Searching journal content for articles similar to Lawlor et al. 27 (2): 208.

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  1. ...Yang Zhou, Qiongyu Sheng, Jing Qi, Jiao Hua, Bo Yang, Lei Wan and Shuilin Jin School of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001 Corresponding author: jinsl@hit.edu.cnAbstractFor most biological and medical applications of single-cell transcriptomics...
  2. ...of bulk gene expression profiles is complicated by distinct cell type mixtures in each sample that obscure whether observed differences are actually caused by changes in the expression levels themselves or are simply a result of differing cell type compositions. Single-cell technology has made it possible...
  3. ...-wide transcriptomes of thousands of cells in a single scRNA-seq experiment (Aldridge and Teichmann 2020). Recent years have brought on continued development of single-cell technologies. The cost of single-cell experiments continues to cheapen. Technologies that enable the measurement of new information...
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  4. ...with each fit. The numbers of clusters selected were 5, 9, 11, 14, and 18, respectively. As shown in Supplemental Figure S24A, even when the number of clusters is increased from 5 to 18, the cells were still separated mainly by their gold standard cell type labels. Closer examination of the UMAPs revealed...
  5. ...over millions of cells that may vary widely, single-cell RNA-seq (scRNA-seq) can be used to investigate the subtle but crucial differences in transcriptomic landscape that differentiate cellular state. Populations of cells that possess very similar gross cellular phenotypes might have remarkably...
  6. ...(mBMDCs) stimulated with LPS, and compared these data to our previously generated full-length RNA-seq data (Garber et al. 2012). We also applied ESAT to single-cell RNA-seq from approximately 1000 rat pancreatic islet cells using a new droplet barcoding method for single-cell transcriptomics (Klein...
  7. ..., important biological insights into cell-type–specific expression signatures are revealed when comparing detailed RNA profiles of purified beta cells with those of whole islets or ‘‘nonbeta’’ cells. We find substantial evidence for differential expression between beta cells and islets, with more than 5000...
  8. ...transcriptome age index mirrors ontogenetic divergence patterns. Nature 468: 815–818. Ernst J, Kheradpour P,Mikkelsen TS, ShoreshN,Ward LD, EpsteinCB, Zhang X, Wang L, Issner R, Coyne M, et al. 2011. Mapping and analysis of chromatin state dynamics in nine human cell types. Nature 473: 43–49. Gaulton KJ, Nammo...
  9. ...clustering of samples by cell type, genotype, and age. A single linkage method was used for the hierarchical clustering of columns. (C) Principal component analysis (PCA) based on whole-transcriptome expression data highlights clear separation between different MN subtypes, with genotype and age also...
  10. ...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...
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