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All functions

annotate_coding()
Annotate VCF variants with coding changes
annotate_fusions()
Aggregate fusion VCFs into a table
count_fastq()
Count barcodes directly from source FASTQ files
filter_fusions()
Filter a fusion VRanges object by number of reads and tools
filter_variants()
Make results report to save as xlsx sheets (full, filtered, peptides)
make_peptides()
Make a variants report as named list of tables
make_report()
Make a variants report as named list of tables
pep_tile()
Tile cDNA into peptide sequences
pepitope-package pepitope
Pepitope: peptide epitopes from reference genome and variant (VCF) file
plot_barcode_overlap()
Plot barcode overlap between different samples
plot_read_count() plot_reads()
Plot the overall read counts
plot_read_distr() plot_distr()
Plot the read distribution across barcodes
plot_read_structure()
Plot annotated read structure examples
plot_screen()
Plot screen results
remove_cutsite()
Remove a Restriction Enzyme cut site but keep AA in a tiled peptide data.frame
screen_calc()
Calculate differential abundance of construct barcodes
subset_context()
Subset nucleotide/protein sequences to codon +/- 45 bp context
subset_context_fusion()
Subset the peptide context for gene fusions