In single-cell RNA-seq, every droplet is contaminated. 5–20% of the counts aren't from the cell you think.
Ignore ambient RNA and you'll call doublets "rare hybrid cell types."
Do you need an intro to analyzing (prote)omics data?
This series of lectures may be helpful.
We aimed to make them short & accessible.
Enjoy watching & learning !
https://t.co/gTHe1J19Jq
I translated IdeaScientist's research workflow into a native Claude Code plugin.
Give it a problem. Agents search literature, find gaps, propose an idea, challenge it, and draft a falsifiable proposal.
4 skills. 7 agents. One command.
https://t.co/zGQFzjVGwL
Your RNA-seq targets mature mRNA, right? So why are so many reads landing in introns?
What intronic reads actually mean — and when they're signal, not noise.