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Open AccessJournal ArticleDOI

Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system.

TLDR
In this paper, the authors characterized Cpf1, a putative class 2 CRISPR effector, which is a single RNA-guided endonuclease lacking tracrRNA and utilizes a T-rich protospacer-adjacent motif.
About
This article is published in Cell.The article was published on 2015-10-22 and is currently open access. It has received 3436 citations till now. The article focuses on the topics: CRISPR/Cpf1 & Cas9.

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Citations
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Journal ArticleDOI

Non-viral delivery systems for CRISPR/Cas9-based genome editing: Challenges and opportunities

TL;DR: The pros and cons of delivering CRISPR/Cas9 systems in the form of plasmid, mRNA, or protein are analyzed and promising strategies to overcome barriers are proposed.
Journal ArticleDOI

History of CRISPR-Cas from Encounter with a Mysterious Repeated Sequence to Genome Editing Technology.

TL;DR: The fascinating history of CRISPR-Cas systems is discussed, from the original observation of an enigmatic sequence in E. coli to genome editing in humans and providing insights into the origin and evolution of this system from mobile genetic elements denoted casposons.
Posted ContentDOI

Protocol: Genome-scale CRISPR-Cas9 Knockout and Transcriptional Activation Screening

TL;DR: A protocol for genome-scale knockout and transcriptional activation screening using the CRISPR-Cas9 system is described to validate candidate genes identified from the screen and strategies for confirming the screening phenotype as well as genetic perturbation are described.
Journal ArticleDOI

Applying CRISPR/Cas for genome engineering in plants: the best is yet to come

TL;DR: It will be desirable to apply the CRISPR/Cas nuclease system for the mutation of regulatory elements and for more complex genome rearrangements, like transcriptional regulators or DNA modifying enzymes, in the future.
Journal ArticleDOI

Multiplexed CRISPR technologies for gene editing and transcriptional regulation.

TL;DR: This review discusses multiplexed CRISPR technologies and describes methods for the assembly, expression and processing of synthetic guide RNA arrays in vivo, and offers a glimpse of emerging challenges and emphasize experimental considerations for future studies.
References
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Journal ArticleDOI

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.

TL;DR: A new criterion for triggering the extension of word hits, combined with a new heuristic for generating gapped alignments, yields a gapped BLAST program that runs at approximately three times the speed of the original.
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Fast and accurate short read alignment with Burrows–Wheeler transform

TL;DR: Burrows-Wheeler Alignment tool (BWA) is implemented, a new read alignment package that is based on backward search with Burrows–Wheeler Transform (BWT), to efficiently align short sequencing reads against a large reference sequence such as the human genome, allowing mismatches and gaps.
Journal ArticleDOI

MUSCLE: multiple sequence alignment with high accuracy and high throughput

TL;DR: MUSCLE is a new computer program for creating multiple alignments of protein sequences that includes fast distance estimation using kmer counting, progressive alignment using a new profile function the authors call the log-expectation score, and refinement using tree-dependent restricted partitioning.
Journal ArticleDOI

A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.

TL;DR: This study reveals a family of endonucleases that use dual-RNAs for site-specific DNA cleavage and highlights the potential to exploit the system for RNA-programmable genome editing.
Journal ArticleDOI

Multiplex Genome Engineering Using CRISPR/Cas Systems

TL;DR: The type II prokaryotic CRISPR (clustered regularly interspaced short palindromic repeats)/Cas adaptive immune system has been shown to facilitate RNA-guided site-specific DNA cleavage as discussed by the authors.
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