John Simpson

TL;DR: A scalable, highly parallel sequencing system with raw throughput significantly greater than that of state-of-the-art capillary electrophoresis instruments with 96% coverage at 99.96% accuracy in one run of the machine is described.

TL;DR: In this article, methods and apparatuses for sequencing a nucleic acid are presented. But their methods require a large number of independent sequencing reactions to be arrayed in parallel, permitting simultaneous sequencing of a very large number (>10,000) of different oligonucleotides.

TL;DR: In this article, the authors proposed methods by which biologically derived DNA sequences in a mixed sample or in an arrayed single sequence clone can be determined and classified without sequencing, making use of information on the presence of carefully chosen target subsequences, typically of length from 4 to 8 base pairs.

TL;DR: In this article, methods and apparatuses for sequencing a nucleic acid are presented. But their methods require a large number of independent sequencing reactions to be arrayed in parallel, permitting simultaneous sequencing of a very large number (>10,000) of different oligonucleotides.

TL;DR: In this paper, a device for separating charged particles comprising an upper substate (11), a lower substrate (12), separation lanes (15) defined on the upper substrate, a first plurality of electrodes (21, 22, 23), a first pad (18), a second pad (19, 20, 21, 22), a third pad (23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46,