Searching journal content for articles similar to Owen et al. 13 (8): 1828.

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  1. ...embeddings for downstream machine-learning tasks. Much less has been done to examine the embeddings directly, especially analyses of gene sets in embedding spaces. Here, we propose an Algorithm for Network Data Embedding and Similarity (ANDES), a novel best-match approach that can be used with existing gene...
  2. ...clusters within the . Using the algorithm described in the Methods section, we identified 18 spatial clusters of genes in which the sum of the genes’ log ratios was significantly larger than would be expected by chance on a -wide basis (Supplemental Data S2; up-regulated and down-regulated clusters...
  3. ...of coexpressed gene neighbors in C. briggsae and asked whether the C. elegans orthologs are also coexpressed. We found that the general level of expression similarity was dramatically lower, despite examining only C. elegans orthologs within conserved gene neighborhoods (Fig. 4A). We next examined those C...
  4. ..., Srf, and Sp1 from a set of human-muscle-specific genes. It also discovered the NFAT motif from genes up-regulated by CD28 stimulation in T-cells, which implies the direct involvement of NFAT in mediating the CD28 stimulatory signal. Using Caenorhabditis elegans – Caenorhabditis briggsae comparison...
  5. ...to external stress in an expanding list of eukaryotes: It is involved in mitochondrial stress adaptation in the worm Caenorhabditis elegans (Ma et al. 2019), the expression of neuronal genes in the fly Drosophila melanogaster (Yao et al. 2018), salt and temperature tolerance in the rice Oryza sativa (Zhang et...
  6. ...of thousands of short open reading frames (sORFs; <100 codons) whose coding potential has been the subject of recent reviews (Andrews and Rothnagel 2014; Couso 2015; Hellens et al. 2016; Couso and Patraquim 2017; Rothnagel and Menschaert 2018; Ruiz-Orera and Albà 2019). However, gene annotation algorithms...
  7. ...ones. For selected human and mouse candidate pairs, qRT-PCR and in vitro RNA structure probing supported both shared expression and shared structure despite low abundance and low sequence identity. About 30,000 CRS regions are located near coding or long noncoding RNA genes or within enhancers...
  8. ...a transmembrane (TM) domain by the TMHMM algorithm is shown ( Krogh et al. 2001 ). Step (5): Pairwise relationships among PDZ domain-encoding genes and the PDZCBM gene set are determined from correlated mRNA levels, cellular localization, and common literature co-citation patterns between a PDZ gene and potential...
  9. ...( HD ) from LAGAN ( top four sequence tracks) and ClustalW ( bottom four sequence tracks). The sequence tracks in order are (1) mouse, (2) rat, (3) human, (4) Fugu, (5) mouse, (6) rat, (7) human, and (8) Fugu. For the LAGAN algorithm, the start of translation of the HD gene in each species aligns...
  10. ...clustering algorithms and data visualization tools to allow for analysis and presentation of the large volume of microarray results. An early approach, which is still probably one of the most popular, is the application of hierarchical clustering to group similarly expressed genes together, representing...
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