sv-callers
Highly portable parallel workflow to detect structural variants in cancer genomes.
Highly portable parallel workflow to generate artificial genomes with structural variants.
This Snakemake-based workflow generates artificial short-read alignments based on a reference genome with(out) SVs. The workflow is easy to use and deploy on any Linux-based machine. In particular, the workflow supports automated software deployment, easy configuration and addition of new analysis tools as well as enables to scale from a single computer to different HPC clusters with minimal effort.
Identification and prioritization of cancer-causing structural variations in whole genomes
Highly portable parallel workflow to detect structural variants in cancer genomes.
A command line interface for the Xenon library that allows you to use remote machines to do your computations.
Python library for YAML type inference, schema checking and syntactic sugar.