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CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology.

Authors :
Wu WH
Tsai YT
Justus S
Cho GY
Sengillo JD
Xu Y
Cabral T
Lin CS
Bassuk AG
Mahajan VB
Tsang SH
Source :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2018; Vol. 1715, pp. 191-205.
Publication Year :
2018

Abstract

CRISPR/Cas9 genome engineering is currently the leading genome surgery technology in most genetics laboratories. Combined with other complementary techniques, it serves as a powerful tool for uncovering genotype-phenotype correlations. Here, we describe a simplified protocol that was used in our publication, CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa, providing an overview of each section of the experimental process.

Details

Language :
English
ISSN :
1940-6029
Volume :
1715
Database :
MEDLINE
Journal :
Methods in molecular biology (Clifton, N.J.)
Publication Type :
Academic Journal
Accession number :
29188514
Full Text :
https://doi.org/10.1007/978-1-4939-7522-8_13