標(biāo)題: Titlebook: Clinical Applications of PCR; Rajyalakshmi Luthra,Rajesh R. Singh,Keyur P. Patel Book 2016Latest edition Springer Science+Business Media N [打印本頁] 作者: ARSON 時(shí)間: 2025-3-21 19:59
書目名稱Clinical Applications of PCR影響因子(影響力)
書目名稱Clinical Applications of PCR影響因子(影響力)學(xué)科排名
書目名稱Clinical Applications of PCR網(wǎng)絡(luò)公開度
書目名稱Clinical Applications of PCR網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Clinical Applications of PCR被引頻次
書目名稱Clinical Applications of PCR被引頻次學(xué)科排名
書目名稱Clinical Applications of PCR年度引用
書目名稱Clinical Applications of PCR年度引用學(xué)科排名
書目名稱Clinical Applications of PCR讀者反饋
書目名稱Clinical Applications of PCR讀者反饋學(xué)科排名
作者: 該得 時(shí)間: 2025-3-21 21:37 作者: archetype 時(shí)間: 2025-3-22 02:06 作者: bibliophile 時(shí)間: 2025-3-22 06:43
Emulsion PCR: Techniques and Applications, is dilution and compartmentalization of template molecules in water droplets in a water-in-oil emulsion. Ideally, the dilution is to a degree where each droplet contains a single template molecule and functions as a micro-PCR reactor. Here, we discuss the basic principles, advantages, and challenge作者: 集中營(yíng) 時(shí)間: 2025-3-22 12:44
Quantitative PCR for Plasma Epstein-Barr Virus Loads in Cancer Diagnostics,Hodgkin’s lymphoma, Burkitt’s lymphoma, nasopharyngeal carcinoma, and HIV-related lymphomas. It infects nearly all humans and then persists for the life of the host in a small proportion of benign B lymphocytes. EBV reactivation, usually in the setting of immunosuppression, is the main risk factor f作者: Peak-Bone-Mass 時(shí)間: 2025-3-22 16:39
High-Resolution Melt Curve Analysis in Cancer Mutation Screen,f mutated versus wild-type DNA sequences. HRM analysis is a high-throughput, sensitive, and efficient alternative to Sanger sequencing and is used to assess for mutations in clinically important genes involved in cancer diagnosis. The technique involves PCR amplification of a target sequence in the 作者: Peak-Bone-Mass 時(shí)間: 2025-3-22 20:10
Locked Nucleic Acid Probes (LNA) for Enhanced Detection of Low-Level, Clinically Significant Mutatiral high sensitivity methods are described, the incorporation of these new techniques in a clinical lab may be difficult if the technology is not readily available or requires major changes in the workflow of the laboratory. Techniques that are robust and easily adapted to existing laboratory protoc作者: accomplishment 時(shí)間: 2025-3-22 21:52
Genotyping of Frequent Mutations in Solid Tumors by PCR-Based Single-Base Extension and MassARRAY As has greatly impacted the clinical care of cancer patients based on the fact that many of these tumors exhibit activating mutations in driver genes that are prone to target therapy, largely impacting cancer management strategies. Genomic heterogeneity of tumors is becoming an increasingly recognize作者: 收集 時(shí)間: 2025-3-23 05:17 作者: infatuation 時(shí)間: 2025-3-23 08:12 作者: Additive 時(shí)間: 2025-3-23 11:43 作者: Enzyme 時(shí)間: 2025-3-23 15:48
PCR Techniques in Next-Generation Sequencing,high demand. This is not the case however, as PCR techniques play an important role in the success of NGS technology. Although NGS has rapidly become an important part of clinical molecular diagnostics, whole genome sequencing is still difficult to implement in a clinical laboratory due to high cost作者: 歡騰 時(shí)間: 2025-3-23 20:33 作者: hardheaded 時(shí)間: 2025-3-24 02:03
Quantitative Real-Time PCR: Recent Advances,ss takes place in real time in a “closed-tube” system. Although this technique can provide an absolute quantification of the initial template copy number, quantification relative to a control sample or second sequence is typically adequate. The quantification process employs melting curve analysis a作者: inchoate 時(shí)間: 2025-3-24 03:08 作者: 夾死提手勢(shì) 時(shí)間: 2025-3-24 10:01
