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