Searching journal content for articles similar to Brown et al. 15 (5): 742.

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  1. .... Green arrowheads indicate predicted mRNA length of Ensembl v65 gene model. Red arrowheads indicate inferred mRNA lengths of novel 39 UTR extension isoforms. Asterisks denote background hybridization to ribosomal RNAs. 39 UTR lengthening in the mammalian brain Genome Research 815 www..org Several...
  2. ...assessments of protein-coding and transcriptome annotations separately. To add CDS annotations to StringTie and Scallop annotations, we used TransDecoder (https://github.com/TransDecoder/TransDecoder) to predict open reading frames (ORFs) and explicitly label features as CDS or UTR. Although there are other...
  3. ...challenging.We previously developed RiboPlotR to visualize Ribo-seq reads for all annotated isoforms of individual genes within their gene structures, including 5′ and 3′ untranslated regions (UTRs) and introns. It displays both RNA-seq coverage and Ribo-seq periodicity by color-coding reads from each reading...
  4. ...features that predict plant alternative translation initiation sites (TISs). (A) Illustration of the identified true-positive (TP; blue) and true-negative (TN; gray) TISs that were categorized based on the location of initiation codons (i.e., 5′ UTR, CDS, or 3′ UTR) and their sequences in a transcript...
  5. ...regions (UTRs) (Shabalina et al. 2010, 2014), prompt questions about the extent of AS contributions in diversifying the proteome.Existing approaches to analyze splicing and associated events have relied predominantly on pairwise comparisons of transcript architectures. For instance, the numeric symbolic...
  6. ...moment, resulting in k-mer-specific ion current shifts. RNA modifications can cause further shifts in the ion currents. Methods for detecting these alterations can be divided into two categories: de novo prediction, and comparative approaches. De novo prediction methods, including Tombo (Stoiber et al...
  7. ...for predicting essential genes. Methods Preparing fungal s for study We used the S. cerevisiae coding ORF list ( orf_coding.fasta.gz , revision 12/16/2004, available at ftp://-ftp.stanford.edu/pub/yeast/data_download/sequence/genomic_sequence/orf_dna/). This excludes 5′-UTR, 3′-UTR, intron sequences, and bases...
  8. ...). Transcripts are often specified for decay through the binding of RNA and protein factors to cis-regulatory elements within the 3′ untranslated region (UTR) (Ray et al. 2013; Vejnar et al. 2019). Cross talk between factors can lead to differential mRNA decay, such as RNA-binding proteins stabilizing...
  9. ...immunoprecipitation (ChIP) in 1984 followed by ChIP-qPCR and ChIP-seq, which allowed scientists to probe the full palette of DNA molecules bound by proteins of interest. A ChIP experiment begins by using formaldehyde to chemically cross-link DNA and protein molecules (Das et al. 2004). Nuclei are isolated...
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  10. ..., but there are multiple other reasons why clusters contain only moderately similar or unrelated protein sequences. These include cases in which one coding sequence has been predicted within introns, within UTRs, or on a different frame from another gene model. In a few cases, the differences could be the result of true...
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