循环肿瘤DNA
计算生物学
个性化医疗
循环肿瘤细胞
生物标志物
癌症研究
肿瘤科
医学
生物
癌症
生物信息学
内科学
遗传学
转移
作者
Iver Nordentoft,Karin Birkenkamp‐Demtröder,Lars Dyrskjøt
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 179-197
被引量:2
标识
DOI:10.1007/978-1-0716-3291-8_11
摘要
Accurate circulating tumor DNA (ctDNA) detection has an immense biomarker potential in all phases of the cancer disease course. Presence of ctDNA in the blood has been shown to have prognostic value in various cancer types as it may reflect the actual tumor burden. There are two main methods to consider, a tumor-informed and a tumor-agnostic analysis of ctDNA. Both techniques exploit the short half-life of circulating cell-free DNA (cfDNA)/ctDNA for disease monitoring and ultimately future clinical treatment intervention. Urothelial carcinoma is characterized by a high mutation spectrum but very few hotspot mutations. This limits tumor agnostic usability of hotspot mutation or fixed sets of genes for ctDNA detection. Here we focus on a tumor-informed analysis for ultrasensitive patient- and tumor-specific ctDNA detection using personalized mutation panels, probes that bind to specific genomic sequences to enrich for the region of interest. In this chapter, we describe methods for purification of high-quality cfDNA and guidelines for designing tumor-informed customized capture panels for sensitive detection of ctDNA. Furthermore, a detailed protocol for library preparation and panel capture utilizing a double enrichment strategy with low amplification is described.
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