作者
Mirazul Islam,Yilin Yang,Alan J. Simmons,Vishal M. Shah,Musale Krushna Pavan,Yanwen Xu,Naila Tasneem,Zhengyi Chen,Linh T. Trinh,Paola Molina,Marisol Ramirez‐Solano,Iannish Sadien,Jinzhuang Dou,Ken Chen,Mark A. Magnuson,Jeffrey C. Rathmell,Ian G. Macara,Douglas J. Winton,Qi Liu,Hamim Zafar,Reza Kalhor,George M. Church,Martha J. Shrubsole,Robert J. Coffey,Ken S. Lau
摘要
Key to understanding many biological phenomena is knowing the temporal ordering of cellular events, which often require continuous direct observations [1, 2]. An alternative solution involves the utilization of irreversible genetic changes, such as naturally occurring mutations, to create indelible markers that enables retrospective temporal ordering [3-8]. Using NSC-seq, a newly designed and validated multi-purpose single-cell CRISPR platform, we developed a molecular clock approach to record the timing of cellular events and clonality