Searching journal content for articles similar to Heyer et al. 9 (11): 1106.

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  1. ...a filter of a minimum of 1% of the cells of the data set which had to have robust expression for both the host and the nested gene, selecting 34 pairs. Finally, expression above the threshold for both the host and the nested gene allows the identification of cells which coexpress the pair. Expression above...
  2. ...-read fusion identificationIn exploring the fusion isoforms identified by CTAT-LR-Fusion using combined long and short reads we found 213 fusion genes with 288 fusion splicing isoforms having both short- and long-read alignments together supporting each of the fusion transcript breakpoints. Fusion expression...
  3. ...it to sequencing data from an in vitro infection time course using VeroE6 cells that were either WT, overexpressing ACE2, or overexpressing ACE2 and TMPRSS2 (Hoffmann et al. 2020). ACE2 and TMPRSS2 coexpressing cells have the most obviously altered sgRNA kinetics, with the peak level of sgRNA occurring at 48 h...
  4. ...’s effectiveness through three case studies on transcription factor activity prediction, 29 early haematopoiesis, and tumour microenvironments. Provided as an R package, NNet offers 30 a novel framework for exploring cellular variation in coexpression and integrates seamlessly 31 with existing single-cell analysis...
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  5. ...for further experimental studies to understand and therapeutically target the links between cell shape, cell signaling, and gene regulation in the context of breast cancer.MethodsWGCNA analysisUsing weighted correlation network analysis, we performed coexpression module identification using the R package...
  6. ...-capture-imputed networks. (E) Enrichment of the cluster subnetworks in TF PPIs (TF networks), for pre-capture (PRE) and imputed (POST) networks. The circle sizes show the number of genes in each TF PPI term.TF capture facilitates the identification of TFs associated with developmental trajectoriesTo explore...
  7. ...other germ layers, for example, brain (ectoderm) or heart ventricle, adrenal, or kidney (mesoderm) (Supplemental Fig. S3). However, strong coexpression was not observed in any single tissue type. To explore this further, we integrated the human embryonic data with RNA-seq from differentiating human...
  8. ...and sequencebased alignments (Managadze et al. 2011) have indicated that RNA secondary structures are depleted in lncRNAs (Ulitsky and Bartel 2013). The low sequence conservation of most lncRNAs, while complicating identification of CRSs, does not preclude their existence, such as in telomerase RNA (structurally...
  9. ...for the identification of AS events such as exon skipping or intron retention and have established the involvement of AS in many biological processes. However, both technologies have serious limitations for the reconstruction of the actual expressed transcripts, as short reads break the continuity of the transcript...
  10. ...coexpression modules with differential responses to environmental microbiota. Third, we link the microbial and host transcriptome data by predicting a global map of more than 2800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential...
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