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  1. ...'s Hospital, Boston, MA 02115, USA Corresponding author: dongwon.lee@childrens.harvard.eduAbstractMassively parallel reporter assays (MPRAs) are a high-throughput method for evaluating in vitro activities of thousands of candidate cis-regulatory elements (CREs). In these assays, candidate sequences are cloned...
  2. ...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...
  3. ...development of multiomicmethods provided tools for the assessment of cell identity and cell-to-cell heterogeneity. Multiomic, single-cell methods also inform on distinct aspects of the epi in parallel with gene expression (Cao et al. 2018; Zhu et al. 2019; Flynn et al. 2023). Approaches that map features of 3...
  4. ...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...
  5. ...monomeric and dimeric CRX binding sites promote distinct levels of transcriptional activation is not known.Recently, massively parallel reporter assays (MPRAs) have emerged as powerful tools for quantifying the regulatory activity of many CREs simultaneously. These assays work by introducing libraries...
  6. ...-throughput methods such as massively parallel splicing assay (MaPSy) (Soemedi et al. 2017), variant exon sequencing (Vex-seq) (Adamson et al. 2018), and multiplexed functional assay of splicing using Sort-seq (MFASS) (Chong et al. 2019), the SeqSplice method measured variant effect on a single exon but presented...
  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. ...(Zamir et al. 2022; Ruggeri et al. 2002), autoimmune diseases (Li et al. 2022) and cancer (Purdy and Campbell 2009; Naranbhai et al. 2021). Because of the importance of these polymorphic genes, researchers created the Immuno Polymorphism Database (IPD) to curate the HLA and KIR allele sequences (IPD...
  9. ...in functionally interpreting these data. To address this issue, massively parallel reporter assays (MPRAs) have emerged, in which barcoded reporter libraries are introduced into cells, and the resulting barcoded transcripts are quantified by next-generation sequencing. Thus far, MPRAs have been largely restricted...
  10. ...), and the regulatory activity of more than one million unique DNA fragments can now be assayed in a single experiment using such massively parallel reporter assays (Arnold et al. 2013).Here, we have developed a novel high-throughput approach to efficiently measure the activity of regulatory elements captured from...
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