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Series GSE105002 Query DataSets for GSE105002
Status Public on Oct 16, 2018
Title High-fidelity base editing mediated by Cpf1-cytidine deaminase fusion
Organism Homo sapiens
Experiment type Other
Summary C-to-T base editing mediated by CRISPR/Cas9 base editors (BEs) needs a G/C-rich PAM and the editing fidelity is compromised by unwanted indels and non-C-to-T substitutions. We developed CRISPR/Cpf1-based BEs to recognize a T-rich PAM and induce efficient C-to-T editing with few indels and/or non-C-to-T substitutions. The requirement of editing fidelity in therapeutic-related trials necessitates the development of CRISPR/Cpf1-based BEs, which also facilitates base editing in A/T-rich regions.
 
Overall design Examination of indels and base substitutions induced by the CRISPR/Cpf1 base editors
 
Contributor(s) Yang L, Chen J, Huang X, Yang B, Wang Y, Li X
Citation(s) 29553573
Submission date Oct 16, 2017
Last update date Jul 25, 2021
Contact name Li Yang
E-mail(s) liyang_fudan@fudan.edu.cn
Organization name Fudan University
Department Institutes of Biological Sciences
Street address 131 Dong-An Road
City Shanghai
ZIP/Postal code 200032
Country China
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (40)
GSM2813782 Cpf1-BE0-2_1
GSM2813783 Cpf1-BE0-1_1
GSM2813784 Cpf1-BE0-1_4+Cpf1-BE0-2_1
Relations
BioProject PRJNA414402
SRA SRP119999

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE105002_Cpf1_Indels.xls.gz 19.3 Kb (ftp)(http) XLS
GSE105002_RAW.tar 13.5 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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