生物
亚硫酸氢盐测序
亚硫酸氢盐
DNA
多重位移放大
计算生物学
DNA测序
甲基化DNA免疫沉淀
DNA甲基化
基因组
癌症
分子生物学
单细胞测序
胎儿游离DNA
聚合酶链反应
遗传学
基因
DNA提取
突变
外显子组测序
基因表达
胎儿
产前诊断
怀孕
作者
Xiao‐Long Cui,Ji Nie,Houxiang Zhu,Krissana Kowitwanich,Alana V. Beadell,Diana C. West-Szymanski,Zhou Zhang,Urszula Dougherty,Akushika Kwesi,Zifeng Deng,Yan Li,Danqing Meng,Kevin K. Roggin,Teresa Barry,Ryan C. Owyang,Ben Fefferman,Chang Zeng,Lu Gao,Carolyn W. T. Zhao,Yuri Malina
标识
DOI:10.1186/s13059-024-03262-2
摘要
Methylation-based liquid biopsies show promises in detecting cancer using circulating cell-free DNA; however, current limitations impede clinical application. Most assays necessitate substantial DNA inputs, posing challenges. Additionally, underrepresented tumor DNA fragments may go undetected during exponential amplification steps of traditional sequencing methods. Here, we report linear amplification-based bisulfite sequencing (LABS), enabling linear amplification of bisulfite-treated DNA fragments in a genome-wide, unbiased fashion, detecting cancer abnormalities with sub-nanogram inputs. Applying LABS to 100 patient samples revealed cancer-specific patterns, copy number alterations, and enhanced cancer detection accuracy by identifying tissue-of-origin and immune cell composition.
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