Searching journal content for articles similar to Liu et al. 26 (8): 1124.

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  1. ...development, including stem cell maintenance and cell differentiation. Recent advances in single-cell RNA-seq (scRNA-seq) revolutionized cell type–specific gene expression analysis. However, effective scRNA-seq quantification tools tailored for TEs are lacking, limiting our ability to dissect TE expression...
  2. ...that these results can be generalized for other types of functional sequencing assays, we calculated mapping error rates for the H3K4me3 histone modification ChIP-seq data set from the ENCODE consortium (Supplemental Fig. S37). Similar to the RNA-seq results, the error rate for reads overlapping homozygous variants...
  3. ...expression. However, these investigations have relied on cap analysis of gene expression (CAGE), which captures only the 5′ end of a transcript, or have used time series of limited duration and resolution.Here, we aim to use high temporal resolution rRNA-depleted total RNA-seq measurements to capture...
  4. ...of long 3′ UTR BDNF mRNA in spine morphology and synaptic plasticity in hippocampal neurons. Cell 134: 175–187. doi:10.1016/j.cell.2008.05.045 ↵Bailey TL. 2011. DREME: motif discovery in transcription factor ChIP-seq data. Bioinformatics 27: 1653–1659. doi:10.1093/bioinformatics/btr261 ↵Brennecke P...
  5. ...genomic data, including high-quality assembly and annotation for sika deer, remain lacking. This gap, combined with the challenges of determining regulatory relationships between regulatory elements (REs) and target genes (TGs) using standard ATAC-seq and histone ChIP-seq methods, have greatly hindered...
  6. ...of the cases. For example, transcriptional initiation of SNAPC4 is far (1k–2k bp) upstream of the RefSeq and GENCODE gene model 59 ends (Fig. 3B). CAGE finds a peak upstream, which is supported by ChIP-seq for H3K27 acetylation performed by the ENCODE Project (Ram et al. 2011). Such inaccuracies of gene models...
  7. ...a minor impact on TSS identification and quantification (r = 0.77) (Supplemental Fig. S5D,F).csRNA-seq identifies changes in activity at regulatory elements with higher dynamic range and better correlation with neighboring gene transcription changes than assays such as ATAC-seq or H3K27ac ChIP-seq...
  8. ...multi-omics profiling (gene expression and chromatin accessibility) on human and rat muscle samples. We capture type I and type II muscle fiber signatures, which are generally missed by existing single-cell RNA-seq methods. We perform cross-modality and cross-species integrative analyses on 33...
  9. ...of kilobases in length and low in abundance due to efficient processing by the endoribonuclease DROSHA, which initiates miRNA biogenesis. Accordingly, these transcripts are poorly represented in existing RNA-seq data sets and exhibit limited and inaccurate annotation in current transcriptome assemblies...
  10. ...(Creyghton et al. 2010). In ChIP-seq experiments performed on LCLs derived from five individuals heterozygous for rs73170828 (Kilpinen et al. 2013), there was substantially higher H3K27ac on the reference allele across the LCLs (P = 0.058, paired Wilcoxon test). Furthermore, there was an overall significant...
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