標(biāo)題: Titlebook: Clinical Applications of Nucleic Acid Amplification; Meagan B. Myers,Cynthia A. Schandl Book 2023 The Editor(s) (if applicable) and The Au [打印本頁] 作者: 關(guān)稅 時(shí)間: 2025-3-21 19:18
書目名稱Clinical Applications of Nucleic Acid Amplification影響因子(影響力)
書目名稱Clinical Applications of Nucleic Acid Amplification影響因子(影響力)學(xué)科排名
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書目名稱Clinical Applications of Nucleic Acid Amplification網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Clinical Applications of Nucleic Acid Amplification被引頻次
書目名稱Clinical Applications of Nucleic Acid Amplification被引頻次學(xué)科排名
書目名稱Clinical Applications of Nucleic Acid Amplification年度引用
書目名稱Clinical Applications of Nucleic Acid Amplification年度引用學(xué)科排名
書目名稱Clinical Applications of Nucleic Acid Amplification讀者反饋
書目名稱Clinical Applications of Nucleic Acid Amplification讀者反饋學(xué)科排名
作者: Proponent 時(shí)間: 2025-3-21 23:26
Meagan B. Myers,Cynthia A. SchandlIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts作者: 禁止,切斷 時(shí)間: 2025-3-22 01:15 作者: 無聊的人 時(shí)間: 2025-3-22 06:46 作者: MILL 時(shí)間: 2025-3-22 12:26
978-1-0716-2952-9The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines作者: 指數(shù) 時(shí)間: 2025-3-22 13:56 作者: 指數(shù) 時(shí)間: 2025-3-22 17:28
Current Status of Functional Neurosurgery can be generated to allow the study of these regions. Fields that use this technology range from forensics to the experimental study of human biology. Standards for performing PCR and information tools to help design PCR protocols aid in successful implementation of PCR.作者: 職業(yè) 時(shí)間: 2025-3-22 23:37
Current Status of Functional Neurosurgery can be generated to allow the study of these regions. Fields that use this technology range from forensics to the experimental study of human biology. Standards for performing PCR and information tools to help design PCR protocols aid in successful implementation of PCR.作者: Calibrate 時(shí)間: 2025-3-23 03:45 作者: 物種起源 時(shí)間: 2025-3-23 08:02
Treatment of Traumatic Cavernous Fistulases unique implementations in all aspects of the assay, including the wet bench, bioinformatics, and reporting. Following implementation, the informatics of many of these tests continue to change over time, from software and annotation source updates, guidelines, and knowledgebase changes to changes 作者: 不真 時(shí)間: 2025-3-23 10:00
Lecture Notes in Computer Scienceiopsies. This has coincided with the development of techniques that allow the detection of low-frequency allele variants in clinical samples that typically carry very low amounts of fragmented DNA, such as plasma or FFPE samples. Enrichment of rare variants by nuclease-assisted mutant allele enrichm作者: RAG 時(shí)間: 2025-3-23 14:57 作者: fibroblast 時(shí)間: 2025-3-23 18:33
Andrew Chester,Yun Sing Koh,Junjae Leede fashion. Frequently, patient-derived tissues stored in long-term hospital tissue banks have been preserved using formalin-fixation paraffin-embedding (FFPE). While these samples can comprise valuable resources for studying disease, the fixation process ultimately compromises the DNA’s integrity a作者: 連鎖 時(shí)間: 2025-3-23 22:12 作者: Outshine 時(shí)間: 2025-3-24 03:37
Po Chan Chiu,Ali Selamat,Ondrej KrejcarAypar et al., Eur J Haematol 102(1):87–96, 2019; Smadbeck et al., Blood Cancer J 9(12):103, 2019) and are particularly helpful in characterizing genomic rearrangements. Mate pair sequencing (MPseq) leverages a unique library preparation chemistry involving circularization of long DNA fragments, allo作者: humectant 時(shí)間: 2025-3-24 06:33 作者: BLA 時(shí)間: 2025-3-24 14:43 作者: 權(quán)宜之計(jì) 時(shí)間: 2025-3-24 14:54
Xin Huang,Huilin Song,Mingming Lu genetic diseases. Rapid whole genome sequencing (rWGS), including sample preparation, short-read sequencing-by-synthesis, informatics pipelining, and semiautomated interpretation, can now identify nucleotide and structural variants associated with most genetic diseases with robust analytic and diag作者: 充滿人 時(shí)間: 2025-3-24 20:41
Path Inference Based on Voronoi Graphan include alterations of complete chromosomes. As CNVs mean the gain or loss of DNA sequences, their detection requires specific techniques and analysis. We have developed Easy One-Step Amplification and Labeling for CNV Detection (EOSAL–CNV) by fragment analysis in a DNA sequencer. The procedure i作者: faddish 時(shí)間: 2025-3-25 02:05 作者: Corral 時(shí)間: 2025-3-25 05:01
