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Fix spelling errors
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03-running_pvactools.Rmd

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pVACseq is used to identify neoantigens from missense, inframe indel, and
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frameshift mutations. The pipeline uses a somatic VCF file as an input, which
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represents variants called in the tumor sample. The VEP annoations in the VCF file
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represents variants called in the tumor sample. The VEP annotations in the VCF file
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inform the variant type of a variant and their consequence on the gene transcripts
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overlapping the genomic coodinates of the variant. The amino acid change of
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overlapping the genomic coordinates of the variant. The amino acid change of
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the predicted consequence if used by pVACseq to calculate the mutated peptide sequence.
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The pVACseq pipeline is run using the `pvacseq run` command.
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## Running pVACfuse
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pVACfuse is run to in order to predict neoantigens from fusion events. The
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pipeline uses annotated fusion calls from eithe AGFusion or Arriba for this
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pipeline uses annotated fusion calls from either AGFusion or Arriba for this
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purpose. These annotators already include the fusion peptide sequence in their
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outputs which pVACfuse uses to extract neoantigens around the fusion position.
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resources/dictionary.txt

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DataTrail
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Dockerfile
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Dockerhub
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deprioritized
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dropdown
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epitope
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epitopes
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HLA
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histocompatibility
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https
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http
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IC
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IEDB
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ITCR
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isoform
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immunogenomics
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impactful
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indel
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indels
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inframe
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itcrtraining

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