The GenomicVis package contains a collection of function for the
visualisation of genomic data typically derived from high-throughput
whole genome sequencing and SNP-Chip experiments. Most of the functions
provided by this package are agnostic about where the data actually comes
from, that is, they required input in simple data.frame
instances
that are not tied to a particular file format; however, we also provide
many examples of creating these simply data.frame
s from standard
file formats such as VCFs and from common software tools such as GAP and
Breakdancer.
For further details, and examples, users are directed to the package
vignette: run vignette('GenomicVis')
from the R prompt.
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