In single-cell RNAseq, when we use any pseudotime/ trajectory analysis it gives us cellular physiological state. Is it possible to stack a heterogeneous population into an order of there development in that particular treatment? To further expand on the question- I have one sample diseased vs one control so I want to see how cells are developed to give rise to disease. In most cases, we have to assign one cell type as the starting point but diseased cells will be there, then how can be it explained consecutively.
Question: Cellular development RNAseq
27 days ago by
rob.costa1234 • 200
rob.costa1234 • 200 wrote:
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