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作 者:刘东来[1] 张春涛[1] LIU Dong-lai ZHANG Chun-tao(Division of 2nd IVD, National Institute for Food and Drug Control, Key Laboratory of the Ministry of Health for Research on Quality and Standardization of Biotech Products, Beijing 100050, China)
机构地区:[1]中国食品药品检定研究院体外诊断试剂二室卫生部生物技术产品检定方法及其标准化重点实验室,北京100050
出 处:《中国病毒病杂志》2016年第1期72-77,共6页Chinese Journal of Viral Diseases
基 金:国家高技术研究发展计划(863计划)(2011AA02A115)
摘 要:传染病是人类健康的重要威胁之一,及时准确地鉴定病原微生物,对流行病和突发疫情的防控具有重要意义。近年来,传染病诊断领域正面临新的技术革命,主角正是"下一代测序(next-generation sequencing,NGS)"技术,又称"大规模平行测序(massively parallel sequencing,MPS)"或"高通量测序(high-throughput sequencing,HTS)"技术[1-2]。与"上一代"测序(如Sanger测序)最大的不同在于,Infectious diseases have been one of the most important threat to human health all the time.Recently,next-generation sequencing(NGS)technologies have been increasingly used for diagnosis and made a revolution for infectious disease diagnostics.As the revolutionary detection technology,NGS had many irreplaceable advantages that made it play important roles in many fields such as prevention and control of epidemic of infectious diseases,detection of pathogenic microbes,identification of suspected targets,and the metagenomics.Due to some technical and regulation policy issues,NGS has not been popularized in clinical applications.However,there is no doubt that NGS would replace the traditional method for clinical diagnosis in the near future.On December 2015,BioMérieux and Illumina announced the launch of bioMérieux EpiSeq in Europe,an innovative NGS application dedicated to the epidemiological monitoring and control of healthcare-associated infections.The launch of EpiSeq was again the proof of a positive future for NGS.In this review,we briefly summarize the cutting-edge applications and challenges of NGS for detection of pathogenic microbes including viruses,bacterial,drug-resistant variants.We also introduce the current thinking of FDA regarding the management and regulation on NGS.These information could be useful for practitioners in the field of in vitro diagnostics as well as the relevant regulatory authorities.
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