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Autori principali: Cai, Xiao-Xuan, Liao, Jing-Shan, Ma, Jia-Jun, Pang, Yu-Xuan, Chen, Yi-Gang, Lin, Yang-Chi-Dung, Chen, Yi-Dan, Cao, Xin, Zhang, Yi-Cheng, Xu, Tao-Sheng, Lee, Tzong-Yi, Huang, Hsi-Yuan, Huang, Hsien-Da
Natura: Preprint
Pubblicazione: 2025
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Accesso online:https://arxiv.org/abs/2508.05692
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author Cai, Xiao-Xuan
Liao, Jing-Shan
Ma, Jia-Jun
Pang, Yu-Xuan
Chen, Yi-Gang
Lin, Yang-Chi-Dung
Chen, Yi-Dan
Cao, Xin
Zhang, Yi-Cheng
Xu, Tao-Sheng
Lee, Tzong-Yi
Huang, Hsi-Yuan
Huang, Hsien-Da
author_facet Cai, Xiao-Xuan
Liao, Jing-Shan
Ma, Jia-Jun
Pang, Yu-Xuan
Chen, Yi-Gang
Lin, Yang-Chi-Dung
Chen, Yi-Dan
Cao, Xin
Zhang, Yi-Cheng
Xu, Tao-Sheng
Lee, Tzong-Yi
Huang, Hsi-Yuan
Huang, Hsien-Da
contents microRNA are pivotal post-transcriptional regulators whose single-cell behavior has remained largely inaccessible owing to technical barriers in single-cell small-RNA profiling. We present SiCmiR, a two-layer neural network that predicts miRNA expression profile from only 977 LINCS L1000 landmark genes reducing sensitivity to dropout of single-cell RNA-seq data. Proof-of-concept analyses illustrate how SiCmiR can uncover candidate hub-miRNAs in bulk-seq cell lines and hepatocellular carcinoma, scRNA-seq pancreatic ductal carcinoma and ACTH-secreting pituitary adenoma and extracellular-vesicle-mediated crosstalk in glioblastoma. Trained on 6462 TCGA paired miRNA-mRNA samples, SiCmiR attains state-of-the-art accuracy on held-out cancers and generalizes to unseen cancer types, drug perturbations and scRNA-seq. We next constructed SiCmiR-Atlas, containing 632 public datasets, 9.36 million cells, 726 cell types, which is the first dedicated database of single-cell mature miRNA expression--providing interactive visualization, biomarker identification and cell-type-resolved miRNA-target networks. SiCmiR transforms bulk-derived statistical power into a single-cell view of miRNA biology and provides a community resource SiCmiR Atlas for biomarker discovery. SiCmiR Atlas is avilable at https://awi.cuhk.edu.cn/~SiCmiR/.
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institution arXiv
publishDate 2025
record_format arxiv
spellingShingle SiCmiR Atlas: Single-Cell miRNA Landscapes Reveals Hub-miRNA and Network Signatures in Human Cancers
Cai, Xiao-Xuan
Liao, Jing-Shan
Ma, Jia-Jun
Pang, Yu-Xuan
Chen, Yi-Gang
Lin, Yang-Chi-Dung
Chen, Yi-Dan
Cao, Xin
Zhang, Yi-Cheng
Xu, Tao-Sheng
Lee, Tzong-Yi
Huang, Hsi-Yuan
Huang, Hsien-Da
Genomics
microRNA are pivotal post-transcriptional regulators whose single-cell behavior has remained largely inaccessible owing to technical barriers in single-cell small-RNA profiling. We present SiCmiR, a two-layer neural network that predicts miRNA expression profile from only 977 LINCS L1000 landmark genes reducing sensitivity to dropout of single-cell RNA-seq data. Proof-of-concept analyses illustrate how SiCmiR can uncover candidate hub-miRNAs in bulk-seq cell lines and hepatocellular carcinoma, scRNA-seq pancreatic ductal carcinoma and ACTH-secreting pituitary adenoma and extracellular-vesicle-mediated crosstalk in glioblastoma. Trained on 6462 TCGA paired miRNA-mRNA samples, SiCmiR attains state-of-the-art accuracy on held-out cancers and generalizes to unseen cancer types, drug perturbations and scRNA-seq. We next constructed SiCmiR-Atlas, containing 632 public datasets, 9.36 million cells, 726 cell types, which is the first dedicated database of single-cell mature miRNA expression--providing interactive visualization, biomarker identification and cell-type-resolved miRNA-target networks. SiCmiR transforms bulk-derived statistical power into a single-cell view of miRNA biology and provides a community resource SiCmiR Atlas for biomarker discovery. SiCmiR Atlas is avilable at https://awi.cuhk.edu.cn/~SiCmiR/.
title SiCmiR Atlas: Single-Cell miRNA Landscapes Reveals Hub-miRNA and Network Signatures in Human Cancers
topic Genomics
url https://arxiv.org/abs/2508.05692