This service allows the user to query information about variants on a certain chromosome at a certain location.
Arguments
- start
Integer.
- end
Integer.
- chromosome
String. One of "chr1", "chr2", "chr3", "chr4", "chr5", "chr6", "chr7", "chr8", "chr9", "chr10", "chr11", "chr12", "chr13", "chr14", "chr15", "chr16", "chr17", "chr18", "chr19", "chr20", "chr21", "chr22", "chrM", "chrX", "chrY".
- sortBy
String. Options: "sampleId", "ischemicTime", "aliquotId", "tissueSampleId", "hardyScale", "pathologyNotes", "ageBracket", "tissueSiteDetailId", "sex".
- sortDirection
String. Options: "asc", "desc". Default = "asc".
- datasetId
String. Unique identifier of a dataset. Usually includes a data source and data release. Options: "gtex_v8", "gtex_snrnaseq_pilot".
- page
Integer (default = 0).
- itemsPerPage
Integer (default = 250). Set globally to maximum value 100000 with
options(list(gtexr.itemsPerPage = 100000)).- .verbose
Logical. If
TRUE(default), print paging information. Set toFALSEglobally withoptions(list(gtexr.verbose = FALSE)).- .return_raw
Logical. If
TRUE, return the raw API JSON response. Default =FALSE
See also
Other Datasets Endpoints:
get_annotation(),
get_collapsed_gene_model_exon(),
get_downloads_page_data(),
get_file_list(),
get_full_get_collapsed_gene_model_exon(),
get_functional_annotation(),
get_linkage_disequilibrium_by_variant_data(),
get_linkage_disequilibrium_data(),
get_sample_datasets(),
get_subject(),
get_tissue_site_detail(),
get_variant()
