Searching journal content for articles similar to Foley et al. 29 (11): 1816.

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  1. ...Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson’s disease Kangli Wang,1 Weikun Xia,1 Yingli Gu,1 Songpeng Zu,1 Qian Yang,2 Maria Luisa Amaral,1 Yaozhi Wang,1 Allen Wang,2 Xiang-Dong Fu,3 William C. Mobley,4 and Bing Ren1...
  2. ...-specific networks. Central genes in consensus networks are enriched for evolutionarily constrained genes and ubiquitous biological pathways, whereas context-specific central nodes include tissue-specific transcription factors. The increased statistical power from data aggregation facilitates the derivation...
  3. ...of growth (P < 5 × 10−9, GO:BP, g:Profiler) (Supplemental Table 9).Postduplication FIEs are distributed in a wider variety of genes, with less than half occurring in known cancer genesFewer FIEs were identified postduplication compared with preduplication (LUAD, 18.5%; LUSC, 30.8% of total FIEs), and less...
  4. ...sample when performing sRNA-seq for dual profiling. In contrast, degradation bias (half-life analysis) and noise from housekeeping genes do not appear to have a significant effect upon or bias our approach. For the latter, Gene Ontology analysis identified tissue-specific pathways, reinforcing...
  5. ..., identify segmentally duplicated genes, and enable the phasing of reads (Logsdon et al. 2020). The phasing specifically allows for the assignment of haplotypes to pathogenic variants, enhancing diagnostic utility. LRS advancements enable the simultaneous measurement of DNAm profiles alongside genetic data...
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  6. ...in tissue sections. PCL-seq offers a more cost-effective and adaptable approach. We demonstrate its compatibility with both conventional fresh-frozen tissue sections and FFPE sections of mouse embryos. Moreover, PCL-seq achieves subcellular resolution, enabling the profiling of gene expression in distinct...
  7. ...in their gene expression levels (Fig. 1F; Supplemental Fig. S2). Overall, while PCS provided greater sequencing depth, our data demonstrated that both methods can capture a diverse range of transcripts from archival clinical samples, yielding highly concordant gene expression profiles.Differential gene...
  8. ..., preserving the spatial and morphological context of gene expression. Here, we describe expanding the chemistry for the Digital Spatial Profiling platform to quantify whole transcriptomes in human and mouse tissues using a wide range of spatial profiling strategies and sample types. We designed multiplexed...
  9. ...temporal patterns of TE expansion. Importantly, we uncover 50 robust coevolutionary signatures between 90 KZFPs and specific TE k-mer clusters, notably 51 involving 32 KZFPs that target Bovidae-specific LTR/ERVK clusters. Furthermore, 52 Bovinae-specific TEs impact gene structure by exonizing 14 genes...
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  10. ...and Koreski 2017) and are poorly captured by standard RNA-seq, making RNAPIIS5P profiling especially suitable for assessing their transcriptional regulation. Direct comparison of 40-day-old versus 15-day-old tissues shows widespread loss of RNAPIIS5P at most genes, accompanied by orders-of-magnitude higher...
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