Man pages for Bio-Core/BioCore.Annotation
BioCore Variant Annotation Package

add_protein_change_columnAdd protein change column.
add_read_depth_columnAdd a read depth column to the ANNOVAR output dataframe.
add_sample_nameAdd sample namel
add_snvidAdd SNVID
add_variant_allele_fraction_columnAdd variant allele fraction (VAF) column to dataframe.
create_merged_dataCreate merged data
create_recurrence_heatmapCreate recurrence heatmap
create_recurrence_tableCreate a table of recurrently mutated genes.
create_variant_signature_barplotCreate the variant signature barplot
filter_annovar_dataFilter ANNOVAR data
filter_on_depthFilter on depth.
filter_on_populationFilter on population data.
get_annovar_colnamesGet the ANNOVAR column names
get_annovar_filesGet a list of ANNOVAR files.
get_coding_mutationsGet coding mutations.
get_pyrimidine_changeGet pyrimidine change
get_read_depthGet the read depth.
get_snvGet single nucleotide variants (SNVs)
get_variant_allele_fractionGet the variant allele fraction from the FORMAT string.
load_annovar_fileLoad an ANNOVAR file.
Bio-Core/BioCore.Annotation documentation built on Feb. 3, 2020, 6:01 p.m.