Are there any new technologies which can be used in the future to identify INDELs, translocation, etc?

As far as I know, previous software/methods mainly applied paired-end reads (soft clipped reads and discordant reads) to capture this type of variants.

Currently, long read sequences such as Nanopore and Pacbio might be used to more accurately identify structure variants.

I am opening this topic and look for more discussion and ideas.