Book 2016Latest editionnfectious diseases, estimation of gene copy number aberrations, primer extension coupled with mass spectroscopy, and high throughput NGS techniques. The application of PCR has shown incredible value in the study of genomics and transcriptomics, not only for discovery but also for routine clinical ap作者: 急急忙忙 時(shí)間: 2025-3-24 14:18 作者: 易碎 時(shí)間: 2025-3-24 17:56 作者: mendacity 時(shí)間: 2025-3-24 20:02
War and Peace in the 21st Centuryassess for mutations in clinically important genes involved in cancer diagnosis. The technique involves PCR amplification of a target sequence in the presence of a fluorescent double-stranded DNA (dsDNA) binding dye, melting of the fluorescent amplicons, and subsequent interpretation of melt curve profiles.作者: 高度 時(shí)間: 2025-3-25 00:34
https://doi.org/10.1057/9781137433237clinical stage of the disease in which diagnosis is often challenging. This chapter describes the application of polymerase chain reaction (PCR) for the detection of . DNA including protocols for sample preparation, DNA extraction, and target amplification methods.作者: 白楊魚 時(shí)間: 2025-3-25 06:23 作者: 偽證 時(shí)間: 2025-3-25 10:22 作者: Sinus-Rhythm 時(shí)間: 2025-3-25 12:49
High-Resolution Melt Curve Analysis in Cancer Mutation Screen,assess for mutations in clinically important genes involved in cancer diagnosis. The technique involves PCR amplification of a target sequence in the presence of a fluorescent double-stranded DNA (dsDNA) binding dye, melting of the fluorescent amplicons, and subsequent interpretation of melt curve profiles.作者: 親愛 時(shí)間: 2025-3-25 19:52 作者: dithiolethione 時(shí)間: 2025-3-25 21:10 作者: 注射器 時(shí)間: 2025-3-26 03:35
Ethnicity and Geopolitics of Rohingya Crisisnrich, and whenever a mutation is suspected to be present but is undetectable using conventional PCR and sequencing methods. We describe in this chapter our COLD-PCR-based pyrosequencing method for . mutation detection in various clinical samples using DNA extracted from either fresh or fixed paraffin-embedded tissue specimens.作者: macabre 時(shí)間: 2025-3-26 05:35
Michael Blain,Angeline Kearns-Blainon Sphere? Particles (ISPs) on the Ion Personal Genome Machine. (PGM?) System. For routine clinical testing, following library generation, we employ the automated Ion OneTouch? System that includes the Ion OneTouch? 2 and the Ion OneTouch? ES instruments for template generation and enrichment of template-positive ISPs, respectively.作者: TOXIC 時(shí)間: 2025-3-26 09:03 作者: Expand 時(shí)間: 2025-3-26 16:08
Reconceptualised Security in MexicoR and single molecular emulsion PCR for genotyping, gene expression, and miRNA expression. In this chapter, the use of a microfluidics-based PCR for simultaneous screening of 14 known fusion transcripts in patients with leukemia is described.作者: ZEST 時(shí)間: 2025-3-26 20:46 作者: 收藏品 時(shí)間: 2025-3-26 22:13
Emulsion PCR: Techniques and Applications,on Sphere? Particles (ISPs) on the Ion Personal Genome Machine. (PGM?) System. For routine clinical testing, following library generation, we employ the automated Ion OneTouch? System that includes the Ion OneTouch? 2 and the Ion OneTouch? ES instruments for template generation and enrichment of template-positive ISPs, respectively.作者: 貪婪性 時(shí)間: 2025-3-27 02:17 作者: 同位素 時(shí)間: 2025-3-27 08:57 作者: 抵押貸款 時(shí)間: 2025-3-27 11:07
Genotyping of Frequent Mutations in Solid Tumors by PCR-Based Single-Base Extension and MassARRAY Ad phenomenon relevant to genome-based medicine. Because a large number tumors may display several mutations at the same time, multiplexing has become the preferred approach to reveal the mutational landscape in patient samples and to better design a targeted approach to their illness.作者: 駕駛 時(shí)間: 2025-3-27 14:11
Polymerase Chain Reaction Diagnosis of Leishmaniasis: A Species-Specific Approach,tion of polymerase chain reaction (PCR) in the detection of . parasites across the disease spectrum, including protocols for sample collection and transportation, genomic material extraction, and target amplification methods with special emphasis on PCR amplification of the cytochrome . gene for .. species identification.作者: 千篇一律 時(shí)間: 2025-3-27 18:53
