DeepSomatic (https://t.co/BqZkDNMv1E) preprint is out showing improvements in somatic variant calling in various platforms.
Work lead by @jiimiinpaark and @daniel_e_cook. Tumor-only lead by @pichuan. In collaboration with @acarroll_ATG, @MishaKolmogorov and @BenedictPaten. 🧵1/7
@d0m96 https://t.co/MAGfNOJ5EP works well. Supports more complex operations (log, exp, etc) if you prefix your calculation with ‘=‘. Has a history and clipboard support.
@aarondfrancis There are two sets of twins in my family. One identical and one fraternal. It’s fun because I can say I have 3 twin brothers. Good luck!
This @rustlang tool is part of my work @GoogleHealth’s genomics team (hosts: @daniel_e_cook and @belyaeva_ana). We use it for evaluating DeepConsensus, though it should be generally useful for evaluating basecalling or other sequencing methods
Github: https://t.co/AhUvrBYw5v
@brent_p@brent_p This is the approach I take generally. I tried to create a general purpose environment but too many dependencies clashed. This works well in the context of Nextflow, and I also use conda within Docker for convenience.