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Titlebook: Advanced Techniques in Diagnostic Microbiology; Yi-Wei Tang,Charles W. Stratton Book 20061st edition Springer-Verlag US 2006 Advanced.Diag

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發(fā)表于 2025-3-21 18:04:04 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Advanced Techniques in Diagnostic Microbiology
影響因子2023Yi-Wei Tang,Charles W. Stratton
視頻videohttp://file.papertrans.cn/147/146285/146285.mp4
發(fā)行地址Provides a comprehensive and up-to-date description of advanced methods that have evolved for the diagnosis of infectious diseases in the routine clinical microbiology laboratory.Includes supplementar
圖書(shū)封面Titlebook: Advanced Techniques in Diagnostic Microbiology;  Yi-Wei Tang,Charles W. Stratton Book 20061st edition Springer-Verlag US 2006 Advanced.Diag
影響因子.Clinical microbiologists are engaged in the field of diagnostic microbiology to determine whether pathogenic microorganisms are present in clinical specimens collected from patients with suspected infections. If microorganisms are found, these are identified and susceptibility profiles, when indicated, are determined. During the past two decades, technical advances in the field of diagnostic microbiology have made constant and enormous progress in various areas, including bacteriology, mycology, mycobacteriology, parasitology, and virology. The diagnostic capabilities of modern clinical microbiology laboratories have improved rapidly and have expanded greatly due to a technological revolution in molecular aspects of microbiology and immunology. In particular, rapid techniques for nucleic acid amplification and characterization combined with automation and user-friendly software have significantly broadened the diagnostic arsenal for the clinical microbiologist. The conventional diagnostic model for clinical microbiology has been labor-intensive and frequently required days to weeks before test results were available. Moreover, due to the complexity and length of such testing, this
Pindex Book 20061st edition
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Rabindra D. Mehta,Jani Macari Pallis; and so forth. Most of the amplicons of these applications are large (range approximately from 300 base pairs to 1500 base pairs), and the exact nucleotide sequence of the amplicoms are crucial for the results.
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Book 20061st editionpecimens collected from patients with suspected infections. If microorganisms are found, these are identified and susceptibility profiles, when indicated, are determined. During the past two decades, technical advances in the field of diagnostic microbiology have made constant and enormous progress
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PROBABILISTIC TECHNIQUES IN BIOENGINEERINGignal amplification technologies include branched DNA (bDNA) and hybrid capture (HC) assays. The bDNA method was initially developed by Chiron (Emeryville, CA, USA) and marketed by Bayer Diagnostics (Emeryville, CA, USA), and the hybrid capture method was developed and marketed by Digene Corporation (Gaithersburg, MD, USA).
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Optimizing Ball and Racket Interactionhe successfulness of . amplification of the intact organism(s) outside of the infected host. Nucleic acid–based technologies allow detection by amplification of specific microbial genetic material irrespective of viability or integrity of the organism (Nissen, 2002; Gulliken, 2004; Mackay, 2004).
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utine clinical microbiology laboratory.Includes supplementar.Clinical microbiologists are engaged in the field of diagnostic microbiology to determine whether pathogenic microorganisms are present in clinical specimens collected from patients with suspected infections. If microorganisms are found, t
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Medical Imaging and Reverse Engineering is frequently life-threatening, and blood culture to detect circulating microorganisms has been the diagnostic standard. Much of the scientific and technologic advances in blood culture were made from the 1970s to the 1990s; this chapter briefly reviews various aspects of blood culture with emphasis on automated culturing systems.
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The Zoom ADC: An Evolving Architectureroorganisms. Nucleic acid probe-based microbial identification is widely used in clinical laboratories. The probes can be used for identification of microorganism directly from the specimen, from culture, or on formalin-fixed and paraffin-embedded tissue.
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