View source: R/getGnomADvariants.R
getGnomADvariants | R Documentation |
Function retrieves variant data from gnomAD VCF files using tabix for a specified set of genomic regions. It allows users to select the gnomAD version and server location (Google, Amazon, or Microsoft) for fetching the data.
getGnomADvariants(
chr.names,
starts,
ends,
INFO.filter = NULL,
version = "3.1.2",
server = "random"
)
chr.names |
Chromosome names. |
starts |
Start positions. |
ends |
End positions. |
INFO.filter |
Parse only filtered INFO ID. Default is to parse all IDs. |
version |
The gnomAD version. Default to latest version 3.1.2. |
server |
Server locations: "google", "amazon", or "microsoft". Default is random. |
A data.table of VCF.
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