Check out overlaps between different genomic positions on same chromosome and set up layer numbers for each line of the genomic data.
A data frame with genomic positions (chromosomes, start and end positions) and the positions should be already validated and sorted by chromosome then start position.
Non-negative integer, total number of columns for genomic positions.
A non-negative integer vector with length same as the total rows of input data.
library(RCircos) data(RCircos.Tile.Data) layers <- RCircos.Get.Plot.Layers(RCircos.Tile.Data, 3)
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