“…As another family of nanopores, biological pores naturally 1–4 nm in diameter, such as α-hemolysin (α-HL), Mycobacterium smegmatis protein A, Phi29 connector, Aerolysin, Cytolysin A, Outer Membrane Protein G, etc., have been explored for biosensing applications especially in DNA sequencing. In order to improve the sensing performance, efforts have been pursued with respect to novel device structures, such as field-effect transistor (FET)-nanopore devices, , pore-cavity–pore device, and zero-depth nanopore, and to new detection methods, such as plasmonic nanopore and scattering nanopore, as well as to unconventional signal pick-up circuits and data processing algorithms. − These attempts have an implicit focus on boosting the capability of single nanopores in sensing. In contrast, simultaneous translocation of a multitude of nanopores or nanochannels by a large number of nanoparticles for high-throughput and low-cost parallelized sensing has received much less attention.…”