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Hi, I've tried to run "run_deseq2" from microbiomeMarker package and "DESeq" form DESeq2 package with the same data set and with defaults parameters with both packages. I expected to have the same results or at least very similar instead they are completely different. I am working with microbiome data (with many zeros) and now I am wondering which of the two package I should believe. Are the default settings of "run_deseq2" optimized for microbiome data? If so, which are those settings?
Kind regards
The text was updated successfully, but these errors were encountered:
First, filtering taxa whose abundance is zero in your OTU table, and then run Deseq() with sfType = "poscounts" , you can get the same result with run_deseq2().
Hi, I've tried to run "run_deseq2" from microbiomeMarker package and "DESeq" form DESeq2 package with the same data set and with defaults parameters with both packages. I expected to have the same results or at least very similar instead they are completely different. I am working with microbiome data (with many zeros) and now I am wondering which of the two package I should believe. Are the default settings of "run_deseq2" optimized for microbiome data? If so, which are those settings?
Kind regards
The text was updated successfully, but these errors were encountered: