Searching journal content for articles similar to Blechschmidt et al. 9 (2): 158.

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  1. ...to ggRibo, GWIPS-viz plots Ribo-seq reads in a single color, which hinders the intuitive interpretation of reading frames (Supplemental Fig. S2B). Although RiboCrypt offers color-coded reading frames in the “gene” view, the reading frame is assigned based on the genomic sequence, and therefore...
  2. ...upstream sequence imparts a multifaceted role in regulation beyond the XCI.X-Chromosome inactivation (XCI) is a process by which female mammals compensate for the dosage of X-linked gene expression between sexes (Lyon 1961; Gayen et al. 2015, 2016). XCI is an excellent model system for understanding...
  3. ...NovaSeq 6000 instrument at the University of Chicago Genomics Core Facility (RRID:SCR_019196).Differential expression analysisTo identify genes differentially expressed between treatment conditions, we relied on well-established methods for analyzing bulk RNA sequencing data. Single-cell transcriptomes...
  4. ..., Florida 32611, USA; 4Department of Computer Science, University of Maryland, College Park, Maryland 20742, USA Corresponding author: nnoyes@umn.eduAbstractWe investigated the efficiency of target-enriched long-read sequencing (TELSeq) for detecting antimicrobial resistance genes (ARGs) and mobile genetic...
  5. ...embryo and A. thaliana cauline leaf samples, but only a single replicate was used for analyses.DNA-m6A loci genomic positionsA. thaliana gene and transposable element TSSs were identified using the “TAIR9_GFF3_genes_transposons.gff” annotation file downloaded from The Arabidopsis Information Resource...
  6. .... Associations between the recombination rate and base composition (A) and gene density (B) in 1-Mb genomic windows. (A) Association between the recombination rate and the nucleotide composition (GC content). (B) Association between the recombination rate and the density of coding sequences (CDS).Because we...
  7. ...sequence capture with or without the additional lysozyme step. (D) Violin plots of host gene UMI count, gene count, and mitochondria percentage (common measurements to QC single-cell and ST data) with or without lysozyme treatment, no significant difference could be observed. (E) Spatial dim plots showing...
  8. .... Nuclei were isolated by following the protocol provided by 10x Genomics (nuclei isolation for single-cell multiome ATAC + gene expression sequencing, CG00365, Rev A). The final nuclei concentration was adjusted to 3000 cell/µL in 1× nuclei buffer (10x Genomics). The sample was immediately submitted...
  9. ...RNAs in early pupae exert regulatory activities on their putative target genes during normal development, we analyzed our mRNA-seq data of WT across different stages. Enriched GO groups of genes with an increased mRNA level include “mitochondrion organization” (GO:0007005), “cuticle development” (GO:0042335...
  10. ...by different combinations of exons and introns, which cannot be accurately solved by Illumina reads. At the same time, the cost and scalability it offers is comparable to that of Illumina sequencing. We generated around 7 million dRNA reads in an organism with about 7000 genes. This high coverage and the lack...
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