This is a companion discussion topic for the original entry at

PCAWG Broad variant calling workflow is developed by the Broad Institute (](, it consists of software components calling somatic substitutions, indels and structural variations using uniformly aligned tumor / normal WGS sequences. The workflow has been dockerized and packaged using WDL workflow language, the source code is available on GitHub at:

It seems to me that for those who want to use the docker image, you should pull from

The setting of the page seems to be wrong.