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Could I please ask for a bit more information on the function of the base value - what it does and what impact higher or lower values will have, and correspondingly how I should decide a setting based on the structure of my dataset?
For extra information, my RNAseq dataset is comprised of multiple tissues from various heterozygous individuals. I intend to conduct a multiple-k approach - should I run ORNA separate times with different values of k on the dataset to generate a set of normalised reads for respective assembly run, or should a single normalisation using the smallest k suffice?
Best wishes,
Reza
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