Cargando…
High throughput PRIME editing screens identify functional DNA variants in the human genome
Despite tremendous progress in detecting DNA variants associated with human disease, interpreting their functional impact in a high-throughput and base-pair resolution manner remains challenging. Here, we develop a novel pooled prime editing screen method, PRIME, which can be applied to characterize...
Autores principales: | Ren, Xingjie, Yang, Han, Nierenberg, Jovia L., Sun, Yifan, Chen, Jiawen, Beaman, Cooper, Pham, Thu, Nobuhara, Mai, Takagi, Maya Asami, Narayan, Vivek, Li, Yun, Ziv, Elad, Shen, Yin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370011/ https://www.ncbi.nlm.nih.gov/pubmed/37502948 http://dx.doi.org/10.1101/2023.07.12.548736 |
Ejemplares similares
-
Efficient bi-allelic tagging in human induced pluripotent stem cells using CRISPR
por: Ren, Xingjie, et al.
Publicado: (2023) -
Base editing and prime editing in laboratory animals
por: Caso, Federico, et al.
Publicado: (2021) -
Prime Editing: An All-Rounder for Genome Editing
por: Lu, Chenyu, et al.
Publicado: (2022) -
Prime editing – an update on the field
por: Scholefield, Janine, et al.
Publicado: (2021) -
The risk variant rs11836367 contributes to breast cancer onset and metastasis by attenuating Wnt signaling via regulating NTN4 expression
por: Yang, Han, et al.
Publicado: (2022)