With recent high-throughput technology we can synthesize large heterogeneous collections of DNA structures, and also read them all out precisely in a single procedure. Can we use these tools, not only to do things faster, but also to devise new techniques and algorithms? In this paper we examine some DNA algorithms that assume high-throughput synthesis and sequencing. We aim to monitor, record, and read out the order in which a number $N$ of events occur, using $N^2$ redundant detectors, and (after sequencing) reconstructing the order by transitive reduction.
翻译:使用最新的高通量技术,我们可以合成大型的多式DNA结构收藏,并且精确地用一个程序读出来。 我们可以使用这些工具,不仅加快工作速度,而且设计新的技术和算法吗? 在这份文件中,我们检查了某些假设高通量合成和排序的DNA算法。 我们的目标是监测、记录和解读事件发生时间的顺序,使用2美元冗余探测器,以及(在排序后)通过中转削减重建秩序。