Design automation for deterministic lateral displacement by leveraging deep Q-network.

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS
Biomicrofluidics Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI:10.1063/5.0243605
Yuwei Chen, Yidan Zhang, Junchao Wang
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引用次数: 0

Abstract

Despite the widespread application of microfluidic chips in research fields, such as cell biology, molecular biology, chemistry, and life sciences, the process of designing new chips for specific applications remains complex and time-consuming, often relying on experts. To accelerate the development of high-performance and high-throughput microfluidic chips, this paper proposes an automated Deterministic Lateral Displacement (DLD) chip design algorithm based on reinforcement learning. The design algorithm proposed in this paper treats the throughput and sorting efficiency of DLD chips as key optimization objectives, achieving multi-objective optimization. The algorithm integrates existing research results from our team, enabling rapid evaluation and scoring of DLD chip design parameters. Using this comprehensive performance evaluation system and deep Q-network technology, our algorithm can balance optimal separation efficiency and high throughput in the automated design process of DLD chips. Additionally, the quick execution capability of this algorithm effectively guides engineers in developing high-performance and high-throughput chips during the design phase.

利用深度q -网络设计确定性横向位移的自动化。
尽管微流控芯片在细胞生物学、分子生物学、化学和生命科学等研究领域得到了广泛的应用,但为特定应用设计新芯片的过程仍然复杂且耗时,往往依赖于专家。为了加速高性能、高通量微流控芯片的发展,本文提出了一种基于强化学习的自动化确定性横向位移(DLD)芯片设计算法。本文提出的设计算法以DLD芯片的吞吐量和分选效率为关键优化目标,实现了多目标优化。该算法集成了我们团队现有的研究成果,能够快速评估和评分DLD芯片设计参数。利用该综合性能评价体系和深度q -网络技术,我们的算法可以在DLD芯片的自动化设计过程中平衡最佳分离效率和高吞吐量。此外,该算法的快速执行能力有效地指导工程师在设计阶段开发高性能和高吞吐量的芯片。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomicrofluidics
Biomicrofluidics 生物-纳米科技
CiteScore
5.80
自引率
3.10%
发文量
68
审稿时长
1.3 months
期刊介绍: Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications. BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics. Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary) Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification) Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation) Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles) Cell culture and analysis(single cell assays, stimuli response, stem cell transfection) Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays) Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers) Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...
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