新议题2B:为什么(重新)设计生物学比设计电子学更具有挑战性

B. Kaminska, B. Courtois, S. Hassoun
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摘要

考虑现有复杂SoC的重新旋转,具有部分原理图和不完整的规范,具有有限的测试和观察I/O行为的能力。此外,所使用的底层技术也只是部分地被理解。有纪律的工程方法能产生重新旋转吗?根本性的挑战是什么?自动化工具将如何实现这样的设计?本讲座将展示分析和合成概念如何在生物发现和设计的背景下应用。各种优化和分析技术可以应用于在不杀死大肠杆菌细胞的情况下最大限度地生产乙醇。途径合成技术可以帮助揭示人类肠道内环境化学物质的命运,肠道由属于~ 1000种的~ 1014种细菌定植。参加这个讲座不需要生物学的先决条件。
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New topic session 2B: Why (Re-)Designing Biology is ∗Slightly∗ more challenging than designing electronics
Consider a re-spin of an existing complex SoC, with a partial schematic and an incomplete specification, with limited abilities to test and observe I/O behavior. Additionally, the underlying technology used is only partially understood. Can disciplined engineering approaches yield the re-spin? What are fundamental challenges? How will automation tools enable such designs? This talk will showcase how analysis and synthesis concepts can be applied in the context of biological discovery and design. Various optimization and analysis techniques can be applied to maximize the production of ethanol within an E. Coli cell without kill it. Pathway synthesis techniques can help uncover the fate of environmental chemicals within the human gut, which is colonized by ∼1014 bacteria belonging to ∼1000 species. No biology pre-requisites are needed to attend this talk.
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