I'm pretty new to working with NGS data . I want to do a classification on sequencing profiles from different body organs. for some tissues I have both single cell and bulk sequencing data and for the rest I only have bulk sequencing data. My question is how to merge single cell and bulk sequencing data? and is this kind of merging usually advised or discouraged?
Question: merging single cell and bulk sequencing data
4 weeks ago by
pegah.taklifi • 0
pegah.taklifi • 0 wrote:
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