Description Usage Arguments Examples
Function to load vcf file for a particular genomic region
1 2 | loadVcfFileForRegion(vcfFile, chr, start, end, includeFilteredSites = F,
n = -1, refVersion = "GRCh37", returnGenotypes = F)
|
vcfFile |
File name to load |
chr |
Chromosome/contig to load |
start |
Initial genomic position to load |
end |
Final genomic position to load |
includeFilteredSites |
Return filtered-out sites (i.e. sites marked with anything other than PASS on vcf). Defaults to FALSE |
n |
Max number of records to load. Set to -1 for no limit. |
refVersion |
Reference version. Defaults to "GRCh37". |
returnGenotypes |
Return genotype data. Default to FALSE. |
1 | exacdata<- loadVcfFileForRegion('exac.vcf',"1",12345600,13345600)
|
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