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Titlebook: Cell-free DNA as Diagnostic Markers; Methods and Protocol Valentina Casadio,Samanta Salvi Book 2019 Springer Science+Business Media, LLC, p

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楼主: digestive-tract
发表于 2025-3-26 21:09:32 | 显示全部楼层
Circulating Cell-Free DNA and Cancer Therapy Monitoring: Methods and Potentialresence of possible metastasis, (4) a marker of the success of secondary subsequent treatment, (5) determining which patients can benefit from a particular treatment, and (6) offering a prognosis. These aspects will be discussed concerning the application of circulating tumor DNA analysis to the monitoring of cancer patients undergoing therapy.
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Copy Number Variation Analysis on Cell-Free Serum DNANVs in circulating, cell-free DNA by multiplex ligation-dependent probe amplification (MLPA). MLPA represents an efficient method for the detection of CNVs among numerous genes on various chromosomal regions in serum.
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dPCR Mutational Analyses in Cell-Free DNA: A Comparison with Tissuese consists of a pair of primers and two probes labeled with a fluorescent dye capable to recognize the presence or absence of a specific mutation. Using the dPCR method, we can identify only a few mutations in tissue that are present also in plasma.
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Quantitative Methylation-Specific PCR: A Simple Method for Studying Epigenetic Modifications of Cellue that can be easily implemented into clinical practice. In this chapter, we provide a detailed protocol for SYBR Green qMSP analysis which is currently used in our laboratory for cfDNA methylation detection. Useful information regarding successful qMSP primers design are also provided.
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Studying Copy Number Variations in Cell-Free DNA: The Example of AR in Prostate Cancerrting from the hypothesis that the gain of androgen receptor (.) gene is a frequent aberration in advanced prostate cancer patients, we analyzed it in cfDNA as a potential predictive biomarker of specific treatments. Here we report a general protocol that may be considered to analyze gene copy number variations in serum or plasma fluids.
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Observer-Based Fault Estimation Techniquesasive disease biomarker. The interest in clinical applications has gained an exponential increase, making it a popular and potential target in a wide range of research areas..cfDNA can be found in different body fluids, both in healthy and not healthy subjects. The recent and rapid development of ne
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Christian Müller-Schloer,Sven Tomfordeimportant to optimize pre-analytical and analytical procedures in order to maximize the performance of cfDNA-based analyses..In this chapter, we report the most common methods for the correct collection, centrifugation, storage, and DNA isolation from cell-free biological sources such as plasma, uri
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https://doi.org/10.1007/978-3-319-68938-8either approach has the sensitivity or specificity to be very sure of the efficacy of the treatment. Moreover, PET/CT scans can be both comparatively expensive and produce low levels of radiation for the patient. The advent of the possibility of using circulating DNA released from the tumor permits
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Oaks and People: A Long Journey Together,ch show a source of potential biomarkers. In cancer patients, it is a simple and less invasive mean, representing a sustainable alternative to interrogate all tumor cells longitudinally, quantifying and characterizing the biological materials (DNAs, RNAs, proteins) which originate from cancer tissue
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