Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing

Cytidine base editors are powerful tools for making subtle genome alterations. Here the authors analyse edited human iPSCs with whole genome sequencing and reveal the spectrum of off-target effects.

Bibliographic Details
Main Authors: Erica McGrath, Hyunsu Shin, Linyi Zhang, Je-Nie Phue, Wells W. Wu, Rong-Fong Shen, Yoon-Young Jang, Javier Revollo, Zhaohui Ye
Format: Article
Language:English
Published: Nature Publishing Group 2019-11-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-019-13342-8
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spelling doaj-af712862da014df4afe9e07f5f556c662021-05-11T11:38:04ZengNature Publishing GroupNature Communications2041-17232019-11-011011910.1038/s41467-019-13342-8Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencingErica McGrath0Hyunsu Shin1Linyi Zhang2Je-Nie Phue3Wells W. Wu4Rong-Fong Shen5Yoon-Young Jang6Javier Revollo7Zhaohui Ye8Division of Cellular and Gene Therapies, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug AdministrationDivision of Cellular and Gene Therapies, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug AdministrationDivision of Cellular and Gene Therapies, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug AdministrationFacility for Biotechnology Resources, Center for Biologics Evaluation and Research, Food and Drug AdministrationFacility for Biotechnology Resources, Center for Biologics Evaluation and Research, Food and Drug AdministrationFacility for Biotechnology Resources, Center for Biologics Evaluation and Research, Food and Drug AdministrationDepartment of Oncology, Johns Hopkins School of MedicineDivision of Genetic and Molecular Toxicology, National Center for Toxicology Research, Food and Drug AdministrationDivision of Cellular and Gene Therapies, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug AdministrationCytidine base editors are powerful tools for making subtle genome alterations. Here the authors analyse edited human iPSCs with whole genome sequencing and reveal the spectrum of off-target effects.https://doi.org/10.1038/s41467-019-13342-8
collection DOAJ
language English
format Article
sources DOAJ
author Erica McGrath
Hyunsu Shin
Linyi Zhang
Je-Nie Phue
Wells W. Wu
Rong-Fong Shen
Yoon-Young Jang
Javier Revollo
Zhaohui Ye
spellingShingle Erica McGrath
Hyunsu Shin
Linyi Zhang
Je-Nie Phue
Wells W. Wu
Rong-Fong Shen
Yoon-Young Jang
Javier Revollo
Zhaohui Ye
Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
Nature Communications
author_facet Erica McGrath
Hyunsu Shin
Linyi Zhang
Je-Nie Phue
Wells W. Wu
Rong-Fong Shen
Yoon-Young Jang
Javier Revollo
Zhaohui Ye
author_sort Erica McGrath
title Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
title_short Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
title_full Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
title_fullStr Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
title_full_unstemmed Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
title_sort targeting specificity of apobec-based cytosine base editor in human ipscs determined by whole genome sequencing
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2019-11-01
description Cytidine base editors are powerful tools for making subtle genome alterations. Here the authors analyse edited human iPSCs with whole genome sequencing and reveal the spectrum of off-target effects.
url https://doi.org/10.1038/s41467-019-13342-8
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