Searching journal content for articles similar to Verfaillie et al. 26 (7): 882.

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  1. ...reporter assays are high-throughput assays that quantify the activity of a test fragment, typically cloned downstream from a minimal promoter, via massively parallel sequencing of barcoded reporter transcripts.Multiplexing: A process in which multiple libraries are pooled and sequenced on the same lane...
  2. ...-occupancy TP53 enhancers, high levels of paused RNA polymerases, and accessible chromatin. Interestingly, two different shRNA screens failed to identify a single TP53 target gene required for the anti-proliferative effects of TP53 during pharmacological activation in vitro. Furthermore, bioinformatics analysis...
  3. ...in higher eukaryotes as well as their ability to respond and adapt to changing environmental conditions. While active TP53-recruiting cis-regulatory modules (CRMs) were shown to harbor an unsophisticated organization and very low complexity (Verfaillie et al. 2016), other studies have demonstrated...
  4. ...STARR trained on -wide enhancer activity data (de Almeida et al. 2022) and the BPNet model trained on endogenous TF binding and cooperativity (Avsec et al. 2021), suggesting that these rules are important in wild-type enhancer sequences. As an ectopic reporter assay STARR-seq measures the potential of sequences...
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