Searching journal content for articles similar to Gao et al. 32 (6): 1199.

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  1. ...). In particular, single-cell multi-omics technologies like SHARE-seq (Ma et al. 2020) can simultaneously profile transcriptomic and epigenomic data within individual cells, enabling the interrogation of cellular heterogeneity and molecular hierarchy (Cao et al. 2024). Consequently, numerous methods have emerged...
  2. ...demonstrates enhanced accuracy in detecting spatial domains, as evidenced across various benchmark data sets and technological platforms.Spatially resolved multi-omics technologies enable the profiling of multiple omic measurements, such as the transcriptome and proteome, in individual tissue sections, leading...
  3. ...) data set because it was primarily designed for short reads. (AUPR) Area under the precision-recall curve.To evaluate the feasibility of PanTax on real metagenomic data, we assessed its performance alongside several leading metagenomic profilers (according to BC distance in our simulated and mock...
  4. ...1 Title 1 Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals 2 conserved gene alterations linked to Parkinson’s disease 3 Running title: Substantia nigra aging linked to Parkinson 4 Kangli Wang1, Weikun Xia1, Yingli Gu1, Songpeng Zu1, Qian Yang2, Maria Luisa Amaral1...
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  5. ...imaging, multi-omics sequencing, and mass spectrometry (MS)–based proteome analyses in cKO oocytes. Although H3K9me1 was depleted only upon loss of EHMT1, H3K9me2 was decreased, and H3K9me2-enriched domains were eliminated equally upon loss of EHMT1 or EHMT2. Furthermore, there were more significant...
  6. ...fate toward specific lineages at a single-cell level. iTF-seq enables time course monitoring of transcriptome changes, and with biotinylated individual TFs, it provides a multi-omics approach to understanding the mechanisms behind TF-mediated cell fate changes. Our iTF-seq study in mouse embryonic stem...
  7. ..., such as those found in repeat expansion disorders, and for achieving precise haplotype phasing. Enhanced mappability improves variant detection and epigenetic profiling, facilitating a deeper understanding of genetic and epigenetic mechanisms underlying various diseases.Accurate haplotype assignment and phasing...
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  8. ...in dysregulation of metabolic pathways. We examined the direct effect of glucocorticoid exposure, low-dose dexamethasone (DEX), from embryonic day (E) 4 (before lineage specification) until E7 (blastocyst stage after mural–polar specification has initiated). On E7, we used a single-cell multi-omics approach...
  9. ...accessibility, and higher-order chromatin structure profiles for human and mouse early embryos. It incorporates customized analysis tools, such as “multi-omics visualization,” “Gene&Peak annotation,” “ZGA gene cluster,” “cis-regulation,” “synergistic regulation,” “promoter signal enrichment,” and “3D .” Users...
  10. ...and multi-omics algorithms, and an orthogonal in vitro screen (CRISPR-Cas9) targeting all ERGs revealed genes with driver roles within and across malignancies and shared driver mechanisms operating across multiple cancer types and hallmarks. This is the largest and most comprehensive analysis thus far...
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