FeatureCounts MultiQC

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        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 1.11

        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

        FeatureCounts MultiQC

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

        Report generated on 2022-05-10, 12:53 based on data in: /mnt/tmp/job_working_directory/004/028/4028371/working/multiqc_WDir


        General Statistics

        Showing 6/6 rows and 2/2 columns.
        Sample Name% AssignedM Assigned
        HISAT2 on data 25: aligned reads (BAM)
        72.4%
        2.6
        HISAT2 on data 27: aligned reads (BAM)
        72.4%
        2.6
        HISAT2 on data 29: aligned reads (BAM)
        72.4%
        2.6
        HISAT2 on data 31: aligned reads (BAM)
        79.0%
        6.4
        HISAT2 on data 33: aligned reads (BAM)
        78.9%
        6.4
        HISAT2 on data 35: aligned reads (BAM)
        79.0%
        6.4

        featureCounts

        Subread featureCounts is a highly efficient general-purpose read summarization program that counts mapped reads for genomic features such as genes, exons, promoter, gene bodies, genomic bins and chromosomal locations.

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