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  1. ...with particular reference to the “innovation–amplification–divergence” model of neofunctionalization (Näsvall et al. 2012), in which a pre-existing, weak, secondary gene function (“innovation”) confers advantage owing to changes in the environment, leading to selection for increased gene copy (“amplification...
  2. ...change and dispersion for RNA-seq data with DESeq2. Genome Biol 15: 550. doi:10.1186/s13059-014-0550-8 ↵Maniatis T, Kee SG, Efstratiadis A, Kafatos FC. 1976. Amplification and characterization of a beta-globin gene synthesized in vitro. Cell 8: 163–182. doi:10.1016/0092-8674(76)90001-5 ↵Marco A. 2018...
  3. ...DRS and PCS to study clear cell renal cell carcinoma (ccRCC), focusing on new transcript and gene discovery. Twelve primary ccRCC archival tumors, six from patients who went on to relapse, were analyzed. Results were validated in an independent cohort of 20 patients by qRT-PCR and compared to DRS...
  4. .... More specialized tools for this approach include the Peak Browser at ChIP Atlas (Oki et al. 2018) or browsing ChIPBase (Huang et al. 2023), which is especially strong for ncRNAs but can also be used for mRNA genes. The Eukaryotic Promoter Database ExPASy has the useful Mass Genome Annotation Archive...
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  5. .... PARTAGE allowed us to simultaneously map CNV, RT, and gene expression from the same sample (Fig. 3B). First, whole- sequencing of the cell populations isolated from G1 enabled the accurate mapping of CNV and the detection of multiple amplifications in the HepG2 (Fig. 3B). Next, RT was mapped using...
  6. ...with the tumor microenvironment. We propose Smart-3SEQ as a highly cost-effective method to enable large gene expression profiling experiments unconstrained by sample size and tissue availability. In particular, Smart-3SEQ's compatibility with FFPE tissue unlocks an enormous number of archived clinical samples...
  7. ...-GRN was further validated by its strong performance with limited prior knowledge and unpaired omics data. Additionally, downstream biological analyses were conducted to highlight PRISM-GRN's real-world efficacy in improving the understanding of gene functions and finding GRNs.More specifically, for a given cell...
  8. ..., USA ↵10 Present address: Department of Biological Sciences and Ray and Stephanie Lane Department of Computational Biology, Carnegie Mellon University, Pittsburgh, PA 15213, USA Corresponding author: charles.gersbach@duke.eduAbstractA hallmark of heart disease is gene dysregulation and reactivation...
  9. .... Incorporation of this method of enhanced cavitation into FAIRE offers the potential for extending chromatin accessibility to clinical diagnosis and personalized medicine, while also enabling the exploration of gene regulatory mechanisms in archival samples.The dynamic regulation of chromatin architecture...
  10. ...genomics and community curation further improve gene annotations in the nematode Pristionchus pacificus. BMC Genomics 21: 708. doi:10.1186/s12864-020-07100-0 ↵Athanasouli M, Akduman N, Röseler W, Theam P, Rödelsperger C. 2023. Thousands of Pristionchus pacificus orphan genes were integrated...
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