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 class 'tbl_df'
as_seqs(x, everything = TRUE, ...)
Arguments
- x
an object convertible to a sequence layout
- ...
pass through to layout_seqs()
- everything
set to FALSE to drop optional columns
Value
an tbl_df with plot coordinates
Details
Obligatory columns are seq_id
, bin_id
and length
.
Examples
chr <- tibble::tibble(
seq_id = c("a1", "b1", "b2"),
bin_id = c(rep("A", 1), rep("B", 2)),
length = c(5000, 3000, 1400)
)
as_seqs(chr)