available_studies()
that arose with underlying API change from V2 to V3.lookup_id()
function to return all samples that exist across cBioPortal for a given patient ID.available_sample_lists()
function which returns all available sample list IDs for a given study IDsample_list_id
argument to available_samples()
which returns all samples IDs in specific sample list within a study (#53).get_segments_by_sample()
and get_segments_by_study()
). You can use get_genomics_by_*(return_segments = TRUE)
as well to access this data.This version makes the package compatible with cBioPortal v5.0. Main updates include:
structural-variant
instead of fusion
in specification.get_structural_variants_by_sample()
and get_structural_variants_by_study()
added as aliases for get_fusions_by_sample()
and get_fusions_by_study()
. These functions return the same results as their fusion counterparts and both names will be supported.data_type
argument, structural_variant
is now available as option. This will return the same results as fusion
.get_genetics_by_sample()
and get_genetics_by_study()
functions are now named lists with names: mutation
, cna
, and structural_variant
(changed from fusion
) to be consistent with cBioPortal v5.0 naming conventions.prad_msk_2019_structural_variants
-> prad_msk_2019_structural_variants
)add_hugo
argument of get_*_by_sample()
functions.This is the first release submitted to CRAN, and includes all updates (listed below under versions 0.2.0 and 0.2.1) made since last Github release (0.1.0). Package has been overhauled since first release (0.1.0), and code will not be backwards compatible with that version.
get_genomics_by_sample()
and related functions to pull all gene data available for select samples instead of pulling data for IMPACT genes only by defaultget_genomics_by_sample()
and related functions.get_genomics_by_sample()
and related functions to pull all gene data available for selected sample by default instead of
pulling data for IMPACT genes only by default. This will change default results when user does not specify genes, and could return more results than previously as they will include results for non IMPACT gene mutations, CNA or fusions, if available.get_genomics_by_sample()
and related functions (previously had to specify by Entrez Gene ID or NULL
) (#33)get_genomics_by_sample()
and related functions with new panel
argument. Previously could only specify genes
by specified sets of gene IDs. (#15)sample_id
, study_id
), but now accept any capitalization/delimiters (e.g. sampleID
, sample id
) (#16)cbp_api()
.get_data_by_study()
and .get_data_by_sample()
with wrappers for each data type