Searching journal content for articles similar to Liu et al. 31 (9): 1573.

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  1. ...421 developmental transitions and lineage specification 422 To identify the main TFs associated with chromatin accessibility dynamics in 423 candidate CREs regulated during embryogenesis, TFBM enrichment was 424 conducted for all DARs associated with promoters and putative enhancers. 425 Significant...
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  2. ...), consistent with the essential role of these TFs in five out of the six conditions in developmental processes. Imbalanced peaks are also slightly less conserved (Supplemental Fig. S3G).Overall, our results demonstrate that genetic variation has an extensive impact on TF occupancy during embryogenesis in vivo...
  3. ...of C. elegans cohesin is about 10-fold shorter, and the binding of NIPBL ortholog does not depend on cohesin. We propose that preferential loading and loop extrusion by cohesin is an evolutionarily conserved mechanism that regulates the 3D interactions of enhancers in animal s.In mammalian s, cohesin...
  4. ...and conditionsTo identify robust biological signals that characterize conserved cellular programs, we can naturally extend geneCover to enable marker gene selection across multiple samples and conditions. In this generalized formulation, we require every gene in the transcriptome G to be covered by at least one...
  5. ...contribution of the epi to selective enhancer activation by ESR1 remains to be fully elucidated. To address this, we employ a massively parallel reporter assay to profile 7576 individual ESR1 binding sites for hormone responsiveness. Only a minority of ESR1-occupied enhancers exhibit hormone-induced activity...
  6. ...BP GO term enrichment of genes adjacent to CrxK88N-reduced ATAC-seq peaks.CrxK88N-increased accessibility CREs show progenitor cell regulatory signatures and are developmentally silenced during photoreceptor differentiationLast, we sought to understand the functional significance of CRXK88N...
  7. ...to postnatal stages, and pinpointing critical trait-affecting enhancers remains largely unaddressed. In the present study, we aim to fill this gap by identifying potential critical enhancers and their gene regulatory networks during PSM development.Our approach involves analyzing developmental trajectories...
  8. ....35) with Williams–Beuren syndrome DDT (WSD) or D-TOX E motif. The conserved GxD signature is highlighted with a red bar. (Q) Query (ICOPa), (ss_pred) secondary structure prediction, and (T) template. For a more detailed output format description, please consult https://toolkit.tuebingen.mpg.de/tools/hhpred. (B...
  9. ...al. 2013; Werner et al. 2017), demonstrating a genetic basis, and possible selection, for mouth-form ratios in the wild.View larger version: In this window In a new window Figure 1. Developmental transcriptomics of mouth-form plasticity in Pristionchus pacificus. (A) The two mouth forms developed...
  10. ...the original reference data to 50% and evaluated the accuracy of both CAMUS and random sampling. The performance of CAMUS still significantly outperforms random selection (Supplemental Fig. S1D). This implies that reference data selection can enhance annotation accuracy and rare cell type identification...
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