Searching journal content for articles similar to Moles et al. 13 (11): 2467.

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  1. ...used for mitochondrial recovery and species identification. Long-read nanopore sequencers enable simultaneous reading of both DNA sequence and methylation and can multiplex samples for low-cost skimming. Here I present nanopore sequencing as a highly precise platform for global DNA methylation...
  2. ...fit the isoform model to data from the dividing MEFs. The parameters fit to these data revealed that global trends in isoform dynamics resembled those observed for contact-inhibited MEFs; in particular, conversion to the U-tailed isoform generally proceeded with the fastest rates, and these U...
  3. .... 2011). We used hypergeometric optimization of motif enrichment (HOMER) (Heinz et al. 2010), which can detect enriched motifs in a given list of sequences relative to a background list of sequences. We first compared sequences spanning alternative cassette exons and flanking introns to equivalent...
  4. ...replicates per time point (Fig. 1A). To ensure that we could normalize read counts even in the presence of global changes in transcription,we spiked the samenumber of permeable Drosophila cells into each sample prior to run-on (Booth et al. 2016). Samples were sequenced to a total combined depth of 334.3 M...
  5. ...set of A-to-I editing sites validated by the ICE method must be isolated for optimization of several ICE-seq parameters. As an extension of our previous analysis (Sakurai et al. 2010), we analyzed 1686 regions in human brain cDNA by the ICE method and identified 13,884 editing sites (Supplemental...
  6. ...by default based on our empirical observations on the MHC pan graph. But on other pan graphs, users may need to tune the parameter using the procedure described in the Results (see section “Effect of parameter c”).Further refinement of the proposed optimization framework is necessary to align...
  7. ...optimize the TSS-seq protocol to enhance sensitivity and accuracy. Specifically, we refine enzymatic reactions for decapping and RNA ligation and incorporate 5′ oligonucleotides containing unique molecular identifiers (UMIs) and barcodes to enable accurate quantification and sample multiplexing. The TT...
  8. ...distribution to derive mean and standard deviation parameters (Fig. 3A, left). We then applied this parameterized model to the aggregated sequencing counts (Supplemental Fig. S6); discrepancies between the predicted and observed data revealed GC-content-related biases (Fig. 3A, right). We repeated this process...
  9. ...Design optimization methods for genomic DNA tiling arrays Paul Bertone 1 , 3 , Valery Trifonov 2 , Joel S. Rozowsky 3 , Falk Schubert 2 , Olof Emanuelsson 3 , John Karro 3 , Ming-Yang Kao 4 , Michael Snyder 1 , 3...
  10. ...of constructing a valid control gene set. Overall, ANS induced the smallest bias, confirming the proposed strategy for control gene selection as the optimal one.The influence of cell-type proportions, batch effects, signature length, and inclusion of irrelevant genes on gene signature scoringThe mean control...
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