作者
Jinyue Bai,Peiyong Jiang,Lu Ji,W. K. Lam,Qing Zhou,L. Mary‐Jane,Spencer C. Ding,Saravanan Ramakrishnan,Chun Wai Wan,Tongxin Claire Yang,Masashi Yukawa,Rebecca W. Y. Chan,Rong Qiao,Stephanie C Y Yu,L. Y. Lois Choy,Yuwei Shi,Zilong Wang,Tommy H. C. Tam,Man Fai Law,Raymond Wong,John Wong,Stephen L. Chan,Grace Lai‐Hung Wong,Vincent Wai‐Sun Wong,K.C. Allen Chan,Y. M. Dennis Lo
摘要
The analysis of tissues of origin of cell-free DNA (cfDNA) is of research and diagnostic interest. Many studies focused on bisulfite treatment or immunoprecipitation protocols to assess the tissues of origin of cfDNA. DNA loss often occurs during such processes. Fragmentomics of cfDNA molecules has uncovered a wealth of information related to tissues of origin of cfDNA. There is still much room for the development of tools for assessing contributions from various tissues into plasma using fragmentomic features. Hence, we developed an approach to analyze the relative contributions of DNA from different tissues into plasma, by identifying characteristic fragmentation patterns associated with selected histone modifications. We named this technique as FRAGmentomics-based Histone modification Analysis (FRAGHA). Deduced placenta-specific histone H3 lysine 27 acetylation (H3K27ac)-associated signal correlated well with the fetal DNA fraction in maternal plasma (Pearson's