Searching journal content for articles similar to Valen et al. 19 (2): 255.

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  1. ..., and not independent promoters. Discussion Genome-wide analysis of core promoter architecture in D. melanogaster has been limited by the availability of TSS data. Previous studies have relied on 59 ESTs generated from large-insert cDNA libraries, including libraries constructed usingmethods that do not trap the 59 cap...
  2. ...in the discrimination of biological states, detection of differentially expressed genes, linearity of measurements, and quantification reproducibility. We found that the quantified levels of gene expression are largely comparable across platforms and conclude that CAGE and RNA-seq are complementary technologies...
  3. ....Visualization is emphasized in cell biology research to generate hypotheses and results. However, in omics studies, the visualization of sequencing data within genes of interest remains underutilized owing to a lack of appropriate tools. Recent advancements in plotting tools in the R programming language (R Core Team 2025...
  4. ...) Jitter plot of the number of genes with a promoter-proximal TSR in each sample. Error bars represent standard deviation.We next compared the dinucleotide frequencies of TSSs detected by STRIPE-seq, SLIC-CAGE, and nanoCAGE. STRIPE-seq and SLIC-CAGE both preferentially detected all four Y−1R+1 combinations...
  5. ...to the diversification of the transcriptome by generating a range of small RNAs and long coding and noncoding RNAs. Using genome-wide histone modification and RNA polymerase II occupancy data, we confirm that the vast majority of intraexonic CAGE tags are derived from post-transcriptional processing. By comparing exonic...
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