I see, so if you sequenced the DNA going towards a telomere at one end, and away from the telomere at the other, those sequences are on the same strand even though you have the 'gap' of the unsequenced centromere in the middle. Same would be true for DNA going towards/away from the centromere.
I guess this is only a problem when you don't have a genetic landmark and your DNA is just a small fragment. But the strandedness also determines the orientation and thus order of the genes, so you could use FISH or whatever you to see if Gene A before the gap is closer to Gene B (at one end of the fragment) or Gene C (other end of the fragment).
Man.... i don't envy people doing de novo assembly one bit :P Thanks guys!
In general I think that it is safe to assume that there are checks and balances in place to ensure that sequences separated by gaps are on the same strand.
Without understanding how it could be theoretically possible, I would avoid assuming anything :P
I think one issue here is that "sense strand" and "antisense strand" are confusing terms and not especially helpful.
indeed, this is a terminology that I also find to be both unfortunate and inappropriate. Same with calling them "top" and "bottom" strands.