Searching journal content for articles similar to Deng et al. 33 (10): 1690.

Displaying results 1-10 of 5866
For checked items
  1. ...the significance of cellular state deviations from a healthy reference, we introduce single-cell Pathological Shift Scoring (scPSS). scPSS uses gene expression profiles from normal cells to establish a reference state distribution, using k-nearest neighbor distances in principal component embedding space. For any...
  2. ...expression profiles were obtained for individual cells after standard quality control and filtering.To mimic lower-resolution spatial transcriptomic platforms, we simulated 189 spatial pseudospots by aggregating transcriptomes of spatially adjacent single cells. For each pseudospot, the aggregated expression...
  3. ..._expr but not in the recent_expr data set (Supplemental Fig. S25; Supplemental Table S10). This was also coherent with dendrogram analyses of DE genes (Supplemental Fig. S26).Altogether, whole-transcriptome patterns, gene modules, and differential expressed genes detected by both methods show more convergent evolution...
  4. ...and target genes (Gao et al. 2023).Single-cell RNA sequencing (scRNA-seq) enables gene expression profiling at the individual cell level, revealing cellular heterogeneity with single-cell resolution and significantly enhancing the understanding of cell type–specific gene regulation (Chen and Liu 2022; Kartha...
  5. ...a systematic comparison between single-cell long-read and conventional short-read RNA sequencing techniques. The transcriptome of approximately 30,000 mouse retina cells was profiled using 1.54 billion Illumina short reads and 1.40 billion Oxford Nanopore Technologies long reads. Consequently, we identify 44...
  6. ...intestine, spleen, and thymus, and three different data modalities, which include single-cell RNA-seq (scRNA-seq), single-cell ATAC-seq (scATAC-seq), and spatial transcriptomics (Slide-seq). Figure 1, A through C, presents an overview of GIANT. We first construct gene graphs for cell clusters from each...
  7. ...signatures from rare sources of variability. To facilitate the discovery of genes associated with all sources of transcriptomic variability, we introduce geneCover, a label-free correlation-based marker gene selection method designed for single-cell RNA sequencing and spatial transcriptomics data. gene...
  8. ...; Jensen et al. 2020; Hokken et al. 2021; Egan and Sharples 2023). Insight into the coordinated transcriptomic and epigenomic molecular responses to exercise within each of the diverse muscle cell types is lacking; single-cell (sc) assays enable the characterization of the exercise response within...
  9. ...changes in firing patterns with decreased spike number over multiple developmental time points (Fig. 5B; Supplemental Fig. S6C). Notably, although control neurons show anticipated increases in spiking with maturity, depletion of nearly every transcriptional regulator dampened or fully blocked...
  10. .... Recent advancements in single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics (ST) technologies have empowered the comprehensive characterization of gene programs at both single-cell and spatial resolutions. Here, we present DeCEP, a computational framework designed to characterize context...
For checked items

Preprint Server