dot-infer_variant_type: Infer variant type if not present in data
In MSKCC-Epi-Bio/gnomeR: Wrangle and analyze IMPACT and TCGA mutation data
.infer_variant_type R Documentation
Infer variant type if not present in data
Description
Infers variant_type from reference_allele or tumor_seq_allele data
Usage
.infer_variant_type(mutation, names_mut_dict = names_mut_dict)
Arguments
mutation
mutation maf file data frame
Value
a mutation data frame with a variant type column
MSKCC-Epi-Bio/gnomeR documentation built on Oct. 17, 2024, 3:39 p.m.
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| .infer_variant_type | R Documentation |
Infer variant type if not present in data
Description
Infers variant_type from reference_allele or tumor_seq_allele data
Usage
.infer_variant_type(mutation, names_mut_dict = names_mut_dict)
Arguments
mutation |
mutation maf file data frame |
Value
a mutation data frame with a variant type column
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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