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Sohn, K.-A.

Publications and source records attributed to Sohn, K.-A..

3 recordsLinked to original sources

CytoGate-Bench: an LLM benchmark for cross-panel cell gating in cytometry

In cytometry, the workhorse single-cell technology of clinical immunology, every study defines its own antibody panel and cell-type vocabulary, so a classifier trained on one cannot annotate the next. Immunologists instead annotate by manual gating, splitting one parent population at a time on a two-marker plot, down an expert-defined hierarchy. We introduce CytoGate-Bench, a benchmark that reformulates this per-step procedure as a zero-shot, panel-agnostic task for large language models. It comprises 23,646 expert-annotated instances re-curated from 11 public flow- and mass-cytometry cohorts spanning eight marker panels. Across six open- and closed-weight backbones, the strongest formulation draws one rectangular gate per candidate and falls within the range of trained, panel-specialized baselines. It degrades less under distribution shift. Walking the hierarchy stepwise outperforms predicting every cell type at once. Ablations trace the signal to the data distribution shape and curated marker priors. However, adding vision or a self-verification loop systematically tightens gates.

bioinformatics↗

Multi-layered network-based pathway activity inference using directed random walks: application to predicting clinical outcomes in urologic cancer

MotivationTo better understand the molecular features of cancers, a comprehensive analysis using multi-omics data has been conducted. Additionally, a pathway activity inference method has been developed to facilitate the integrative effects of multiple genes. In this respect, we have recently proposed a novel integrative pathway activity inference approach, iDRW, and demonstrated the effectiveness of the method with respect to dichotomizing two survival groups. However, there were several limitations, such as a lack of generality. In this study, we designed a directed gene-gene graph using pathway information by assigning interactions between genes in multiple layers of networks. ResultsAs a proof-of-concept study, it was evaluated using three genomic profiles of urologic cancer patients. The proposed integrative approach achieved improved outcome prediction performances compared with a single genomic profile alone and other existing pathway activity inference methods. The integrative approach also identified common/cancer-specific candidate driver pathways as predictive prognostic features in urologic cancers. Furthermore, it provides better biological insights into the prioritized pathways and genes in an integrated view using a multi-layered gene-gene network. Our framework is not specifically designed for urologic cancers and can be generally applicable for various datasets. AvailabilityiDRW is implemented as the R software package. The source codes are available at https://github.com/sykim122/iDRW.

bioinformatics↗

HiG2Vec: Hierarchical Representations of GeneOntology and Genes in the Poincare Ball

Knowledge manipulation of gene ontology (GO) and gene ontology annotation (GOA) can be done primarily by using vector representation of GO terms and genes for versatile applications such as deep learning. Previous studies have represented GO terms and genes or gene products to measure their semantic similarity using the Word2Vec-based method, which is an embedding method to represent entities as numeric vectors in Euclidean space. However, this method has the limitation that embedding large graph-structured data in the Euclidean space cannot prevent a loss of information of latent hierarchies, thus precluding the semantics of GO and GOA from being captured optimally. In this paper, we propose hierarchical representations of GO and genes (HiG2Vec) that apply Poincare embedding specialized in the representation of hierarchy through a two-step procedure: GO embedding and gene embedding. Through experiments, we show that our model represents the hierarchical structure better than other approaches and predicts the interaction of genes or gene products similar to or better than previous studies. The results indicate that HiG2Vec is superior to other methods in capturing the GO and gene semantics and in data utilization as well. It can be robustly applied to manipulate various biological knowledge. Availabilityhttps://github.com/JaesikKim/HiG2Vec Contactkasohn@ajou.ac.kr, Dokyoon.Kim@pennmedicine.upenn.edu

bioinformatics↗