전체 논문 (18편 · 1/1)
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Co-mapping clonal and transcriptional heterogeneity in somatic evolution via GoT-Multi.
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Charting clonal evolution and behavior with GoT-Multi.
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Analysis of error profiles of indels and structural variants in deep-sequencing data.
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Hi-C for genome-wide detection of enhancer-hijacking rearrangements in routine lymphoid cancer biopsies.
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Predictive prioritization of enhancers associated with pancreatic disease risk.
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Predominant mutated non-canonical tumor-specific antigens identified by proteogenomics demonstrate immunogenicity and tumor suppression in CRC.
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Holistic determination of ends of cfDNA molecules.
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Cellular senescence in human liver under normal aging and cancer.
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Microbial single-cell omics in situ.
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Single-cell eQTL mapping reveals cell-type-specific genetic regulation in lung cancer.
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Hist2Cell: Deciphering fine-grained cellular architectures from histology images.
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Phenotypic pleiotropy of missense variants in human B cell confinement receptor P2RY8.
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Decoding missense variants pleiotropy in the immune GPCR P2RY8.
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CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST.
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Single-cell eQTL mapping reveals cell-type-specific genes associated with the risk of gastric cancer.
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Deciphering genetic regulation at single-cell resolution in gastric cancer.
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Identification of biomarkers and potential therapeutic targets for pancreatic cancer by proteomic analysis in two prospective cohorts.
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Molecular signature incorporating the immune microenvironment enhances thyroid cancer outcome prediction.