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

        Report generated on 2016-05-23, 08:05 based on data in: /root/galaxy/database/jobs_directory/000/87/working/multiqc_WDir


        General Statistics

        Showing 1 rows.
        Sample Name% Dups% GCLengthM Seqs
        poulet5_1
        36.3%
        48%
        101
        0.3

        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 exactly 101 bp in length.


        Sequence Duplication Levels

        The relative level of duplication found for every sequence. See the FastQC help.

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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.

        No samples found with any adapter contamination > 0.1%