Searching journal content for articles similar to López-Cortegano et al. 35 (1): 43.

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  1. ...a systematic comparison between single-cell long-read and conventional short-read RNA sequencing techniques. The transcriptome of approximately 30,000 mouse retina cells was profiled using 1.54 billion Illumina short reads and 1.40 billion Oxford Nanopore Technologies long reads. Consequently, we identify 44...
  2. ....5%–56%) increase in the dnSNV rate with ART compared with naturally conceived mice (P = 0.017). Analysis of the dnSNV mutation spectrum identifies signatures attributable to germline DNA repair activity but reveals no differentially enriched signatures between cohorts. We observe no enrichment of dn...
  3. ...in the Twinkle subjects were more evenly distributed across the mitochondrial . The distribution of fusion event locations was distinct from the distribution of mtDNA deletion mutations breakpoints reported in long-read sequencing of normal aging muscle and in available online mtDNA mutation databases (Fig. 2C...
  4. ..., Spain; 10Gene Expression and mRNA Metabolism Laboratory, CIPF, 46012 Valencia, Spain ↵11 Joint first authorship. Corresponding author: aconesa@ufl.edu, aconesa@cipf.esAbstractHigh-throughput sequencing of full-length transcripts using long reads has paved the way for the discovery of thousands of novel...
  5. ...by nanopore sequencing of Cas9-targeted native DNA. DNA modifications trigger recognizable variation in the electrical current measured at the nanopore, enabling base-level modification analysis in long reads. Although this targeted test improves quantitation accuracy, it suffers from most of the same...
  6. ...on the same strand regardless of frame (Supplemental Table 19; Supplemental Fig. 31).Comparison with Pacific Biosciences (PacBio) long reads revealed that a substantial fraction of PRAM transcripts overlapped with these long reads and had matching splice junctions (Supplemental Fig. 32). Collectively...
  7. ...strains within a clade, then this would serve to homogenize the recombining sequences across strains, whereas nonrecombining regions would accumulate mutations independently in different strains (Fig. 4A, ‘‘Ongoing Recombination’’). Thus, the within-clade nucleotide divergence of recombined regions would...
  8. ...inactivation. Further analysis of the mutational landscape following APOBEC3A upregulation reveals a detailed spectrum of APOBEC3A-associated mutations, including indels, primarily 1 bp deletions, clustered mutations, and evidence of selective pressures acting on cells carrying the mutations. Our observations...
  9. ...to a mean coverage of 56-fold. This study identified a total of 1517 somatic mutations and validated 934 mutations by transcriptome sequencing. We detected recurrent mutations in 56 genes. Among them, 41 have not been described. The mutation rates varied widely among cell lines. The diversity...
  10. ...in length. However, little is known about the prevalence of recombination hotspots in insect s. Here we infer recombination rate and its fine-scale variation across the s of two social species from the insect order Blattodea: the termites Macrotermes bellicosus and Cryptotermes secundus. We used linkage...
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