If not an error, choose a category for your question(REQUIRED):
a) Will using GenomeSTRiP to analyze different datasets in terms of coverage, read-base pairs, PCR vs PCR-free, affect the results I will get?
I am trying to run an analysis on a cohort that has samples with different sequencing depth (30X and >30X), some are PCR free and some I'm unsure if they PCR free, some samples have a read length of 150bp and some 100bp. I want to find out if GenomeSTRiP will have problems processing this type of dataset? Or will the read length and depth affect the results? I am using whole-genome sequencing data.
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