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susannasiebert committed Apr 23, 2018
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2 changes: 1 addition & 1 deletion docs/conf.py
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# The short X.Y version.
version = '1.0'
# The full version, including alpha/beta/rc tags.
release = '1.0.3'
release = '1.0.4'

# The language for content autogenerated by Sphinx. Refer to documentation
# for a list of supported languages.
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16 changes: 5 additions & 11 deletions docs/index.rst
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This is a hotfix release. It fixes the following issues:

- Stop-gain mutation were previously not handled correctly. If a mutation had
a \* (stop gain) in the VEP Amino_acids field, pVACseq would throw an error.
We now ensure that those cases are handled. pVACseq will also skip stop-gain
mutations if the resulting mutant peptide sequence is not novel.
- pVACseq would previously throw an error if multiple mutations resulted
in the same consequence. This is now handled by assigning a unique
identifier to each mutation.
- We added a better warning messages if the chosen prediction algorithms and
alleles MHC classes are mutually exclusive, e.g., if only class I prediction
algorithms were chosen with only class II alleles. Previously, pVACseq would
simply finish without producing any output or errors.
- We discovered a couple more cases of mutations involving stop codons that
would result in errors. These are amino acid changes (VEP Amino_acids field)
for large indels that would span exon boundaries (multiple \* in the Amino_acids
field), or amino acid changes involving the transcript stop codon (ending in X).
These cases are now handled.

Coming soon
-----------
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2 changes: 1 addition & 1 deletion setup.py
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setup(
name="pvactools",
version="1.0.3",
version="1.0.4",
packages=["tools", "tools.pvacfuse", "tools.pvacvector", "tools.pvacseq", "lib", "utils.pvacapi", "utils.pvacapi.controllers"],
entry_points={
"console_scripts":[
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