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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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Identification of LncRNA Linc00513 Containing Lupus-Associated Genetic Variants as a Novel Regulator of Interferon Signaling Pathway.

TL;DR: The data identify two functional promoter variants of linc00513 that contribute to increased level of l inc00513 and confer susceptibility on SLE and extends the role of lncRNAs in the pathogenesis of SLE.
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Drug-tunable multidimensional synthetic gene control using inducible degron-tagged dCas9 effectors.

TL;DR: A toolkit of conditionally degradable or stabilisable orthologous dCas9 or Cpf1 effector proteins is generated, opening options for multidimensional control of functional activities through combinations of orthogonal, drug-tunable artificial transcription factors.
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SWISS: multiplexed orthogonal genome editing in plants with a Cas9 nickase and engineered CRISPR RNA scaffolds

TL;DR: A CRISPR simultaneous and wide-editing induced by a single system (SWISS), in which RNA aptamers engineered in crRNA scaffold recruit their cognate binding proteins fused with cytidine deaminases and adenosine deaminase to Cas9 nickase target sites to generate multiplexed base editing.
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Modulating the expression of long non‐coding RNAs for functional studies

TL;DR: A collection of different methods used to modulate lncRNA expression levels for the assessment of biological function are surveyed, from RNA‐targeted strategies, genetic deletions, to engineered gene regulatory systems.
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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