Searching journal content for articles similar to Son et al. 15 (3): 443.

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  1. ...coding gene expression with qPCR-validated targets. Our findings demonstrate that quantifying mRNA fragments from sRNA-seq experiments provides a reliable approach to investigate microRNA–mRNA interactions when total RNA-seq is unavailable.The analysis of gene expression is a cornerstone of functional...
  2. ..., and libraries were prepared for stranded mRNA sequencing. These standard analyses confirmed the close alignment of RT programs with compartmentalization as measured by Hi-C, as well as enrichment of active gene expression in active-early replicating genomic compartments (Fig. 3A). However, these data sets were...
  3. ...with their corresponding mRNA source and property used for method evaluationThe mRFP expression data set (Nieuwkoop et al. 2023) profiles protein production levels for several gene variants in E. coli. The fungal expression data set (Grigoriev et al. 2014; Wint et al. 2022) includes CDSs >150 bp from a wide range...
  4. .... Epigenetic treatment induces expression of the LTR12 families CAGE-seq (Cap Analysis of Gene Expression sequencing) is a highthroughput sequencing-based technique that quantitatively analyzes the 5' end of mRNA molecules, which addresses technical limitations encountered in conventional RNA-seq methodologies...
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  5. ...for further regulatory analysis (Supplemental File S9; modERNresource GitHub, https://github.com/modERNresource).Distribution of peaks and metapeaks relative to protein-coding genesTo evaluate the correlation between TF binding sites and mRNA abundance as measured in other experiments, we assigned the binding...
  6. .... 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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  7. ...are largely unknown. Here, we profile -wide changes to gene expression and chromatin structure in cardiomyocytes derived from human pluripotent stem cells. We identify and characterize a gene regulatory element essential for regulating MYH6 expression, which encodes human fetal myosin. Using chromatin...
  8. ...(PeqLab) and a Qubit 2.0 Fluorometer. The samples were shipped to Novogene for library preparation and messenger RNA (mRNA) sequencing. Libraries were sequenced as 150-bp paired-end reads on an Illumina NovoSeq 6000 platform.RNA-seq and coexpression network analysisFor the coexpression analysis, we...
  9. ..., as recently exemplified by the gene encoding the transcription factor SOX9 (Naqvi et al. 2023), these regulatory changes are associated with differences in phenotype and disease risk (Albert and Kruglyak 2015). To our knowledge, there exist currently no assays that measure the viable dosage range of mRNA...
  10. ...with sheep (Ovis aries) and Tasmanian devil (S. harrisii) tissue atlases, including reliably profiled protein-coding mRNA genes (breadth of coverage >10%), and with shared homologous loci among sheep, Tasmanian devil, and the thylacine (N = 261) (Supplemental Table 27). In this case, both thylacine skeletal...
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