Open mjsduncan opened 2 years ago
Hi @mjsduncan ! our documentation is here: https://bcbio-nextgen.readthedocs.io/en/latest/index.html Unfortunately, we are not doing joint DNA+RNA analysis. You could run a DNA variant calling and RNA-seq alignment/abundance separately. SN
i'm a newbie to sequencing analysis & working on a pooled sample project for the first time. i've found this slide deck from Yeaman lab to be helpful, but expert curated examples of pooled sample DNA variant calling and RNAseq abundance & other pipelines in one place would be very useful.
thanks to all for continuing to develop and maintain this project.