Quantitative Real-Time PCR: Recent Advances,nd/or fluorescent detection systems and can provide amplification and genotyping in a relatively short time. Here we describe the properties and uses of various fluorescent detection systems used for quantification.作者: 睨視 時(shí)間: 2025-3-27 22:50 作者: critic 時(shí)間: 2025-3-28 02:48 作者: 熱烈的歡迎 時(shí)間: 2025-3-28 07:05
Book 2016Latest editionotocols, and tips on troubleshooting and avoiding known pitfalls...Thorough and authoritative, .Clinical Applications of PCR, Third Edition. serves as an ideal guide for researchers aiming to understand the principles behind each application and for their implementation in the laboratory..作者: homocysteine 時(shí)間: 2025-3-28 14:11
https://doi.org/10.1007/978-3-319-73808-6d phenomenon relevant to genome-based medicine. Because a large number tumors may display several mutations at the same time, multiplexing has become the preferred approach to reveal the mutational landscape in patient samples and to better design a targeted approach to their illness.作者: 燒烤 時(shí)間: 2025-3-28 16:21 作者: 不來 時(shí)間: 2025-3-28 20:13
Critical Cultural Studies of Childhoodnd/or fluorescent detection systems and can provide amplification and genotyping in a relatively short time. Here we describe the properties and uses of various fluorescent detection systems used for quantification.作者: 抓住他投降 時(shí)間: 2025-3-28 23:10
A Targeted Q-PCR-Based Method for Point Mutation Testing by Analyzing Circulating DNA for Cancer Maservations made on the specific structure and size of cfDNA. It enables the simultaneous determination of five parameters: the cfDNA total concentration, the presence of a previously known point mutation, the mutant (tumor) cfDNA concentration (ctDNA), the proportion of mutant cfDNA, and the cfDNA f作者: 薄荷醇 時(shí)間: 2025-3-29 06:29
Quantitative PCR for Plasma Epstein-Barr Virus Loads in Cancer Diagnostics,t studies have shown that EBV genomic DNA can be detected in blood of patients with EBV-associated diseases, and that monitoring of EBV viral load in blood could be an effective method of distinguishing disease-associated EBV reactivation from incidental EBV present in benign B lymphocytes, and coul作者: hauteur 時(shí)間: 2025-3-29 08:55
PCR Techniques in Characterizing DNA Methylation,ulfite treatment. Variations of this method include bisulfite sequencing, methylation-specific PCR, real-time PCR-based MethyLight, and methylation-sensitive high-resolution melting PCR. Several whole-epigenome profiling technologies such as MethylC-seq reduced representation bisulfite sequencing (R作者: Blanch 時(shí)間: 2025-3-29 11:44
Steven Ratuva,Hamdy A. Hassan,Radomir Compelservations made on the specific structure and size of cfDNA. It enables the simultaneous determination of five parameters: the cfDNA total concentration, the presence of a previously known point mutation, the mutant (tumor) cfDNA concentration (ctDNA), the proportion of mutant cfDNA, and the cfDNA f作者: ligature 時(shí)間: 2025-3-29 17:23
SpringerBriefs in Information Systemst studies have shown that EBV genomic DNA can be detected in blood of patients with EBV-associated diseases, and that monitoring of EBV viral load in blood could be an effective method of distinguishing disease-associated EBV reactivation from incidental EBV present in benign B lymphocytes, and coul作者: legislate 時(shí)間: 2025-3-29 20:38
Negative Consequences of Protectionulfite treatment. Variations of this method include bisulfite sequencing, methylation-specific PCR, real-time PCR-based MethyLight, and methylation-sensitive high-resolution melting PCR. Several whole-epigenome profiling technologies such as MethylC-seq reduced representation bisulfite sequencing (R作者: Neonatal 時(shí)間: 2025-3-30 01:54 作者: 大漩渦 時(shí)間: 2025-3-30 04:35 作者: Infiltrate 時(shí)間: 2025-3-30 11:19
