Evidence map›Paper›PMID 40924538›Full record

ArticleBioinformatics (Oxford, England)2025

BISON: bi-clustering of spatial omics data with feature selection.

Bencong Zhu, Alberto Cassese, Marina Vannucci, Michele Guindani, Qiwei Li

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

5 authors.

Bencong ZhuDepartment of Statistics, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.ORCID 0009-0006-3661-1470
Alberto CasseseDepartment of Statistics, Computer Science, Applications "G. Parenti", University of Florence, Florence 50121, Italy.ORCID 0000-0001-5830-4136
Marina VannucciDepartment of Statistics, Rice University, Houston, TX 77005, United States.ORCID 0000-0002-7360-5321
Michele GuindaniDepartment of Biostatistics, University of California, Los Angeles, Los Angeles, CA 90024, United States.ORCID 0000-0002-6363-9907
Qiwei LiDepartment of Mathematical Sciences, The University of Texas at Dallas, Richardson, TX 75080, United States.ORCID 0000-0002-1020-3050

Funding

Developing novel algorithms for spatial molecular profiling technologiesR01GM141519 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI XIAO, GUANGHUA · 2021 to 2024
$1.4M
National Science Foundation # 1636933National Science Foundation # 1920920NIGMS NIH HHS R01 GM141519NIH HHS # 1R01GM141519
6 · The paper itself

Abstract

motivationThe advent of next-generation sequencing-based spatially resolved transcriptomics (SRT) techniques has reshaped genomic studies by enabling high-throughput gene expression profiling while preserving spatial and morphological context. Understanding gene functions and interactions in different spatial domains is crucial, as it can enhance our comprehension of biological mechanisms, such as cancer-immune interactions and cell differentiation in various regions. It is necessary to cluster tissue regions into distinct spatial domains and identify discriminating genes (DGs) that elucidate the clustering result, referred to as spatial domain-specific DGs. Existing methods for identifying these genes typically rely on a two-stage approach, which can lead to the phenomenon known as double-dipping.

resultsTo address the challenge, we propose a unified Bayesian latent block model that simultaneously detects a list of DGs contributing to spatial domain identification while clustering these DGs and spatial locations. The efficacy of our proposed method is validated through a series of simulation experiments, and its capability to identify DGs is demonstrated through applications to benchmark SRT datasets. AVAILABILITY AND IMPLEMENTATION: The R/C++ implementation of BISON is available at https://github.com/new-zbc/BISON.

Indexed as

Computational BiologyGene Expression ProfilingGenomicsSoftwareAlgorithmsAnimalsBayes TheoremCluster AnalysisHigh-Throughput Nucleotide SequencingHumansTranscriptome

Identifiers

PMID40924538
PMCPMC12463466

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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.