seqs
        HHJHYBGXB_n01_Guide
        82.9%
        46%
        28
        16.0
        HHJHYBGXB_n01_HTO_1
        42.1%
        48%
        28
        16.3
        HHJHYBGXB_n01_HTO_2
        41.7%
        48%
        28
        16.7
        HHJHYBGXB_n01_HTO_3
        42.5%
        48%
        28
        16.6
        HHJHYBGXB_n01_HTO_4
        43.2%
        48%
        28
        17.2
        HHJHYBGXB_n01_RNA_1
        3.2%
        47%
        28
        91.6
        HHJHYBGXB_n01_RNA_2
        3.2%
        47%
        28
        92.8
        HHJHYBGXB_n01_RNA_3
        3.7%
        47%
        28
        113.8
        HHJHYBGXB_n01_RNA_4
        3.1%
        47%
        28
        86.2
        HHJHYBGXB_n01_undetermined
        44.9%
        46%
        28
        41.6
        HHJHYBGXB_n02_Guide
        74.4%
        50%
        55
        16.0
        HHJHYBGXB_n02_HTO_1
        91.4%
        49%
        55
        16.3
        HHJHYBGXB_n02_HTO_2
        91.4%
        50%
        55
        16.7
        HHJHYBGXB_n02_HTO_3
        91.5%
        49%
        55
        16.6
        HHJHYBGXB_n02_HTO_4
        91.8%
        50%
        55
        17.2
        HHJHYBGXB_n02_RNA_1
        58.0%
        46%
        55
        91.6
        HHJHYBGXB_n02_RNA_2
        59.5%
        46%
        55
        92.8
        HHJHYBGXB_n02_RNA_3
        58.1%
        46%
        55
        113.8
        HHJHYBGXB_n02_RNA_4
        56.3%
        46%
        55
        86.2
        HHJHYBGXB_n02_undetermined
        70.3%
        64%
        55
        41.6

        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.

        Showing 10/10 rows and 2/2 columns.
        Sample NameTotal Read CountPortion (%)
        undetermined_library
        41,636,008
        8.2
        RNA_1
        91,595,596
        18.0
        RNA_2
        92,778,672
        18.2
        RNA_3
        113,782,238
        22.4
        RNA_4
        86,246,981
        16.9
        Guide
        15,997,335
        3.1
        HTO_1
        16,275,283
        3.2
        HTO_2
        16,744,905
        3.3
        HTO_3
        16,646,631
        3.3
        HTO_4
        17,200,518
        3.4

        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 (%)
        GGGGGGGG
        32061028.0
        77.0
        CTGACTCA
        274252.0
        0.7
        TGGACTCA
        234371.0
        0.6
        TGGGGGGG
        185798.0
        0.5
        GGGTGGGG
        145829.0
        0.3
        AACCTCAA
        125862.0
        0.3
        AAACTCAA
        123686.0
        0.3
        GCCTTGTA
        122483.0
        0.3
        GCCTGGTA
        114164.0
        0.3
        GGGGGCGG
        99230.0
        0.2
        CGGACTCA
        97227.0
        0.2
        CTGGACCA
        89886.0
        0.2
        GCTTGGTA
        88693.0
        0.2
        GCGGGGGG
        84923.0
        0.2
        GCCGGGGG
        81212.0
        0.2
        GGCGGGGG
        73929.0
        0.2
        GCCGGGGT
        71156.0
        0.2
        CTGGATCA
        70285.0
        0.2
        AAACAAAA
        70064.0
        0.2
        AAACCCAA
        66822.0
        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
        558,170,384
        508,904,167
        8.2
        2.7

        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 (28bp , 55bp). See the General Statistics Table.


        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%