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  1. ...of how animals fight 32 infections. 33 Key words 34 Drosophila immunity/Immune-responsive enhancer/STARR-seq 35 36 Running Title 37 Genome-wide survey of fly immune enhancers 38 39 Introduction 40 When encountering pathogenic microbes, animals must regulate an effective immune response 41 to survive...
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  2. ..., 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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  3. ...-in orientations in vitro (Song et al. 2011, 2014). However, to what extent nucleosomes modulate CPD deamination in other sequence contexts and across the of intact cells remains unclear.Genome-wide sequencing methods have emerged as powerful tools to understand how different genomic and chromatin contexts impact...
  4. ...length as a function of the location of the midpoint of each fragment and colored the points based on their local density. The result is a near-nucleotide-resolution -wide view of chromatin occupancy for each deletion strain (Fig. 1D–F).View larger version: In this window In a new window Figure 1. Genome-wide...
  5. ...their genomic evolution is likely affected by adaptive processes.Genome-wide relaxation of purifying selectionThe overall increased dN/dS ratios in Orkney voles compared with continental voles suggest a lower effectiveness of selection in the population that experienced long-term isolation (Fig. 1...
  6. ..., Gronau I, Siepel A. 2014. Genome-wide inference of ancestral recombination graphs. PLoS Genet 10: e1004342. doi:10.1371/journal.pgen.1004342 ↵Schiffels S, Durbin R. 2014. Inferring human population size and separation history from multiple sequences. Nat Genet 46: 919–925. doi:10.1038/ng.3015 ↵Schiffels...
  7. ...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...
  8. ...abundances of accessible ssDNA and accessible DNA). (C) KAS-seq, ATAC-seq, and KAS-ATAC mitochondrial profiles in human GM12878 cells. (D) Fragment length distribution in biotin-ATAC-seq and KAS-ATAC libraries (GM12878 cells). (E) Genome-wide TSS metaprofiles for biotin-ATAC-seq and KAS-ATAC libraries (GM...
  9. ...haplotypes (Tibetan [n = 4] and Berkshire [n = 4]; measured by IDS) and among 82 diploid s in population-level analysis of purebred pigs (measured by pairwise IBS distances; see Supplemental Methods). Among the 82 diploids,12 from the six trios in this study (Berkshire, n = 6; Tibetan, n = 6) and 70...
  10. ...of H3K9me3 and H3K27me3 in the nondiapause (C), prediapause (D), and diapause (E) stages. (F–H) Venn diagram shows the number of genes with H3K9me3 peaks, H3K27me3 peaks, or both at the nondiapause (F), prediapause (G), and diapause (H) stages. (I–K) Genome-wide correlation plots showing correlation...
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