Searching journal content for articles similar to Mogno et al. 23 (11): 1908.

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  1. ...RNA Center of Excellence, Sanofi Pasteur Inc., Waltham, MA, USA. ♱Corresponding authors: izg5139@psu.edu, nadav.ahituv@ucsf.edu Abstract Massively parallel reporter assays (MPRAs) represent a set of high-throughput technologies that measure the functional effects of thousands of sequences/variants on gene...
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  2. ...the reference, such as disease- and trait-associated variants or engineered sequences. Recent work has applied synthetic regulatory genomics to characterized dozens of deletions, inversions, and rearrangements of DNase I hypersensitive sites (DHSs). Here, we use the state-of-the-art model Enformer to predict...
  3. ..., Cohen BA. 2013. Massively parallel synthetic promoter assays reveal the in vivo effects of binding site variants. Genome Res 23: 1908–1915. doi:10.1101/gr.157891.113 ↵Mullokandov G, Baccarini A, Ruzo A, Jayaprakash AD, Tung N, Israelow B, Evans MJ, Sachidanandam R, Brown BD. 2012. High...
  4. ...Institute for Precision Medicine, University of Washington, Seattle, Washington 98195, USA Corresponding authors: rmyers@hudsonalpha.org, gcooper@hudsonalpha.orgAbstractMassively parallel reporter assays (MPRAs) are useful tools to characterize regulatory elements in human s. An aspect of MPRAs...
  5. ...Identification of determinants of differential chromatin accessibility through a massively parallel -integrated reporter assay Jennifer Hammelman1,2, Konstantin Krismer2,3, Budhaditya Banerjee4, David K. Gifford2,3,5 and Richard I. Sherwood4,6 1Computational and Systems Biology, Massachusetts...
  6. ...-seq), like other episomal massively parallel reporter assays (MPRAs) (Melnikov et al. 2012; Patwardhan et al. 2012), directly quantifies enhancer activity by relying on transcription factors within a host cell system, thereby removing any chromatin-associated biases (Arnold et al. 2013). STARR-seq takes...
  7. ...expression of the sequences of more than 25,000 RNA-binding protein (RBP) binding sites in primary mouse T cells using a massively parallel reporter assay. GC-rich sequences were destabilizing of reporter mRNAs and come from more rapidly evolving regions of the . These sequences were more likely to be folded...
  8. ...-regulatory function by deploying massively parallel reporter assays (MPRAs) in mouse retina explants carrying knock-ins of two variants, one in the DNA-binding domain (p.R90W) and the other in the transcriptional effector domain (p.E168d2). The degree of reporter gene dysregulation in these mutant Crx retinas...
  9. ...assays (Nord et al. 2013; Visel et al. 2013), never before has massively parallel cis-regulatory analysis been conducted in the mammalian CNS in vivo. Here, we sought to overcome current technological hurdles by developing a “capture-and-clone” approach for synthesizing CRE-seq libraries...
  10. ...elements by synthetic saturation mutagenesis. Nat Biotechnol 27: 1173–1175. ↵Patwardhan RP, Hiatt JB, Witten DM, Kim MJ, Smith RP, May D, Lee C, Andrie JM, Lee SI, Cooper GM, et al. 2012. Massively parallel functional dissection of mammalian enhancers in vivo. Nat...
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