Precise genome editing using engineered nucleases can significantly facilitate biological studies and disease treatment. In particular, clustered regularly interspaced short palindromic repeats (CRISPR) with CRISPR-associated (Cas) proteins are a potentially powerful tool for modifying a genome by targeted cleavage of DNA sequences complementary to designed guide strand RNAs. Although CRISPR/Cas systems can have on-target cleavage rates close to the transfection rates, they may also have relatively high off-target cleavage at similar genomic sites that contain one or more base pair mismatches, and insertions or deletions relative to the guide strand. We have developed a bioinformatics-based tool, COSMID (CRISPR Off-target Sites with Mismatc...
CRISPR/Cas9 is a versatile genome-editing technology that is widely used for studying the functional...
The availability of genome sequences of numerous organisms and the revolution brought about by genom...
CRISPR-Cas9 is a powerful genome editing technology in which a single guide RNA (sgRNA) confers targ...
CRISPR genome editing has become a widely-used tool to easily and efficiently modify a genome of int...
© 2021, Springer Science+Business Media, LLC, part of Springer Nature.The CRISPR-Cas system facilita...
Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow for facile gen...
Motivation: Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow fo...
With ongoing development of the CRISPR/Cas programmable nuclease system, applications in the area of...
The Type II clustered regularly interspaced short palindromic repeats (CRISPR)/Cas system is an adap...
Although the CRISPR/Cas9/sgRNA system efficiently cleaves intracellular DNA at desired target sites,...
Although the CRISPR/Cas9/sgRNA system efficiently cleaves intracellular DNA at desired target sites,...
Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow for facile gen...
<div><p>Genome engineering has been revolutionized by the discovery of clustered regularly interspac...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, F...
Methods and systems for searching genomes for potential CRISPR off-target sites are provided. In pre...
CRISPR/Cas9 is a versatile genome-editing technology that is widely used for studying the functional...
The availability of genome sequences of numerous organisms and the revolution brought about by genom...
CRISPR-Cas9 is a powerful genome editing technology in which a single guide RNA (sgRNA) confers targ...
CRISPR genome editing has become a widely-used tool to easily and efficiently modify a genome of int...
© 2021, Springer Science+Business Media, LLC, part of Springer Nature.The CRISPR-Cas system facilita...
Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow for facile gen...
Motivation: Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow fo...
With ongoing development of the CRISPR/Cas programmable nuclease system, applications in the area of...
The Type II clustered regularly interspaced short palindromic repeats (CRISPR)/Cas system is an adap...
Although the CRISPR/Cas9/sgRNA system efficiently cleaves intracellular DNA at desired target sites,...
Although the CRISPR/Cas9/sgRNA system efficiently cleaves intracellular DNA at desired target sites,...
Clustered regularly interspaced short palindromic repeats (CRISPR) technologies allow for facile gen...
<div><p>Genome engineering has been revolutionized by the discovery of clustered regularly interspac...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, F...
Methods and systems for searching genomes for potential CRISPR off-target sites are provided. In pre...
CRISPR/Cas9 is a versatile genome-editing technology that is widely used for studying the functional...
The availability of genome sequences of numerous organisms and the revolution brought about by genom...
CRISPR-Cas9 is a powerful genome editing technology in which a single guide RNA (sgRNA) confers targ...