Read sequence data of multiple genomes (contigs, chromosomes, ...) into a
tidy dataframe and augment it with layout information necessary for plotting.
Usage
as_seqs(x, ...)
# S3 method for tbl_df
as_seqs(x, everything = TRUE, ...)
Value
an tbl_df with plot coordinates
Arguments
x
an object convertible to a sequence layout
...
pass through to layout_seqs()
everything
set to FALSE to drop optional columns
Methods (by class)
as_seqs(tbl_df): Convert a list of tibbles into a seq layout