Searching journal content for articles similar to Havlak et al. 14 (4): 721.

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  1. ...Cell type–specific gene regulatory atlas prioritizes drug targets and repurposable medicines in Alzheimer's disease Yunxiao Ren1,2, Ming Hu3,4, Yang E. Li5, Andrew A. Pieper6,7,8,9,10,11, Jeffrey Cummings12 and Feixiong Cheng1,2,4,13 1Cleveland Clinic Genome Center, Cleveland Clinic Research...
  2. ...when corresponding single-cell data are not available. To verify the applicability of our devised signature in bulk tumors, we used RNA-seq from The Cancer Genome Atlas (TCGA) data sets and scored both our cancer-cell EMT and hallmark EMT signatures.Scores of the ANS-derived signature showed higher...
  3. .... More specialized tools for this approach include the Peak Browser at ChIP Atlas (Oki et al. 2018) or browsing ChIPBase (Huang et al. 2023), which is especially strong for ncRNAs but can also be used for mRNA genes. The Eukaryotic Promoter Database ExPASy has the useful Mass Genome Annotation Archive...
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  4. ...and mutations using data sets from tumor sequencing projects, such as The Cancer Genome Atlas (TCGA) (Hutter and Zenklusen 2018; The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020). These tools employ a variety of approaches, including analysis of mutations using gene sequences, protein...
  5. ....211733). These cell lines consist of healthy and cancer cells, thereby creating a diverse data set.To further diversify our validation data sets, we used ATAC-seq data of two COAD and two KIRP tumors from The Cancer Genome Atlas (TCGA) (Corces et al. 2018). These data sets have been made available...
  6. ...Ruhollah Shemirani1, Gillian M. Belbin1,9, Sinead Cullina1,2, Christa Caggiano1, Christopher R. Gignoux3,4, Noah Zaitlen5,6,7 and Eimear E. Kenny1,2,8 1Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA; 2Department of Genetics and Genomic Sciences...
  7. ....To further explore the different gene–gene relationships profiled in the HuBMAP (adult human) and human fetal atlases, for each tissue that is common between the two atlases, we identified unique gene modules in the gene-embedding components of each atlas (Supplemental Note 11). Notably, we observed...
  8. ...that the previously annotated “neural” cells were glia, in agreement with the authors of the Heart Cell Atlas (Kanemaru et al. 2023). Our analysis showed that male glia expressed XIST robustly (Fig. 1A–C). To study if this is specific to the heart, we then obtained human skeletal muscle scRNA-seq data for fibroblasts...
  9. ...and reference atlases has enabled the comparison of cell states across conditions, yet a gap persists in quantifying pathological shifts from healthy cell states. To address this gap, we introduce single-cell Pathological Shift Scoring (scPSS), which provides a statistical measure for how much a “query” cell...
  10. ...RNA-seq and scATAC-seq data and learning cross-modality relationship simultaneously. Genome Biol 23: 139. doi:10.1186/s13059-022-02706-x ↵Zhao J, Wang G, Ming J, Lin Z, Wang Y, Wu AR, Yang C. 2022. Adversarial domain translation networks for integrating large-scale atlas-level single-cell datasets. Nat Comput...
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