And now when it knows that the seqlevels can take two different values.
We can assign a new vector of C values.
Now we have two different chromosomes here.
Often we sought Granges and asserting order seems to be sensible here,
but it's actually relative to the order of a seqlevel.
So here we have seqlevels that are chromosome one and chromosome two,
let's reverse that, so we're essentially saying that chromosome 2 comes before
chromosome 1 and then we're going to solve two main [INAUDIBLE] and
now the seq chromosome 2 is the first range that comes out.
Things with chromosome one and chromosome ten and sort of stand out computer
sorting chromosome ten would happen before chromosome two.
We could also assign a genome to these different things so let's try to do that.
Let's say that the genome of this g range is some string, well let's say hq19.
And it will print it.
We can see it all in 19, and actually turns out if you look at the seek info
slot that every single chromosome can have its own genome.
That seems very esoteric, but that happens because say we seek from saying organisms.
Or say you're spiking in external DNA into our sequencing experiment.
This external DNA sometimes comes as our quality control.
Or spiking controls.
These external pieces of DNA may come from different organisms.