My lab has paired bulk and single cell RNAseq for several tumor samples. We'd like to somehow use our single cell results (basically annotated clusters of cells w/ cell identities and differentially expressed genes, plus a malignant / normal cell label) to inform our bulk RNAseq analysis, but I'm somewhat lost on where to begin. I've been looking for papers on joining the data from the two technologies but I haven't found anything super useful yet. Any ideas / hints on where to start, or what papers I should be reading would be excellent.
forgot to mention he has some good videos on youtube that could serve as an introduction
Is this the presentation to which you are referring? I can't find any UW videos with Dr. Shalek that are recent.