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Kara, A.

Publications and source records attributed to Kara, A..

3 recordsLinked to original sources

Informing biologically relevant signal from spatial transcriptomic data

Visium is a spatial sequencing technology that utilizes messenger RNA (mRNA) to spatially map gene expression within tissues. Despite its potential, research utilizing deconvolution tools and exploring microenvironment dynamics remains challenging. We address this gap by benchmarking deconvolution tools across diverse biological contexts, identifying optimal methodologies. Subsequently, we introduce a novel pipeline integrating advanced deconvolution techniques and novel tools for reproducible tissue microenvironment analysis. Through this approach, we uncover intricate immune aggregate biology, highlighting the power of our methodology in unraveling complex biological phenomena.

bioinformatics↗

TarDis: Achieving Robust and Structured Disentanglement of Multiple Covariates

Addressing challenges in domain invariance within single-cell genomics necessitates innovative strategies to manage the heterogeneity of multi-source datasets while maintaining the integrity of biological signals. We introduce TarDis, a novel deep generative model designed to disentangle intricate covariate structures across diverse biological datasets, distinguishing technical artifacts from true biological variations. By employing tailored covariate-specific loss components and a self-supervised approach, TarDis effectively generates multiple latent space representations that capture each continuous and categorical target covariate separately, along with unexplained variation. Our extensive evaluations demonstrate that TarDis outperforms existing methods in data integration, covariate disentanglement, and robust out-of-distribution predictions. The models capacity to produce interpretable and structured latent spaces, including its pioneering work in ordered latent representations for continuous covariates, markedly enhances its utility in hypothesis-driven research. Consequently, TarDis offers a promising analytical platform for advancing scientific discovery, providing insights into cellular dynamics, and enabling targeted therapeutic interventions. Progress and potentialModern single-cell genomics provides an unprecedented view into cellular heterogeneity, yet the very richness that propels new discoveries also complicates downstream analysis. Gene-expression patterns emerge from overlapping biological processes (e.g., differentiation programs, disease progression) and extrinsic factors (e.g., laboratory protocols, technical artifacts). Disentanglement, in this context, aims to parse these intertwined influences into interpretable latent representations, a crucial step for elucidating how complex covariates shape cellular states. While methods that correct for batch effects have become standard, these strategies often fall short in achieving the deeper objective of capturing subtle, high-dimensional biological dynamics. In single-cell experiments, cells navigate intricate developmental trajectories, respond nonlinearly to environmental or pharmaceutical perturbations, and exhibit myriad context-specific behaviors. Without disentanglement, these diverse signals frequently remain intermingled, limiting biological interpretability and hindering hypothesis-driven research. Disentangling biological covariates is particularly vital for addressing nuanced questions in single-cell research. For example, in a disease model involving multiple genetic variants and variable drug dosing, researchers may wish to examine the effect of each variant independently or investigate how dosage influences a specific mutant background. Similarly, in developmental biology, uncovering how cells evolve across a continuum of pseudotime (e.g., from pluripotent to fully differentiated states) is critical for identifying the genes that orchestrate fate decisions while isolating the influence of developmental time from tissue-specific contexts, along with other confounding factors such as culture conditions, sample preparation, or donor genetic characteristics. Alternatively, disentangling lineage commitment signals from spatial patterning cues enables the identification of master regulators driving fate decisions. Moreover, by explicitly isolating and representing each covariate as an independent latent dimension, one can systematically navigate and interrogate a rich multidimensional covariate space. This approach extends beyond merely observing biological states, it enables exploration of novel or unmeasured cellular conditions through latent-space manipulations. For instance, disentangled latent spaces could allow researchers to computationally predict cellular responses at drug dosages or developmental stages that were never experimentally observed, significantly broadening the scope and predictive power of experimental datasets. Such analyses yield testable hypotheses for unexplored biological phenomena and enable informed planning of subsequent experimental validations. The challenge of covariate disentanglement stems fundamentally from the complexity of modeling joint distributions of gene expression conditioned simultaneously on multiple covariates, both categorical (e.g., tissue type, disease condition) and continuous (e.g., pseudotime, dosage). This is inherently an underdetermined problem because single-cell measurements represent only sparse snapshots within a vast combinatorial space of covariate conditions. Conventional modeling approaches often conflate correlated covariates, collapsing biological variability into ambiguous latent factors, and typically fail to explicitly create separate latent representations for disentangled covariates. Moreover, continuous covariates introduce an additional layer of complexity; yet discretizing them artificially imposes arbitrary boundaries, obscuring subtle transitions and hindering accurate capture of biological gradients. Therefore, preserving the continuous nature of such covariates in disentangled representations is critical, as it maintains their intrinsic ordering and enables researchers to discern nuanced biological shifts--such as identifying thresholds in dose-response relationships or characterizing gradual developmental transitions--in a naturally interpretable manner. The key idea in this paper is to devise a tailored deep generative model for systematically separating both categorical and continuous covariates into independent latent dimensions, while still ensuring coherent integration of the underlying gene-expression data. By explicitly targeting these covariates and preserving continuous variables as smooth, ordered latent axes, our approach clarifies complex interactions and uncovers nuanced patterns that remain concealed under standard analyses. The resulting disentangled representations can then support robust out-of-distribution generalizations, refined differential analyses, and more principled hypotheses about how diverse factors interact to drive cellular variation.

