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Wardhana, O.

Publications and source records attributed to Wardhana, O..

2 recordsLinked to original sources

Cell-type separability predicts annotation accuracy and outweighs algorithm choice: a factorial benchmark across seven scRNA paradigms

Automated cell-type annotation is a prerequisite for most single-cell RNA-sequencing (scRNA-seq) analyses, but the rapid proliferation of methods spanning marker-based, correlation-based, classical machine-learning, deep-learning, semi-supervised, large-language-model (LLM), and transformer foundation-model paradigms has outpaced head-to-head evaluation. Existing benchmarks rely on convenience samples of real datasets in which cell count, class imbalance, cell-type number, and differential-expression strength co-vary uncontrollably, precluding causal attribution of performance to any dataset property. To resolve this, we benchmarked 63 tools across seven paradigms using a Taguchi L9(34) orthogonal array that varies four dataset properties independently, progressively reconfiguring experimental control across five phases: fully controlled simulation, within-platform and cross-platform real-data validation, database-connected and LLM-based annotation under ontology-aware scoring, and fine-tuned foundation models. Using standardized oracle inputs and Cohen's {kappa}, we found that, within the ranges tested, the major paradigms achieved comparable accuracy. Accuracy was predicted near-linearly by the separability of cell types in a shared expression embedding, measured as k-nearest-neighbor (kNN) purity, a relationship that held across sequencing platforms and in fine-tuned foundation models. We attributed the vast majority of {kappa} variance to dataset structure and only a small share to tool identity. Computational cost traded against workflow accessibility rather than accuracy: accessible correlation-based and LLM-based approaches performed competitively, while foundation models matched them only after fine-tuning. Because our oracle design isolates algorithmic capability from upstream noise, these results reframe how methods should be selected: the field's near-term gains lie in strengthening infrastructure--prioritizing tool accessibility, standardized evaluation, and robustness to pipeline variation.

bioinformatics↗

Comparative Analysis of 3D Culture Methodologies in Prostate Cancer Cells

Three-dimensional (3D) cell culture models are increasingly utilized in cancer research to better replicate in vivo tumor microenvironments. This study examines the effects of different 3D scaffolding materials, including Matrigel, GelTrex, and the plant-based GrowDex, on prostate cancer cell lines, with a particular emphasis on neuroendocrine prostate cancer (NEPC). Four cell lines (LNCaP, LASCPC-01, PC-3, and KUCaP13) were cultured in these scaffolds to evaluate spheroid formation, cell viability, and gene expression. The results revealed that while all scaffolds supported cell viability, spheroid formation varied significantly: Matrigel promoted the most robust spheroids, especially for LASCPC-01, whereas GrowDex exhibited limitations for certain cell lines. Gene expression analysis indicated a consistent reduction in androgen receptor (AR) expression in LNCaP cells across all scaffolds, suggesting a potential shift towards a neuroendocrine phenotype. However, the expression of neuroendocrine markers varied depending on the scaffold and culture method, with the mini-domes method in Matrigel leading to decreased expression of both castration-resistant prostate cancer (CRPC) and NEPC markers. These findings highlight the scaffold-dependent variability in 3D culture outcomes and emphasize the need for standardized methodologies to ensure consistency and relevance in prostate cancer research. HighlightsO_LIComparing of Matrigel, GelTrex, and GrowDex in 3D prostate cancer culture C_LIO_LIIdentifying scaffold-dependent spheroid formation and gene expression shifts C_LIO_LIObserving consistent AR reduction and variable neuroendocrine marker changes C_LIO_LIHighlighting the need for standard 3D culture methods in cancer studies C_LI

cancer biology↗