Searching journal content for articles similar to Groff et al. 29 (10): 1705.

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  1. ...Multitissue single-nucleus RNA-seq reveals cell type–specific regulatory patterns of alternative polyadenylation in pigs Qiuhan Wen1,2, Zhen Wang1, Qi Bao1, Tianli Ding1, Haihan Zhang3, Jianbo Li4, Zhuang Liu5, Jieping Huang2 and Guoqiang Yi1,6,7 1Shenzhen Branch, Guangdong Laboratory of Lingnan...
  2. ...evaluated using both simulated and real RNA-seq data sets from mouse (Mus musculus), chicken (Gallus gallus), zebrafish (Danio rerio), and roundworm (Caenorhabditis elegans) (Supplemental Table S3). For these benchmark tests, the Seq2Fun MEM mode aligns the translated reads to a database containing only...
  3. ...present an analytical framework tailored to TE expression quantification in scRNA-seq data sets. We systematically evaluated scRNA-seq reads that mapped to TEs and showed that quantifying TE expression in single cells using transcripts assembled from bulk RNA-seq effectively reduces noise. Applying our...
  4. ...-and-conquer, random projection (RP), weighted-based metaclustering, and similarity-based metaclustering. (B,C) Running time (B) and clustering performance (C) based on ARI (Hubert and Arabie 1985) of SHARP in 20 single-cell RNA-seq data sets with numbers of single cells ranging from 124 to 10 million (where data sets...
  5. ..., the stage of the embryo from which it came from was estimated by correlating its transcriptome with a whole-embryo bulk RNA seq time series (Hashimshony et al. 2015; Packer et al. 2019). The cells here cover a similar range of stages as those in the existing C. elegans embryo single-cell atlas (from...
  6. ...stages in different resolutions. When using these tools, alternatives are available for the species (human or mouse), signal type (“RNA-seq,” “ATAC-seq,” or “ChIP-seq”), or developmental stage (“oocyte,” “sperm,” “zygote,” “early two-cell,” “two-cell,” “late two-cell,” “four-cell,” “eight-cell,” “morula...
  7. ...–expression associations, neglect of biological relevance in evaluation, and poor performance in limited paired training data. To fill these gaps, we introduce scBOND, a bidirectional cross-modal translation framework tailored for scRNA-seq and scDNAm profiles. scBOND leverages a mixture-of-experts block to capture...
  8. ...obtained from the standard method.We also evaluated the robustness of the RNA-seq data generated in PARTAGE and found high reproducibility across replicates. Moreover, although PARTAGE RNA-seq was performed on low-input samples (20 K nuclei), it faithfully recapitulated the transcriptome obtained...
  9. ...information based on the RNA-seq data from The Cancer Genome Atlas (TCGA) (Weinstein et al. 2013). Here, we utilized the imputed profiles to select marker genes across the samples from the HEST-1k data set with different disease states and included the overlapped genes between the marker genes and genes from...
  10. ...as a promising resource for standardizing cell type annotations across studies. Although the current early-access release is limited to bulk RNA-seq data, the developers have announced that single-cell modalities are in active development. Once available, these synthetic single-cell data sets could provide...
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