Exomiser 13.1.0 released! Automated ACMG, p-values, simpler output, documentation!

[julesjacobsen]

The three new features for this release is the automated ACMG classification of small sequence variants, calculating
p-values for the combined scores and providing new and more interpretable TSV and VCF output files.

• Added new automated ACMG annotations for top-scoring variants in known disease-causing genes.
• Added new combined score p-value
• Added new TSV_GENE, TSV_VARIANT and VCF output files containing ranked genes/variants for all the assessed modes of
  inheritance. Note that these new file formats will supersede the existing individual MOI-specific TSV/VCF files which
  will be removed in the next major release. See the online documentation for details.
• New update online documentation! See https://exomiser.readthedocs.io/en/latest/
• New Docker hub images for CLI and web on https://hub.docker.com/u/exomiser
• Added checks to ensure user specifies genome assembly if user specifies VCF path outside of phenopacket/analysis
• Added --output-prefix option to enable output prefix directly on the command line
• Updated examples to use the latest recommended settings as per preset derived from 100,000 genomes project

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