get_studies | R Documentation |
Retrieves studies via the NHGRI-EBI GWAS Catalog REST API. The REST
API is queried multiple times with the criteria passed as arguments (see
below). By default all studies that match the criteria supplied in the
arguments are retrieved: this corresponds to the default option
set_operation
set to 'union'
. If you rather have only the
studies that match simultaneously all criteria provided, then set
set_operation
to 'intersection'
.
get_studies(
study_id = NULL,
association_id = NULL,
variant_id = NULL,
efo_id = NULL,
pubmed_id = NULL,
user_requested = NULL,
full_pvalue_set = NULL,
efo_uri = NULL,
efo_trait = NULL,
reported_trait = NULL,
set_operation = "union",
interactive = TRUE,
verbose = FALSE,
warnings = TRUE
)
study_id |
A character vector of GWAS Catalog study accession identifiers. |
association_id |
A character vector of GWAS Catalog association identifiers. |
variant_id |
A character vector of GWAS Catalog variant identifiers. |
efo_id |
A character vector of EFO identifiers. |
pubmed_id |
An integer vector of PubMed identifiers. |
user_requested |
A |
full_pvalue_set |
A |
efo_uri |
A character vector of EFO URIs. |
efo_trait |
A character vector of
EFO trait descriptions, e.g.,
|
reported_trait |
A character vector of phenotypic traits as reported by the original authors of the study. |
set_operation |
Either |
interactive |
A logical. If all studies are requested, whether to ask interactively if we really want to proceed. |
verbose |
Whether the function should be verbose about the different queries or not. |
warnings |
Whether to print warnings. |
Please note that all search criteria are vectorised, thus allowing for batch
mode search, e.g., one can search by multiple variant identifiers at once by
passing a vector of identifiers to variant_id
.
A studies object.
## Not run:
# Get a study by its accession identifier
get_studies(study_id = 'GCST001085', warnings = FALSE)
# Get a study by association identifier
get_studies(association_id = '25389945', warnings = FALSE)
# Get studies by variant identifier
get_studies(variant_id = 'rs3798440', warnings = FALSE)
# Get studies by EFO trait identifier
get_studies(efo_id = 'EFO_0005537', warnings = FALSE)
## End(Not run)
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