Searching journal content for articles similar to Feng et al. 34 (6): 822.

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  1. ..., and .False discovery rate control using Storey's q-valuesWe identify significant pathological shifts at the single-cell level by performing separate hypothesis testing for each cell. To control for false discoveries from multiple hypothesis testing, we apply the q-value method developed by Storey...
  2. ...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...
  3. ...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...
  4. ...). This method enabled us to pinpoint mRNA positions showing significant ASM (Fig. 3A). Among detected 14,609 and 13,542 candidate m6A sites in the replicate experiments, we identified 57 ASM sites (false discovery rate [FDR] < 0.1) with an average modification difference between the two alleles of 0.32.View...
  5. .... 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...
  6. .... This makes them insensitive in complex environments where the detailed dynamics of cell interactions matter. We introduce CellAgentChat, an agent-based model (ABM) designed to decipher CCIs from single-cell RNA sequencing and spatial transcriptomics data. This approach models biological systems...
  7. ...of adenosine (m6A) being the most common.View larger version: In this window In a new window Figure 1. Multiple RNA variables contribute to the production of distinct isoforms from the same gene. In alternative exon inclusion, an exon can be either included or spliced out of a transcript. In alternative TSS...
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  8. ...Sindri Emmanúel Antonsson and Páll Melsted Faculty of Industrial Engineering, Mechanical Engineering, and Computer Science, University of Iceland, 102 Reykjavík, Iceland Corresponding author: pmelsted@hi.isAbstractAs the number of experiments that employ single-cell RNA sequencing (scRNA-seq) grows...
  9. ...of intermediate fibers that typically transition to a pure fast or slow fiber with exercise training (Klitgaard et al. 1990; Williamson et al. 2001; Harber and Trappe 2008). ATAC-seq data are distributed differently than RNA-seq data, and loci are more abundant, making DARs more sensitive to false-discovery rate...
  10. ...: padamopoulos@biol.uoa.grAbstractEpitranscriptomics, a rapidly evolving field mainly driven by massive parallel sequencing technologies, explores post-transcriptional RNA modifications. N6-methyladenosine (m6A) has emerged as the most prominent and dynamically regulated modification in human mRNAs, being...
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