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  1. ..., Bruhm DC, Jensen SØ, Medina JE, Hruban C, White JR, et al. 2019. Genome-wide cell-free DNA fragmentation in patients with cancer. Nature 570: 385–389. doi:10.1038/s41586-019-1272-6 ↵De Coster W, Weissensteiner MH, Sedlazeck FJ. 2021. Towards population-scale long-read sequencing. Nat Rev Genet 22: 572...
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  2. ...of nascent RNA identifies a unified architecture of initiation regions at mammalian promoters and enhancers. Nat Genet 46: 1311–1320. doi:10.1038/ng.3142 ↵Crawford GE, Holt IE, Whittle J, Webb BD, Tai D, Davis S, Margulies EH, Chen Y, Bernat JA, Ginsburg D, et al. 2006. Genome-wide mapping of DNase...
  3. ...Genome-wide patterns of selection–drift variation strongly associate with organismal traits across the green plant lineage Kavitha Uthanumallian1, Andrea Del Cortona2, Susana M. Coelho3, Olivier De Clerck2, Sebastian Duchene4,5 and Heroen Verbruggen1,6 1Melbourne Integrative Genomics, School of Bio...
  4. ..., Isogai T, Suzuki Y, Akimitsu N. 2012. Genome-wide determination of RNA stability reveals hundreds of short-lived noncoding transcripts in mammals. Genome Res 22: 947–956. doi:10.1101/gr.130559.111 ↵Thomson DW, Bracken CP, Goodall GJ. 2011. Experimental strategies for microRNA target identification...
  5. ...regions and the stability of the Z-RNA sequences identified in this study will provide better understanding of Z-RNA formation in the noncoding transcriptome.In summary, we provide a comprehensive data set of predicted noncanonical secondary structures throughout the long noncoding transcriptome...
  6. ..., and long noncoding RNA (lncRNA) transcripts (P<0.01). To experimentally validate the computationally identified isoform switches, we used RT-qPCR to measure the relative abundance of specific transcript variants for three representative genes (ATP2A2, TPM2, and GCNT2) at D4 and D30. For ATP2A2 and TPM2...
  7. ..., revolutionizing the field of human genetics (Tam et al. 2019). Despite these successes, the interpretation of GWAS signals represents a challenging task as they are often located within noncoding regions of the and manifest as complex linkage disequilibrium (LD) blocks where identification of the causal variant...
  8. .... 97 2020). 98 A recent study using the same Bru-seq and BruChase-seq datasets analyzed 99 here reported that allele-specific genetic variants can affect RNA stability by altering 100 conserved binding sequences of miRNAs and RNA-binding proteins (Huang et al. 101 2025). Many of the genes that have...
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  9. .... Misregulation of transposable elements, coding genes, and small regulatory RNAs was more widespread in the bB2 compared with the nB2 hybrids, which is a plausible explanation for the differential phenotypes between the two hybrids. Our results show that regulation of the C. briggsae is strongly affected...
  10. ...are enriched with YR nucleotides (IUPAC nomenclature), this determination was based on only 88 promoters (Hawley and McClure 1983). Genome-wide studies based on mapping RNA 5′ ends have found the YR motif to be enriched, with 79% of the +1 nucleotide being an R (Kim et al. 2012), whereas another study had R...
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