Book 2023aboratory protocols, and tips on troubleshooting and avoiding known pitfalls. ..Cutting-edge and thorough, .Clinical Applications of Nucleic Acid Amplification. is a valuable resource for both novice and expert scientists in this developing field. .作者: Defense 時(shí)間: 2025-3-25 09:04 作者: 陶器 時(shí)間: 2025-3-25 13:44 作者: amygdala 時(shí)間: 2025-3-25 18:22 作者: acrophobia 時(shí)間: 2025-3-25 20:22
Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Childd can improve outcomes. Since first described 10?years ago, rWGS has evolved considerably. Here we describe our current methods for routine diagnostic testing for genetic diseases by rWGS in as little as 18?h.作者: 凌辱 時(shí)間: 2025-3-26 03:32
1064-3745 ation advice from the experts.This volume details applications, methods, and protocols on nucleic acid amplification. Chapters detail the management of organ and stem cell transplantation, constitutional genetics and genomics, epidemiology, public health, nucleic acid detection, methods for amplific作者: machination 時(shí)間: 2025-3-26 07:49
Managing a PCR Contamination Event in a Molecular Pathology Laboratoryt cause analysis to determine the source of contamination, and assess and document the results of the decontamination process will be reviewed. Finally, the chapter will discuss a return to normal with consideration of appropriate corrective actions to mitigate future contamination events.作者: Ventricle 時(shí)間: 2025-3-26 12:14 作者: 并入 時(shí)間: 2025-3-26 15:15 作者: peptic-ulcer 時(shí)間: 2025-3-26 19:39 作者: inflate 時(shí)間: 2025-3-26 22:02
Current Status of Functional Neurosurgeryt cause analysis to determine the source of contamination, and assess and document the results of the decontamination process will be reviewed. Finally, the chapter will discuss a return to normal with consideration of appropriate corrective actions to mitigate future contamination events.作者: FAST 時(shí)間: 2025-3-27 02:09 作者: ADORN 時(shí)間: 2025-3-27 07:41 作者: Adornment 時(shí)間: 2025-3-27 12:11 作者: 幸福愉悅感 時(shí)間: 2025-3-27 14:17 作者: Generic-Drug 時(shí)間: 2025-3-27 17:49 作者: heirloom 時(shí)間: 2025-3-28 00:10 作者: 鬼魂 時(shí)間: 2025-3-28 02:05
Next-Generation Sequencing Informatic Architecture Considerationses unique implementations in all aspects of the assay, including the wet bench, bioinformatics, and reporting. Following implementation, the informatics of many of these tests continue to change over time, from software and annotation source updates, guidelines, and knowledgebase changes to changes 作者: monopoly 時(shí)間: 2025-3-28 07:29
Nuclease Enrichment and qPCR Detection of Rare Nucleotide Variantsiopsies. This has coincided with the development of techniques that allow the detection of low-frequency allele variants in clinical samples that typically carry very low amounts of fragmented DNA, such as plasma or FFPE samples. Enrichment of rare variants by nuclease-assisted mutant allele enrichm作者: infinite 時(shí)間: 2025-3-28 11:38 作者: Kidnap 時(shí)間: 2025-3-28 17:21 作者: 季雨 時(shí)間: 2025-3-28 20:57 作者: 無所不知 時(shí)間: 2025-3-29 02:25
Mate Pair Sequencing: Next-Generation Sequencing for Structural Variant DetectionAypar et al., Eur J Haematol 102(1):87–96, 2019; Smadbeck et al., Blood Cancer J 9(12):103, 2019) and are particularly helpful in characterizing genomic rearrangements. Mate pair sequencing (MPseq) leverages a unique library preparation chemistry involving circularization of long DNA fragments, allo作者: Fermentation 時(shí)間: 2025-3-29 03:37 作者: craven 時(shí)間: 2025-3-29 07:51 作者: Cerebrovascular 時(shí)間: 2025-3-29 12:23
Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Child genetic diseases. Rapid whole genome sequencing (rWGS), including sample preparation, short-read sequencing-by-synthesis, informatics pipelining, and semiautomated interpretation, can now identify nucleotide and structural variants associated with most genetic diseases with robust analytic and diag作者: gonioscopy 時(shí)間: 2025-3-29 19:34 作者: conspicuous 時(shí)間: 2025-3-29 19:48
Rapid Cycle and Extreme Polymerase Chain Reactionce quality for speed; sensitivity, specificity, and yield are equivalent or better than conventional PCR. What is required (and not widely available) is rapid, accurate control of reaction temperature during cycling. Specificity improves with cycling speed, and efficiency can be maintained by increa作者: 相反放置 時(shí)間: 2025-3-30 02:03 作者: 博識(shí) 時(shí)間: 2025-3-30 04:17 作者: relieve 時(shí)間: 2025-3-30 09:27
Andrew Chester,Yun Sing Koh,Junjae Lee MRE-seq correlate well (0.92) with traditional MRE-seq calls when profiling non-degraded samples, and can recover unmethylated regions in highly degraded samples when traditional MRE-seq fails, which we validate using bisulfite sequencing-based data (WGBS) as well as methylated DNA immunoprecipitat
