Version 5.0

Version 5.0.0

This version adds the following features, outlined below. Please note that pVACtools 5.0 is not guaranteed to be backwards-compatible and certain changes could break old workflows.

New Tools

This release adds a new tool, pVACsplice, for prediction neoantigens from splice sites. Please see the full tool documentation for more information. by @mrichters in https://github.com/griffithlab/pVACtools/pull/911

New Features

  • This release refactors the pVACvector graph building algorithm in order to increase the probability for finding a solution and reduce the number of iterations needed before a solution is found. Please see the PR describtion for the full details. by @susannasiebert in https://github.com/griffithlab/pVACtools/pull/1163

  • Add a new --aggregate-inclusion-count-limit parameter to set the maximum number of epitopes to include in the metrics.json detailed data for variants that have a large number of candidate neoantigens (e.g., frameshifts). by @susannasiebert in https://github.com/griffithlab/pVACtools/pull/1147

  • Add a new --biotypes parameter which defines a list of transcript consequence biotypes that the predictions from pVACseq and pVACsplice should be limited to. by @mrichters in https://github.com/griffithlab/pVACtools/pull/911

  • Add support for additional alleles that weren’t previously supported, includings ones for dog, mouse, and MHC class II. by @susannasiebert in https://github.com/griffithlab/pVACtools/pull/1148

Bugfixes

Version 5.0.1

This is a bugfix release. It fixes the following problem(s):