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I have noticed that the between sample normalisation methods in rnanorm automatically remove genes with zero counts across all samples. However would it be possible for this to be optionally, allowing the user to perform custom count filtering prior to passing to rnanorm's TMM normalisation for example.
The text was updated successfully, but these errors were encountered:
There are several pre-filtering approaches that can be used in RNAseq count data analysis:
filterByExpr
in the edgeR R package (https://f1000research.com/articles/5-1438)I have noticed that the between sample normalisation methods in rnanorm automatically remove genes with zero counts across all samples. However would it be possible for this to be optionally, allowing the user to perform custom count filtering prior to passing to rnanorm's TMM normalisation for example.
The text was updated successfully, but these errors were encountered: