Searching journal content for articles similar to Zhou et al. 33 (5): 750.

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  1. Method: A gene regulatory network–aware graph learning method for cell identity annotation in single-cell RNA-seq data
    • Mengyuan Zhao,
    • Jiawei Li,
    • Xiaoyi Liu,
    • Ke Ma,
    • Jijun Tang,
    • and Fei Guo
    Genome Res. July 2024 34: 1036-1051; Published in Advance August 12, 2024, doi:10.1101/gr.278439.123
    ....In single-cell transcriptome sequencing, high-resolution quantification of gene expression profiles provides insights into cellular heterogeneity and the molecular underpinnings of tissue phenotype variations (Kalucka et al. 2020; Argelaguet et al. 2021). Analyzing cell type composition using scRNA-seq...
  2. Method: Aggregation of recount3 RNA-seq data improves inference of consensus and tissue-specific gene coexpression networks
    • Prashanthi Ravichandran,
    • Princy Parsana,
    • Rebecca Keener,
    • Kasper D. Hansen,
    • and Alexis Battle
    Genome Res. September 2025 35: 2087-2103; Published in Advance July 17, 2025, doi:10.1101/gr.280808.125
    ...sizes for reliable GCN inference. recount3, a data set with 316,443 processed human RNA-seq samples, provides an opportunity to improve network reconstruction. However, GCN inference from public data is challenged by confounders and inconsistent labeling. To address this, we develop a pipeline...
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  3. Method: Recovering gene regulatory networks in single-cell multi-omics data with PRISM-GRN
    • Wenhao Zhang,
    • Lan Cao,
    • Xiaoxuan Gu,
    • Yongyu Long,
    • and Ying Wang
    Genome Res. January 2026 36: 142-158; Published in Advance October 9, 2025, doi:10.1101/gr.280757.125
    ...and target genes (Gao et al. 2023).Single-cell RNA sequencing (scRNA-seq) enables gene expression profiling at the individual cell level, revealing cellular heterogeneity with single-cell resolution and significantly enhancing the understanding of cell type–specific gene regulation (Chen and Liu 2022; Kartha...
  4. Method: Label-free selection of marker genes in single-cell and spatial transcriptomics with geneCover
    • An Wang,
    • Stephanie Hicks,
    • Donald Geman,
    • and Laurent Younes
    Genome Res. December 2025 35: 2744-2755; Published in Advance November 12, 2025, doi:10.1101/gr.280539.125
    ...for Imaging Science, Johns Hopkins University, Baltimore, Maryland 21218, USA Corresponding author: awang87@jhu.eduAbstractThe selection of marker gene panels is critical for capturing the cellular and spatial heterogeneity in the expanding atlases of single-cell RNA sequencing (scRNA-seq) and spatial...
  5. Method: Polyomino reconstructs spatial transcriptomic profiles with single-cell resolution via a region-allocation method
    • Quanyou Cai,
    • Lihui Lin,
    • Xin Liu,
    • and Jiekai Chen
    Genome Res. November 2025 35: 2513-2526; Published in Advance October 22, 2025, doi:10.1101/gr.280532.125
    ....Simulations of spatial detection noiseFor cell segmentation noise, we simulated ground-truth ST data with real single cells. Each spatial cell in the seqFISH+ data (Eng et al. 2019) was replaced by a single cell from the snRNA-seq data set (Tasic et al. 2018) derived from the same tissue. Let represent the overlapping...
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  6. Method: Deciphering context-specific gene programs from single-cell and spatial transcriptomics data with DeCEP
    • Lin Li,
    • Xianbin Su,
    • and Ze-Guang Han
    Genome Res. October 2025 35: 2300-2315; Published in Advance August 21, 2025, doi:10.1101/gr.279689.124
    .... Recent advancements in single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics (ST) technologies have empowered the comprehensive characterization of gene programs at both single-cell and spatial resolutions. Here, we present DeCEP, a computational framework designed to characterize context...
  7. Method: A unified analysis of atlas single-cell data
    • Hao Chen,
    • Nam D. Nguyen,
    • Matthew Ruffalo,
    • and Ziv Bar-Joseph
    Genome Res. May 2025 35: 1219-1233; Published in Advance February 18, 2025, doi:10.1101/gr.279631.124
    ...assumption of these technologies.The rapid expansion of single-cell technologies has introduced various sequencing platforms that produce data with different qualities. For example, in contrast to transcript end sequencing technologies, full-length scRNA-seq covers the entire sequence of RNA molecules...
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  8. Method: Accurate fusion transcript identification from long- and short-read isoform sequencing at bulk or single-cell resolution
    • Qian Qin,
    • Victoria Popic,
    • Kirsty Wienand,
    • Houlin Yu,
    • Emily White,
    • Akanksha Khorgade,
    • Asa Shin,
    • Christophe Georgescu,
    • Catarina D. Campbell,
    • Arthur Dondi,
    • Niko Beerenwinkel,
    • Francisca Vazquez,
    • Aziz M. Al'Khafaji,
    • and Brian J. Haas
    Genome Res. April 2025 35: 967-986; Published in Advance March 14, 2025, doi:10.1101/gr.279200.124
    ...short-read sequences. Recent advances in long-read isoform sequencing enable the detection of fusion transcripts at unprecedented resolution in bulk and single-cell samples. Here, we developed a new computational tool, CTAT-LR-Fusion, to detect fusion transcripts from long-read RNA-seq with or without...
    OPEN ACCESS ARTICLE
  9. Method: Cross-species cell-type assignment from single-cell RNA-seq data by a heterogeneous graph neural network
    • Xingyan Liu,
    • Qunlun Shen,
    • and Shihua Zhang
    Genome Res. January 2023 33: 96-111; Published in Advance December 16, 2022, doi:10.1101/gr.276868.122
    ...insights into evolutionary and developmental biology (Marioni and Arendt 2017). Cross-species integration and comparison of scRNA-seq data sets allow us to explore, at single-cell resolution, the origins of cellular diversity and evolutionary mechanisms that shape cellular form and function (Marioni...
  10. Method: Inferring disease progression stages in single-cell transcriptomics using a weakly supervised deep learning approach
    • Fabien Wehbe,
    • Levi Adams,
    • Jordan Babadoudou,
    • Samantha Yuen,
    • Yoon-Seong Kim,
    • and Yoshiaki Tanaka
    Genome Res. January 2025 35: 135-146; Published in Advance December 2, 2024, doi:10.1101/gr.278812.123
    ...is applicable across multiple independent single-cell RNA sequencing (scRNA-seq) data sets. Using the pretrained model of the PD scRNA-seq data set (midbrains of young and aged healthy donors and PD patients) (as used in Fig. 1; Adams et al. 2024), we inferred disease progression levels of individual cells...
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