python mutation_report.py --string EDLTVKIGDFGLATEKSRWSGSHQFEQLS --hla "HLA-B*35:01"
python mutation_report.py --input-file <.vcf, .maf, .tab, .fasta> --hla-file <allele-file>
If VCF file is input, it will be annotated w/ gene information and Ensembl transcripts, otherwise input an annotated SnpEFF VCF file.
If you don't either an hla
or hla-file
then the default "HLA:A*02:01" will be used.
--input-file
: Input file containing somatic variants (one of MAF, VCF, or SnpEff annotated VCF)--string
: String of amino acids, with optional annotation of a mutated region between underscores (i.e. QYS_LL_Q)--hla
: Comma separated list of HLA alleles. --hla-file
: Text file containing one HLA allele per line. --peptide-length
: Length of vaccine peptide (window around mutation, default 31)--min-peptide-padding
: Minimum number of wildtype residues before or after a mutation --print-epitopes
: Print dataframe with epitope scores--print-peptides
: Print dataframe with vaccine peptide scores--output-epitopes-file
: CSV output file for dataframe containing scored epitopes--output-report-file
: Path to HTML report containing scored vaccine peptides and epitopes--random-mhc
: Random values instead for MHC binding prediction--iedb-mhc
: Use IEDB's web API for MHC binding--skip-mhc
: Don't predict MHC binding--quiet
: Suppress verbose outputYou must either have netMHCpan installed locally or pass the iedb-mhc
flag to use a web-based MHC binding predictor.