Imagine in your RNASEQ workflow , you align each pair (R1/R2) with STAR ... and finally you concat your intermediate bam into only one for your sample. Usually, multiqc assume you have concat all your R1 and R2 fastq reads and you finally align once with STAR giving you only one _Log.final.out for your sample per dir.
Or if you align each pair (R1/R2) with STAR ... and finally concat in one bam ... your directory you will have several _Log.final.out whereas you treat only one sample. MultiQC will plot ever intermediate pair alignment for each _Log.final.out . Is this possible to tell MultiQC to sum up values from each _Log.final.out and plot only bar for the sample.