bioinformatics↗

Optimizing Niosome Formulations for Enhanced Cellular Applications: A Comparative Case Study with L-α-lecithin Liposomes

This study delves into the optimization of niosome production for biological applications, focusing on their emerging role as amphiphilic nanoparticles derived from nonionic surfactants, poised at the forefront of biomedical research. We aimed to formulate and characterize a diverse array of niosomal nanoparticles, with particular emphasis on process-related parameters and physicochemical characteristics. Critical thresholds for size, polydispersity, and zeta potential were established to identify parameters crucial for optimal niosomal formulations through a comprehensive investigation of concentrations, sonication times, ingredient ratios, and surfactant types. Leveraging MODDE(R) software, we generated ten optimized formulations from preliminary parameter screening. The proposed experimental model design by the software exhibited acceptable similarity to the obtained experimental results (F-score:0.83). The criteria for selection of the predicted experimental model formed based on targeted physicochemical considerations. To enhance half-life and penetration, especially in higher electrostatic regions like the Central Nervous System (CNS), we proposed a neutralized surface charge (-10 to 10 mV) while maintaining size within 100-200 nm and polydispersity below 0.5. Extended stability screening revealed periodic and extended Gaussian distributions for size and zeta potential to minimize flocculation and coagulation caused by neutralized surface charge. Notably, the cellular response performance of optimized niosomes was assessed via cellular binding, uptake, and viability in comparison to liposomes. Glioblastoma cell line (U-87) and granulocyte colony-stimulating factor (G-CSF) containing lymphoblastic leukemia cell line (NFS-60) were chosen to represent tumors developed in the CNS region and white blood cells, respectively, enabling a comprehensive comparative analysis with liposomes. The meticulous comparison between niosomes and liposomes revealed comparable cellular viability profiles on both U-87 and NFS-60 cell lines, highlighting their similarities in cellular interactions. Moreover, selected niosomal formulations demonstrated exceptional cellular uptake, either equaling or surpassing observed liposomal uptake. One of the most promising niosomes was selected and optimized to evaluate drug encapsulation performance of niosomes for further drug delivery adaptations by one of chemotherapy drugs, Paclitaxel (PTX). Cytotoxicity study was established with the most efficiently encapsulated niosome condition with human-derived fibroblasts (HDFs) and U-87 as the representation of healthy and cancerous cell lines. Results demonstrated 1:100 diluted PTX-loaded niosome in the certain concentration demonstrated favourable toxicity in U-87 than original PTX at the same concentration while not disturbing healthy HDFs. These findings underscore the potential of niosomes for reliable drug delivery, challenging the dominance of liposomal vehicles and presenting economically viable nanocarriers with significant implications for advancing biomedical research.

bioengineering↗