pachterlab / kallisto

Near-optimal RNA-Seq quantification
https://pachterlab.github.io/kallisto
BSD 2-Clause "Simplified" License
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D-list Usage Question #412

Closed yvazirabad closed 1 year ago

yvazirabad commented 1 year ago

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

Yenaled commented 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.

yvazirabad commented 1 year ago

Thank you so much, my intuition was to always turn it on. I appreciate your quick response!

-Ibrahim