2023
DOI: 10.1109/jeds.2023.3293234
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Active-Matrix Digital Microfluidics Design and Optimization for High-Throughput Droplets Manipulation

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Cited by 5 publications
(2 citation statements)
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“…However, with the development of the digital microfluidic technology, the number of electrodes has been further increased to achieve higher parallel processing capabilities. In our previous work, the number of electrodes in a chip was 4096, with a single droplet volume of 10 nL. , Existing temperature control methods cannot meet the requirements of high-throughput DMF chips, especially for scenarios such as droplet digital PCR and single-cell genomics that require temperature control for a large number of droplets. , These scenarios require the consideration of the planar and vertical temperature distribution inside the chip, which has not been previously studied. Therefore, in DMF technology, an open thermal control system that ensures precise temperature control over a wide range is desirable.…”
Section: Introductionmentioning
confidence: 99%
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“…However, with the development of the digital microfluidic technology, the number of electrodes has been further increased to achieve higher parallel processing capabilities. In our previous work, the number of electrodes in a chip was 4096, with a single droplet volume of 10 nL. , Existing temperature control methods cannot meet the requirements of high-throughput DMF chips, especially for scenarios such as droplet digital PCR and single-cell genomics that require temperature control for a large number of droplets. , These scenarios require the consideration of the planar and vertical temperature distribution inside the chip, which has not been previously studied. Therefore, in DMF technology, an open thermal control system that ensures precise temperature control over a wide range is desirable.…”
Section: Introductionmentioning
confidence: 99%
“…In our previous work, the number of electrodes in a chip was 4096, with a single droplet volume of 10 nL. 22 , 23 Existing temperature control methods cannot meet the requirements of high-throughput DMF chips, especially for scenarios such as droplet digital PCR and single-cell genomics that require temperature control for a large number of droplets. 24 , 25 These scenarios require the consideration of the planar and vertical temperature distribution inside the chip, which has not been previously studied.…”
Section: Introductionmentioning
confidence: 99%