closest_germline | R Documentation |
Uses gnomAD to annotate the nearest germline event to each structural variant. For more information read gnomAD blog. Reference is in hg38.
closest_germline(bp = NULL, cores = 1, genome = NULL)
bp |
Bedpe from svaba_vcf2bedpe or manta_vcf2bedpe |
cores |
Number of cores to run on, default is 1 |
genome |
run under hg19 or hg38 |
Bedpe with a column added for distance to nearest germline event
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