Evidence map›Paper›PMID 42418828›Full record

ArticleBriefings in bioinformatics2026

STGBench: sequencing-level spatial DNA-RNA simulation for multimodal and virtual cell-oriented benchmarking of genomic alterations.

Shenjie Wang, Yuhang Li, Xiaonan Wang, Xuwen Wang, Tianci Wang, Shuanying Yang, Jiayin Wang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shenjie WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710049, China.
Yuhang LiSchool of Computer Science and Technology, Xi'an Jiaotong University, 28 Xianning West Road, Beilin, Xi'an 710049, China.
Xiaonan WangNanjing Geneseeq Technology Inc., 128 Huakang Road, Pukou, Nanjing 211800, China.
Xuwen WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710049, China.
Tianci WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710049, China.
Shuanying YangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710049, China.
Jiayin WangDepartment of Respiratory Medicine, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, Xiwu Road, Xincheng District, Xi'an 710049, China.ORCID 0000-0002-3862-6557

Funding

China Postdoctoral Science Foundation 2025M771554National Natural Science Foundation of China 62402376National Natural Science Foundation of China 62572389National Natural Science Foundation of China T2541083
6 · The paper itself

Abstract

Spatially resolved genomics and transcriptomics are reshaping our understanding of tumor evolution and therapeutic resistance, yet benchmarking spatial copy number variation (CNV), single-nucleotide variant (SNV), and spatial mutation-burden proxy analyses is constrained by the scarcity of datasets with known ground truth. Existing simulators often produce only count matrices, lack matched DNA-RNA outputs, or do not propagate genomic variation to sequencing-level signals, limiting end-to-end benchmarking of multi-omics pipelines, including virtual cell-oriented multimodal benchmarks. Here, we present STGBench, a sequencing-level spatial DNA-RNA simulator that generates paired DNA-seq alignments (BAM files) and matched gene expression matrices on a user-defined 2D tissue grid. STGBench builds tissue masks from geometric templates or image-derived masks, overlays spatial CNV landscapes and SNV/VAF fields in boundary, gradient, and nested modes, and synthesizes DNA and RNA readouts by coupling copy number states to expression under a negative binomial model with spatially correlated technical effects; outputs are directly consumable by downstream tools. Using AneuFinder on simulated DNA data, spatial CNV profiles are recovered with Pearson r up to 0.855. Applying InferCNV to simulated transcriptomes, CNV-driven expression signatures are reproduced (r up to 0.996) and support unsupervised structure consistent with clonal organization; DNA-derived and RNA-inferred CNVs show concordance (r ≈ 0.77). CellSNP recovers diverse spatial SNV patterns from simulated reads, and IGV inspection confirms realistic allelic balance and CNV-associated coverage shifts at nucleotide resolution. Collectively, STGBench provides a controllable benchmark generator for spatial CNV/SNV and mutation-burden analyses with explicit ground truth across paired DNA-RNA modalities. STGBench is open source at https://github.com/Icarus200110/STGBench.

Indexed as

GenomicsRNASequence Analysis, DNASequence Analysis, RNASoftwareBenchmarkingComputer SimulationDNA Copy Number VariationsHumansMutationPolymorphism, Single NucleotideRNAmultimodal benchmarkingprobabilistic generative modelsequencing-level simulationspatial clonal heterogeneitytumor mutation burden

Identifiers

PMID42418828
PMCPMC13345378

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.