@@ -186,7 +186,7 @@ for and as well as details on the transcripts itself.
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The Peptide Candidates from Selected Transcript Set tab shows a list of
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mutant and matched wildtype peptides and their IC50 binding
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affinity to the patient HLA alleles. Only neoantigen candidate were at least
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- opne peptide-MHC binding prediction falls within the ` --aggregate-inclusion-threshold `
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+ one peptide-MHC binding prediction falls within the ` --aggregate-inclusion-threshold `
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will be shown in this table. For HLA alleles were the peptide is not
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well-binding the prediction details will show ` X ` . This table also shows the
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mutant position, whether or not the neoantigen candidate has any problematic
@@ -217,7 +217,7 @@ panel.
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The first tab, "IC50 Plot", shows violin plots of the predicted IC50 binding
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affinity for each prediction algorithm for both the neoantigen candidate and
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its matched wildtype peptide. This can be used to check concordance
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- of predicitions between the different algorithms. It also allows for a
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+ of predictions between the different algorithms. It also allows for a
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detailed comparison between the mutant and wildtype predictions in addition to
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the median or lowest IC50 binding affinity used elsewhere. A solid line is used
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to represent the median score.
@@ -259,6 +259,12 @@ panel.
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ottrpal::include_slide("https://docs.google.com/presentation/d/1uz39zaObDGKhEVCGzO0JO35CTbC0oRAM0mxgLcMAA9Y/edit#slide=id.g25ad9ce8c9b_0_68")
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```
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+ ## Regenerate Tiers with Custom Parameters
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+
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+ ## Adding Comments to Variants
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+
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+ ## Exporting the Aggregated Table
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+
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## Tour of the pVACview interface
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Here is a brief tour of the [ pVACview] ( https://pvactools.readthedocs.io/en/latest/pvacview.html ) {target="_ blank"} interface:
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