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Hi Will,
quasi-UMIs seem like a great way to feed non-UMI data to UMI-based methods. Thank you for all your work and this R package.
When trying it out with some subset of the Tabula Muris bone marrow smart-seq2 data (count matrix here) the quminorm function finished without any messages or errors, but the resulting matrix had some cells with just 0 and NAs. At first glance, the offending cells are not standing out in the original smart-seq2 count matrix.
Do you have any idea what might be going on? In my particular example there are 130 cells (out of 5,051) giving this problem.
Cheers,
Christoph
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