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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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Citations
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CRISPR/Cas9 cleavage efficiency regression through boosting algorithms and Markov sequence profiling.

TL;DR: A two-step averaging method for the regression of cleavage efficiencies of a set of sgRNAs by averaging the predicted efficiency scores of a boosting algorithm and those by a support vector machine (SVM) and it is proposed to use profiled Markov properties as novel features to capture the global characteristics of sGRNAs.
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Mechanisms of Long Non-Coding RNAs in the Assembly and Plasticity of Neural Circuitry.

TL;DR: This review summarized latest advances concerning roles and mechanisms of lncRNAs in assembly, maintenance and plasticity of neural circuitry, as well as lnc RNAs' implications in neurological disorders.
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High-Throughput Silencing Using the CRISPR-Cas9 System: A Review of the Benefits and Challenges.

TL;DR: It is envisaged that complementarities between CRISPR, siRNA, and shRNA will ensure that all three technologies remain critical to the success of future functional genomics projects.
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An inducible CRISPR-ON system for controllable gene activation in human pluripotent stem cells.

TL;DR: A CRISPR-ON system to efficiently upregulate endogenous genes in hPSCs and shows that the dCas9-VPR level could be precisely and reversibly controlled by the addition and withdrawal of Dox, and an elevated NANOG level promoted naïve pluripotent gene expression, enhanced cell survival and clonogenicity.
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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