get_genetics_by_sample {cbioportalR}

Get All Genomic Information By Sample IDs

Description

Get All Genomic Information By Sample IDs

Usage

get_genetics_by_sample(
  sample_id = NULL,
  study_id = NULL,
  sample_study_pairs = NULL,
  genes = NULL,
  panel = NULL,
  add_hugo = TRUE,
  base_url = NULL,
  return_segments = FALSE
)

Arguments

sample_id

a vector of sample IDs (character)

study_id

A string indicating the study ID from which to pull data. If no study ID, will guess the study ID based on your URL and inform. Only 1 study ID can be passed. If mutations/cna from more than 1 study needed, see sample_study_pairs

sample_study_pairs

A dataframe with columns: sample_id, study_id and molecular_profile_id (optional). Variations in capitalization of column names are accepted. This can be used in place of sample_id, study_id, molecular_profile_id arguments above if you need to pull samples from several different studies at once. If passed this will take overwrite sample_id, study_id, molecular_profile_id if also passed.

genes

A vector of Entrez ids or Hugo symbols. If Hugo symbols are supplied, they will be converted to entrez ids using the get_entrez_id() function. If panel and genes are both supplied, genes from both arguments will be returned. If both are NULL (default), it will return gene results for all available genomic data for that sample.

panel

One or more panel IDs to query (e.g. 'IMPACT468'). If panel and genes are both supplied, genes from both arguments will be returned. If both are NULL (default), it will return gene results for all available genomic data for that sample.

add_hugo

Logical indicating whether HugoGeneSymbol should be added to your resulting data frame, if not already present in raw API results. Argument is TRUE by default. If FALSE, results will be returned as is (i.e. any existing Hugo Symbol columns in raw results will not be removed).

base_url

The database URL to query If NULL will default to URL set with ⁠set_cbioportal_db(<your_db>)⁠

return_segments

Default is FALSE where copy number segmentation data won't be returned in addition to the mutation, cna and structural variant data. TRUE will return any available segmentation data with results.

Value

A list of mutations, cna and structural variants (including fusions), if available. Will also return copy number segmentation data if return_segments = TRUE.

Examples

## Not run: 
get_genetics_by_sample(sample_id = c("TCGA-OR-A5J2-01","TCGA-OR-A5J6-01"),
 study_id = "acc_tcga",
 return_segments = TRUE)

## End(Not run)