{"title":"可降解微流体生物芯片的缺陷容忍度","authors":"Fei Su, K. Chakrabarty","doi":"10.1109/VTS.2005.39","DOIUrl":null,"url":null,"abstract":"Defect tolerance is an important design consideration for microfluidics-based biochips that are used for safety-critical applications. We propose a defect tolerance methodology based on graceful degradation and dynamic reconfiguration. We first introduce tile-based biochip architecture, which is scalable for large-scale bioassays. A clustered defect model is used to evaluate the graceful degradation method for tile-based biochips. The proposed schemes ensure that the bioassays mapped to a droplet-based microfluidic array during design can be executed on a defective biochip through operation rescheduling and/or resource rebinding. Real-life biochemical procedures, namely polymerase chain reaction (PCR) and multiplexed in-vitro diagnostics on human physiological fluids, are used to evaluate the proposed defect tolerance schemes.","PeriodicalId":268324,"journal":{"name":"23rd IEEE VLSI Test Symposium (VTS'05)","volume":"62 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2005-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"25","resultStr":"{\"title\":\"Defect tolerance for gracefully-degradable microfluidics-based biochips\",\"authors\":\"Fei Su, K. Chakrabarty\",\"doi\":\"10.1109/VTS.2005.39\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Defect tolerance is an important design consideration for microfluidics-based biochips that are used for safety-critical applications. We propose a defect tolerance methodology based on graceful degradation and dynamic reconfiguration. We first introduce tile-based biochip architecture, which is scalable for large-scale bioassays. A clustered defect model is used to evaluate the graceful degradation method for tile-based biochips. The proposed schemes ensure that the bioassays mapped to a droplet-based microfluidic array during design can be executed on a defective biochip through operation rescheduling and/or resource rebinding. Real-life biochemical procedures, namely polymerase chain reaction (PCR) and multiplexed in-vitro diagnostics on human physiological fluids, are used to evaluate the proposed defect tolerance schemes.\",\"PeriodicalId\":268324,\"journal\":{\"name\":\"23rd IEEE VLSI Test Symposium (VTS'05)\",\"volume\":\"62 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"25\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"23rd IEEE VLSI Test Symposium (VTS'05)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/VTS.2005.39\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"23rd IEEE VLSI Test Symposium (VTS'05)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/VTS.2005.39","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Defect tolerance for gracefully-degradable microfluidics-based biochips
Defect tolerance is an important design consideration for microfluidics-based biochips that are used for safety-critical applications. We propose a defect tolerance methodology based on graceful degradation and dynamic reconfiguration. We first introduce tile-based biochip architecture, which is scalable for large-scale bioassays. A clustered defect model is used to evaluate the graceful degradation method for tile-based biochips. The proposed schemes ensure that the bioassays mapped to a droplet-based microfluidic array during design can be executed on a defective biochip through operation rescheduling and/or resource rebinding. Real-life biochemical procedures, namely polymerase chain reaction (PCR) and multiplexed in-vitro diagnostics on human physiological fluids, are used to evaluate the proposed defect tolerance schemes.