Searching journal content for articles similar to Groet et al. 8 (4): 385.

Displaying results 1-10 of 5930
For checked items
  1. ...), NPC lines, and developmental timepoints, to generate a list of putative enhancer regions to investigate using the phNPC model. Whereas other enhancer mapping tools such as massively parallel reporter assays (MPRAs) have been used to identify putative enhancer regions in primary human cortical cells...
  2. ...High-resolution, genotype-free mapping of genetic 1 variation with CRI-SPA-Map 2 3 Sheila Lutz*, Megan Lawler†, Samuel Amidon†, Frank W. Albert* 4 Department of Genetics, Cell Biology, & Development, 5 University of Minnesota, 6 6-160 Jackson Hall, 321 Church St SE 7 Minneapolis, MN 55455, USA 8...
    OPEN ACCESS ARTICLEACCEPTED MANUSCRIPT
  3. ...coexpression modules with differential responses to environmental microbiota. Third, we link the microbial and host transcriptome data by predicting a global map of more than 2800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential...
  4. ...map of pseudobulk gene expression for each DEG group across ages. Right: Top significant GO and KEGG enrichments for genes in each DEG group in oligodendrocytes subclass. Early-up, early upregulated DEGs in aging; Late-up, late upregulated DEGs in aging; Early-down, early downregulated DEGs in aging...
  5. ...), making it difficult to map specific genes, like antimicrobial resistance (AMR) genes, to either the chromosome or mobile genetic elements. Additionally, short-read sequencing technologies like Illumina sequencing by synthesis remain relatively expensive, in terms of both price per and acquisition cost...
  6. ...mapping approaches were tested (Supplemental Figs. 7, 8). PlasFlow (v1.1.0) (Krawczyk et al. 2018) extracts chromosome contigs for downstream analysis without plasmid sequences. R was utilized to plot sequence motifs (Fig. 2B) with ggseqlogo (Wagih 2017) and a violin chart comparing base frequencies per...
  7. ...with the Connectivity Map (CMap) database and the drug–target interactome (Fig. 1C). This approach facilitated the identification of candidate repurposable drugs for each major brain cell type across AD progression.Overview of snRNA-seq and snATAC-seq data across ADNC progressionAD progression staging based on ADNC...
  8. ...insertion sequence. For deletions, we also observe higher counts for LR-GS up to 10 kb, after which we start to observe similar numbers from short reads (Fig. 2A). This is because such large deletions are readily detected by a lack of mapping reads (short or long), whereas detecting large insertions...
  9. .... Schematic overviews of key methodologies used for mapping R-loops. (A) In DRIP, fragmented genomic DNA is incubated with the S9.6 antibody to immunoprecipitate DNA–RNA hybrids for sequencing. (B) bisDRIP combines DRIP with nondenaturing bisulfite treatment to selectively deaminate ssDNA regions and convert...
  10. ...) Identification of error-prone sites in four bacteria defined by C2T or G2A substitution frequencies exceeding two. (D) Proportions and counts of accurately and inaccurately mapped bases at error-prone C and G sites in four bacterial s, respectively. Mapping reads were obtained from R9.4.1, R9.4.1 WGA, R10...
For checked items

Preprint Server