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Application of CRISPR/Cas9 Pooled Screening for a Non-immediate Readout Model
Date
2024-01-01
Author
Terzi Çizmecioğlu, Nihal
Metadata
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Linking phenotypes to genetic components has been an essential part of novel drug discovery, and screening methods have been widely employed to achieve such a goal. Screens can be conducted in either pooled or arrayed formats. Although arrayed screenings provide a better and cheaper alternative in small scale, the larger-scale screenings are conducted in pooled manner. With its adaptability to various models and conditions, CRISPR/Cas9 technology provides an invaluable alternative to classical and RNAi-based screening methods. Combined with high-throughput sequencing and bioinformatics, CRISPR-/Cas9-based pooled screening methods provide unbiased and robust data. In this protocol, we employed CRISPR-/Cas9-based pooled screening for a non-binary and non-immediate readout.
Subject Keywords
Cas9
,
CRISPR
,
Differentiation
,
Neuroectoderm
,
Pooled screening
,
Sox1GFP
URI
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85199224188&origin=inward
https://hdl.handle.net/11511/110736
Journal
Methods in molecular biology (Clifton, N.J.)
DOI
https://doi.org/10.1007/7651_2024_529
Collections
Department of Biology, Article
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BibTeX
N. Terzi Çizmecioğlu, “Application of CRISPR/Cas9 Pooled Screening for a Non-immediate Readout Model,”
Methods in molecular biology (Clifton, N.J.)
, vol. 2849, pp. 87–116, 2024, Accessed: 00, 2024. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85199224188&origin=inward.