Retrieve Fine Mapping Data
Finds and returns
Fine Mapping
data for the provided list of genesBy default, this endpoint fetches data from the latest
GTEx
version
The retrieved data is split into pages with items_per_page
entries per page
Usage
get_fine_mapping(
gencodeIds,
datasetId = "gtex_v8",
variantId = NULL,
tissueSiteDetailIds = NULL,
page = 0,
itemsPerPage = 250
)
Arguments
- gencodeIds
A character vector of Versioned GENCODE IDs, e.g. c("ENSG00000132693.12", "ENSG00000203782.5").
- datasetId
String. Unique identifier of a dataset. Usually includes a data source and data release. Options: "gtex_v8", "gtex_snrnaseq_pilot".
- variantId
String. A gtex variant ID.
- tissueSiteDetailIds
Character vector of IDs for tissues of interest. Can be GTEx specific IDs (e.g. "Whole_Blood"; use
get_tissue_site_detail()
to see valid values) or Ontology IDs.- page
Integer (default = 0).
- itemsPerPage
Integer (default = 250).
See also
Other Static Association Endpoints:
get_eqtl_genes()
,
get_independent_eqtl()
,
get_multi_tissue_eqtls()
,
get_significant_single_tissue_eqtls()
,
get_significant_single_tissue_eqtls_by_location()
,
get_significant_single_tissue_ieqtls()
,
get_significant_single_tissue_isqtls()
,
get_significant_single_tissue_sqtls()
,
get_sqtl_genes()
Examples
if (FALSE) { # \dontrun{
# search by gene
get_fine_mapping(gencodeIds = c("ENSG00000132693.12",
"ENSG00000203782.5"))
# optionally filter for a single variant and/or one or more tissues
get_fine_mapping(gencodeIds = c("ENSG00000132693.12",
"ENSG00000203782.5"),
variantId = "chr1_153228363_A_G_b38",
tissueSiteDetailIds = c("Whole_Blood",
"Thyroid"))
} # }