21 months ago by
If you are looking to reuse your PacBio reads for scaffolding, that is pretty much a dead end.
If you are asking your question because you do not want to sequence a separate PE library, then you could look to see if there short-read based assemblies and PE libraries for the same species that are publicly available and use those read data to scaffold your contigs. You could get lucky sometimes by just looking :)
If you are strictly looking for non-paired-end based scaffolding, there are orthogonal approaches like BioNano and Hi-C based (super)scaffolding. BioNano is based on optical mapping using restriction sites, and Hi-C is based on spatial organization of chromosomes.