Always love seeing more educational content on a topic that helped launch my academic career!
How do you spot amplified cancer genes in noisy sequencing data? Find out in my latest interactive article with @etalevich.bsky.social, where you get to run CNVkit (Python) and DNAcopy (R) in your browser on real data to see how CNV calling works under the hood. ➡️ sandbox.bio/concepts/cnv