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Thanks @marcelm for maintaining such a useful tool!
Regarding the relatively new poly-A trimming feature - would it be possible to toggle strandedness?
By default you consider R1 to have the polyA and R2 to have polyT but for applications such as single cell RNA-seq, it can often be the opposite.
The text was updated successfully, but these errors were encountered:
Thanks for the feedback!
As a workaround, you can swap the R1 and R2 input and output files and the read-specific options (such as -a ↔ -A and -m ↔ -M).
-a
-A
-m
-M
This workoraund gets confusing quickly, so I will definitely think about how to make this configurable.
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yep, that's what I've been doing 👍
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Thanks @marcelm for maintaining such a useful tool!
Regarding the relatively new poly-A trimming feature - would it be possible to toggle strandedness?
By default you consider R1 to have the polyA and R2 to have polyT but for applications such as single cell RNA-seq, it can often be the opposite.
The text was updated successfully, but these errors were encountered: