Searching journal content for articles similar to Rouillard et al. 11 (8): 1453.

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  1. ...in this window to the enhancer. More restrictive enhancer-607 gene assignments were made by sorting genes into activity classes based on expression in the 608 RNA-seq data (expression threshold: TPM > 1). For each activity class, genes were matched to 609 the allowed set of enhancers by scanning 15 kb upstream...
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  2. ...), with names for selected genes. (Bottom) Virtual 4C track (see Methods) showing Hi-C contacts from MYC toward the Chromosome 10 region for 10A (blue), T1 (yellow), and C1 (green). (E) FISH image of the MYC gene (yellow) and the Chromosome 10 enhancer (blue; Chr 10 position 73,117,711–73,267,436) expected...
  3. ...(Browne et al. 2002; Goyal et al. 2005; Banton and Tunnacliffe 2012). However, the absence of high-quality, chromosome-level assemblies has thus far restricted more detailed investigations into the underlying regulatory mechanisms. In recent years, more haplotype s have been analyzed which provide...
  4. ...-seq assemblers (Fig. 4). Globally, TOGA achieved greater reference protein coverage than Liftoff, and in vertebrates, TOGA achieved the highest reference protein coverage (H. sapiens) or was virtually tied with BRAKER3 (G. gallus) (Fig. 4). In vertebrates, the RNA-seq assemblers obtained slightly lower reference...
  5. ...contributed equally to this work. Corresponding authors: thomas.near@yale.edu, clad@ihb.ac.cn, yangliandong1987@163.comAbstractGenomic evolution can propel and restrict species diversification. Rapid molecular evolution and genomic rearrangement is often associated with increased species diversification...
  6. ...on microscopic chromosome examination, a complex and expertise-dependent process with megabase-scale resolution. Optical mapping (OGM) technology offers an efficient approach to detect large-scale genomic lesions. Here, we introduce OMKar, a computational method that generates virtual karyotypes from OGM data...
  7. ...: chirag@iisc.ac.inAbstractAffordable genotyping methods are essential in genomics. Commonly used genotyping methods primarily support single-nucleotide variants and short indels but neglect structural variants. Additionally, accuracy of read alignments to a reference is unreliable in highly polymorphic...
  8. ...: jinulee@yonsei.ac.kr (J.L.) 26 27 Abstract 28 Homology-directed repair (HDR) enables precise editing; however, its 29 application in mammalian cells is limited by low efficiency due to competition from error-30 prone repair pathways and intrinsically restricted HDR activity. Existing HDR-31 enhancement...
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  9. ...for Genome Sciences and Systems Biology, Washington University School of Medicine in St. Louis, St. Louis, Missouri 63110, USA; 3Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine in St. Louis, St. Louis, Missouri 63110, USA; 4Center for Biomolecular Condensates...
  10. .... 2001; The ENCODE Project Consortium 2004; McGarvey et al. 2015; Frankish et al. 2019). These reference annotations are absolutely essential for virtually all transcriptomics research and beyond, but they lack information on what tissues and cell types express what isoforms and at what level.A resource...
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