期刊文献+

基于NTC热敏电阻器的实时PCR仪数据采集器设计 被引量:5

Design of data acquisition in real-time PCR instrument based on NTC thermistor
在线阅读 下载PDF
导出
摘要 实时聚合酶链反应(PCR)是一种通过热循环与荧光信号检测方法实现特定DNA片段的快速复制与定量检测的技术。PCR反应过程中,热循环温度控制精度决定了PCR反应效率,从而直接影响定量检测的精度。根据非稳态传热原理,热量从基座传递到试液需要一定的时间,为了检测这一延迟时间对温控的影响,基于NTC热敏电阻器,采用USB总线和FPGA技术,以USB控制器和FPGA为核心控制模块,AD7663为模数转换芯片,实现数据采集器的设计,并采用多线程技术和缓冲队列方法实现连续数据采集。通过理论与实验相结合,准确测量了试液升降温过程中的延迟时间,对实时PCR仪温度控制具有重要意义。 Real-time polymerase chain reaction(PCR) is a method for rapid replication and quantitative detection of specific DNA fragment through thermal cycle and fluorescent signal detection.The precision of temperature control in thermal cycle determines PCR efficiency,and also affects the precision of quantitative detection.According to the theory of unsteady state heat transfer,heat takes time to transfer from block to test solution.In order to know the influence of the delay time on temperature control,a data acquisition has been designed using USB bus and FPGA technology based on NTC thermistor,and continuous data acquisition is achieved through multi-threading technology and buffering queues.By the combination of theory and experiment,the delay time of heat transfer has been measured successfully.
出处 《传感器与微系统》 CSCD 北大核心 2011年第3期114-117,共4页 Transducer and Microsystem Technologies
关键词 聚合酶链反应 热敏电阻器 USB总线 现场可编程门阵列 数据采集 缓冲队列 polymerase chain reaction(PCR) thermistor USB bus field programmable gate array(FPGA) data acquisition buffering queues
作者简介 刘娟容(1984-),女,湖南邵东人,硕士研究生,主要研究方向为信号处理、生物医学仪器。
  • 相关文献

参考文献5

二级参考文献27

  • 1张和生,王立文.一种高精度数据采集系统的电路设计[J].计算机测量与控制,2004,12(6):575-577. 被引量:14
  • 2张波,常天庆,贾宇飞.基于USB技术的数据采集卡设计[J].微计算机信息,2006(06Z):34-36. 被引量:11
  • 3徐锋.基于FT245BM的快速USB接口设计[J].电子工程师,2007,33(3):59-61. 被引量:13
  • 4Joseph J.PCR—based detection and quantification of tapesia yallundae and tapesia acuformis[P].US:6319673,11,2001.
  • 5Mathies R.Process for microfabrication of an integrated PCR—CE device and products produced by the same[P].US:6261431,2001.
  • 6Staczek J.Low—frequency electromagnetic fields alter the replication cycle of MS2 bacteriophage[J].Current Microbiology,1998,36(3):298—301.
  • 7Joseph J. PCR-based detection and quantification of tapesia yallundae and tapesia acuformis[P]. US:6319673, 11,2001.
  • 8Mathies R. Process for microfabrication of an integrated PCR-CE device and products produced by the same[P]. US: 6261431, 2001.
  • 9Staczek J. Low-frequency electromagnetic fields alter the replication cycle of MS2 bacteriophage[J]. Current Microbiology, 1998, 36(3):298-301.
  • 10Quinn T J.Temperature[M].New York:Academic Press Inc,1983.231-235.

共引文献45

同被引文献52

引证文献5

二级引证文献25

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部