Loading report..

Toolbox

MultiQC Toolbox

Highlight Samples
    Rename Samples

    Paste two columns of a tab-delimited table here (eg. from Excel). First column should be the old name, second column the new name.

      Show / Hide Samples
        Explain with AI

        Configure AI settings to get explanations of plots and data in this report.

        Keys entered here will be stored in your browser's local storage. See the docs.
        Switch out sample names with random identifiers
        Export Plots
        px
        px
        X
        Note: 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
        Report settings are automatically saved in your browser as you use the toolbox. You can also save named configurations below.
        Load Settings

        Choose a saved report profile from the browser or load from a file:

        Tool Citations

        Please remember to cite all of the tools that you use in your analysis.

        About MultiQC

        This report was generated using MultiQC, version 1.35

        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

        MultiQC is developed by Seqera.

        Scroll to top

        A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.

        Report generated on 2026-05-28, 10:50 CST based on data in: /home/kyhan/test/rna-seq/yeast-standard-out/03_results/count

        General Statistics

        Showing 24/24 rows and 1/2 columns.
        Sample NameAssignedAssigned
        SNF2KO_01
        0.4M
        64.0%
        SNF2KO_02
        0.3M
        54.5%
        SNF2KO_03
        0.4M
        64.0%
        SNF2KO_04
        0.3M
        48.7%
        SNF2KO_05
        0.3M
        61.7%
        SNF2KO_06
        0.4M
        62.6%
        SNF2KO_07
        0.3M
        62.2%
        SNF2KO_08
        0.3M
        57.9%
        SNF2KO_09
        0.4M
        62.8%
        SNF2KO_10
        0.4M
        62.9%
        SNF2KO_11
        0.3M
        62.5%
        SNF2KO_12
        0.4M
        64.3%
        WT_01
        0.3M
        58.7%
        WT_02
        0.3M
        57.7%
        WT_03
        0.3M
        57.8%
        WT_04
        0.3M
        59.6%
        WT_05
        0.3M
        58.7%
        WT_06
        0.4M
        61.2%
        WT_07
        0.3M
        59.2%
        WT_08
        0.3M
        57.0%
        WT_09
        0.3M
        57.5%
        WT_10
        0.3M
        51.7%
        WT_11
        0.3M
        54.3%
        WT_12
        0.3M
        58.0%
        Expand table

        featureCounts

        Counts mapped reads for genomic features such as genes, exons, promoter, gene bodies, genomic bins and chromosomal locations.http://subread.sourceforge.netDOI: 10.1093/bioinformatics/btt656

        Assignments

        Created with MultiQC