Closed yvazirabad closed 1 year ago
I would always turn it on.
It's not a question of bulk vs. single-cell; it's a question of "what's in your sequencing reads" (which, unfortunately, no one ever really knows).
So yeah, I would always turn it on (whether bulk or single-cell or something else) -- you never know how much of your sequencing reads is contaminated with genomic DNA or whether unspliced molecules were abundantly captured by the library prep.
Thank you so much, my intuition was to always turn it on. I appreciate your quick response!
-Ibrahim
Hello,
This is more of a usage guideline ask rather than any issue in Kallisto. Since the advent of the d-list option in Kallisto, I have been wondering if it should always be turned on when running either bulk or single-cell RNA-Seq, or if the d-list finds the most utility with scRNA-Seq and using it for bulk RNA-Seq is not very helpful.
-Ibrahim Vazirabad