Searching journal content for articles similar to Takenaka and Matsuda 13 (6b): 1558.

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  1. ...Balancing Gene Ontology annotation specificity in protein function prediction 1 based on the protein sequence large graph 2 Jiangyi Shao1,2, Shutao Chen1, Ziwen Wang 1, Zixu Chen1,2, Bin Liu1,2* 3 1 School of Computer Science and Technology, Beijing Institute of Technology, 4 Beijing 100081, China...
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  2. ...and robustness against conventional machine learning techniques, including Gaussian mixture models (GMM-only), principal component analysis-based GMMs, k-means clustering, and hierarchical clustering. These validations, using an extensive and diverse array of data sets, including synthetic RNA constructs...
  3. ...in reconstructing spatial transcriptomic profiles in comparison with deconvolution-based approaches such as cell2location (Kleshchevnikov et al. 2022) and RCTD (Cable et al. 2022). Based on the high-resolution seqFISH+ data set, we simulated spatial spot data by aggregating gene expression profiles from neighboring...
  4. ...mutation cluster or hotspot (35% of cases; significance level of 5%). The majority of cases in which mutations were not clustered occurred in tumor-suppressor genes (TP53, PTEN, and VHL) (Supplemental Note 1; Supplemental Fig. 14), which acquire loss-of-function variants across a larger proportion of sites...
  5. ...joint profiling of copy number variation (CNV), RT, and gene expression from the same sample, providing a more accurate integrated view of the complex relationships between RT and gene regulation.Human cells duplicate their by the firing of thousands of origins that are activated in clusters following...
  6. ...clustering framework for spatial transcriptomics data that aggregates outcomes from state-of-the-art tools using a variety of consensus strategies, including Onehot-based, average-based, hypergraph-based, and wNMF-based methods. Comprehensive assessments on simulated and real data from distinct experimental...
  7. ....To further investigate the temporal specificity of drug effects, we first categorized genes from the input set into three temporal expression stages based on differential expression profiles: low (low vs. non-AD), intermediate (inter vs. non-AD and inter vs. low AD), and high (high vs. non-AD, high vs. low...
  8. ...epithelial-to-mesenchymal transition. Overall, ANS provides a robust and reliable gene signature scoring framework, significantly improving the accuracy of score-based annotation of cell types and states in single-cell studies.High-throughput single-cell RNA sequencing (scRNA-seq) is a powerful technology...
  9. ...) of cells from the Allen Brain Cell (ABC) Atlas (Yao et al. 2023) scRNA-seq data and snRNA-seq data from this study, colored by data set. SN, substantia nigra. (C) UMAP embedding and clustering analysis of snRNA-seq data (n = 40,125 nuclei) from this study, with cells colored based on cell classes...
  10. ...by the interplay of genes. Over the past decades, numerous computational methods have emerged to infer GRN from gene expression profiles. These include correlation-based networks (Chan et al. 2017; Specht and Li 2017), Gaussian graphical models (Kotiang and Eslami 2020), tree-based ensemble pipelines (Huynh-Thu et...
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