Entering edit mode
7.4 years ago
ly.leifels
•
0
How can I deal with overdispersion in single-cell RNA seq experiments? especially regarding low counts?
How can I deal with overdispersion in single-cell RNA seq experiments? especially regarding low counts?
What have you tried so far? One sensible solution might be to try:
If those don't get you to where you need to be, then where's the gap? Do you think the estimates are off, and if so, why? Or maybe you just need more reliable quantification of uncertainty?
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For clustering, or differential expression, or something else entirely?
for clustering genes into gene modules