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Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex

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The article was published on 2016-05-22 and is currently open access. It has received 1792 citations till now. The article focuses on the topics: CRISPR.

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The Past, Present, and Future of Genetic Manipulation in Toxoplasma gondii

TL;DR: The major strategies for T. gondii genetic manipulation including genetic crosses, insertional mutagenesis, chemical mutagenisation, homologous gene replacement, conditional knockdown techniques, and the recently developed clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system are summarized.
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On-chip multiplexed single-cell patterning and controllable intracellular delivery

TL;DR: A vacuum-assisted micropore array platform that enables massively parallel single-cell manipulation and the intracellular delivery of macromolecules and small molecules and provides a simple, efficient, high-throughput intrACEllular delivery method that may facilitate on-chip cell manipulation, intrace cellular investigation and cancer therapy.
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RNA-guided retargeting of Sleeping Beauty transposition in human cells

TL;DR: This work demonstrates biased genome-wide integration of the Sleeping Beauty (SB) transposon by combining it with components of the CRISPR/Cas9 system and provides proof-of-concept that it is possible to influence the target site selection of SB by fusing it to a catalytically inactive Cas9 and by providing a single guide RNA against the human Alu retrotransposon.
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Myoediting: Toward prevention of muscular dystrophy by therapeutic genome editing

TL;DR: A historical overview of genome-editing technologies is provided, the most recent advances are summarized, and potential strategies and challenges for permanently correcting genetic mutations that cause muscular dystrophies are discussed.
References
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Fast gapped-read alignment with Bowtie 2

TL;DR: Bowtie 2 combines the strengths of the full-text minute index with the flexibility and speed of hardware-accelerated dynamic programming algorithms to achieve a combination of high speed, sensitivity and accuracy.
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RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome

TL;DR: It is shown that accurate gene-level abundance estimates are best obtained with large numbers of short single-end reads, and estimates of the relative frequencies of isoforms within single genes may be improved through the use of paired- end reads, depending on the number of possible splice forms for each gene.
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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.
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The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity

TL;DR: The results indicate that large, annotated cell-line collections may help to enable preclinical stratification schemata for anticancer agents and the generation of genetic predictions of drug response in the preclinical setting and their incorporation into cancer clinical trial design could speed the emergence of ‘personalized’ therapeutic regimens.
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Molecular signatures database (MSigDB) 3.0

TL;DR: A new version of the database, MSigDB 3.0, is reported, with over 6700 gene sets, a complete revision of the collection of canonical pathways and experimental signatures from publications, enhanced annotations and upgrades to the web site.
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