Accounting for diversity in the design of CRISPR-based therapeutic genome editing

CRISPR cell and gene therapy have been designed largely with respect to a single reference human genome. A new study reveals how human genetic diversity could lead to off-target effects and presents a new tool to identify these risks.

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Veröffentlicht in:Nature genetics 2023-01, Vol.55 (1), p.6-7
1. Verfasser: Saha, Krishanu
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description CRISPR cell and gene therapy have been designed largely with respect to a single reference human genome. A new study reveals how human genetic diversity could lead to off-target effects and presents a new tool to identify these risks.
doi_str_mv 10.1038/s41588-022-01272-z
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subjects 45/41
631/1647
631/61/201
Agriculture
Animal Genetics and Genomics
Biomedical and Life Sciences
Biomedicine
Blood diseases
Cancer Research
Cancer therapies
CRISPR
CRISPR-Cas Systems - genetics
Drug development
Editing
Editors
Gene Editing
Gene Function
Gene therapy
Genetic diversity
Genomes
Human Genetics
Medical research
News & Views
news-and-views
Nucleotide sequence
Patients
Polymorphism
Product design
Product safety
Product testing
Sickle cell disease
title Accounting for diversity in the design of CRISPR-based therapeutic genome editing
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