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for the input DNA quantitation data, can I use the total read count in each sample?
No. In (almost all) cases, a step happens during library pooling where higher amounts of library product from low-DNA samples are included on the sequencer, with the goal of getting a similar number of reads from all samples. Thus read depth does not correspond to input DNA concentration.
Hi Benjamin,
Thanks for your time on developing and maintaining this package. It is exactly what I need!
I have a metagenomic dataset. My quick question is: for the input DNA quantitation data, can I use the total read count in each sample?
Thanks,
Yuandong
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