View source: R/list_mutations.R
list_mutations | R Documentation |
Quick method to look up mutations of interest prior to using select_cell_lines()
list_mutations(
gene = NULL,
chr = NULL,
start_bp = NULL,
end_bp = NULL,
is_hotspot = NULL,
is_damaging = NULL,
variant_classification = NULL,
data_dir = NULL
)
gene |
string, Hugo Symbol, Default: NULL |
chr |
string, Default: NULL |
start_bp |
integer, Default: NULL |
end_bp |
integer, Default: NULL |
is_hotspot |
logical, TCGA or COSMIC hotspot, Default: NULL |
is_damaging |
logical, Default: NULL |
variant_classification |
string, Default: NULL. Select from the following: For DepMap data version prior to 23Q: 3'UTR, 5'Flank, 5'UTR, De_novo_Start_OutOfFrame, Frame_Shift_Del, Frame_Shift_Ins, IGR, In_Frame_Del, In_Frame_Ins, Intron, Missense_Mutation, Nonsense_Mutation, Nonstop_Mutation, Silent, Splice_Site, Start_Codon_Del, Start_Codon_Ins, Start_Codon_SNP, Stop_Codon_Del, Stop_Codon_Ins For DepMap data version 23Q and after: missense_variant, frameshift_variant, splice_acceptor_variant, stop_gained, splice_donor_variant, inframe_deletion, inframe_insertion, stop_lost, start_lost, downstream_gene_variant, protein_altering_variant, 5_prime_UTR_variant, upstream_gene_variant, non_coding_transcript_exon_variant |
data_dir |
string Path to GRETTA_data |
A data frame containing mutations matching criteria of input arguments
gretta_data_dir <- './GRETTA_example/'
gretta_output_dir <- './GRETTA_example_output/'
if(!dir.exists(gretta_data_dir)){
download_example_data(".")
}
list_mutations(
gene = 'ARID1A',
is_damaging = TRUE,
data_dir = gretta_data_dir)
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