Darya Orlova

ORCID: 0000-0003-1630-0828
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About
Contact & Profiles
Research Areas
  • Single-cell and spatial transcriptomics
  • Cell Image Analysis Techniques
  • T-cell and B-cell Immunology
  • Gene expression and cancer classification
  • Monoclonal and Polyclonal Antibodies Research
  • Immune Cell Function and Interaction
  • Genomics and Chromatin Dynamics
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • CAR-T cell therapy research
  • Respiratory Support and Mechanisms
  • vaccines and immunoinformatics approaches
  • Advanced Fluorescence Microscopy Techniques
  • Microfluidic and Bio-sensing Technologies
  • Bioinformatics and Genomic Networks
  • Advanced Biosensing Techniques and Applications
  • Cancer Genomics and Diagnostics
  • COVID-19 Clinical Research Studies
  • Nuclear Structure and Function
  • DNA Repair Mechanisms
  • Gene Regulatory Network Analysis
  • RNA Interference and Gene Delivery
  • Immune cells in cancer
  • Chemotherapy-induced cardiotoxicity and mitigation
  • Biomedical Text Mining and Ontologies

Cell Signaling Technology (United States)
2024-2025

National Research Mordovia State University
2023

Stanford University
2014-2019

Institute of Chemical Kinetics and Combustion
2007-2015

Czech Academy of Sciences
2009-2012

Czech Academy of Sciences, Institute of Biophysics
2009-2012

Masaryk University
2011

Siberian Branch of the Russian Academy of Sciences
2007

Novosibirsk State University
2007

Changes in the frequencies of cell subsets that (co)express characteristic biomarkers, or levels biomarkers on subsets, are widely used as indices drug response, disease prognosis, stem reconstitution, etc. However, although currently available computational “gating” tools accurately reveal subset and marker expression levels, they fail to enable statistically reliable judgements whether these differ significantly between/among subject groups. Here we introduce flow cytometry data analysis...

10.1371/journal.pone.0151859 article EN cc-by PLoS ONE 2016-03-23

Abstract Deciphering cell signaling pathways is essential for advancing our understanding of basic biology, disease mechanisms, and the development innovative therapeutic interventions. Recent advancements in multi-omics technologies enable us to capture information a more meaningful context. However, omics data inherently complex—high-dimensional, heterogeneous, extensive—making it challenging human interpretation. Currently, computational tools capable inferring from are very limited,...

10.1101/2025.02.06.636961 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2025-02-08

Abstract Troubling disparities in COVID-19–associated mortality emerged early, with nearly 70% of deaths confined to Black/African American (AA) patients some areas. However, targeted studies on this vulnerable population are scarce. Here, we applied multiomics single-cell analyses immune profiles from matching airways and blood samples Black/AA during acute SARS-CoV-2 infection. Transcriptional reprogramming infiltrating IFITM2+/S100A12+ mature neutrophils, likely recruited via the...

10.1182/bloodadvances.2022008834 article EN cc-by-nc-nd Blood Advances 2022-11-18

Polycomb group (PcG) proteins, organized into bodies, are important regulatory components of epigenetic processes involved in the heritable transcriptional repression target genes. Here, we asked whether acetylation can influence nuclear arrangement and function BMI1 protein, a core component complex, PRC1. We used time-lapse confocal microscopy, micro-irradiation by UV laser (355 nm) GFP technology to study dynamics protein. observed that was recruited UV-damaged chromatin simultaneously...

10.1002/jcp.22912 article EN Journal of Cellular Physiology 2011-07-05

Abstract Cancer immunotherapy has transformed the clinical approach to patients with malignancies, as profound benefits can be seen in a subset of patients. To identify this subset, biomarker analyses increasingly focus on phenotypic and functional evaluation tumor microenvironment determine if density, spatial distribution, cellular composition immune cell infiltrates provide prognostic and/or predictive information. Attempts have been made develop standardized methods evaluate routine...

10.1002/path.6274 article EN The Journal of Pathology 2024-03-25

Understanding the mechanism of T-cell activation and receptor (TCR) discrimination MHC-presented epitope peptides (pMHCs) remains an open problem. Machine learning (ML)-based prediction TCR specificity has gained considerable recent attention. However, capacity current models to generalize unseen during training is currently unknown. Here, we use a proprietary cancer-patient data set that profiles binding novel regions peptide space show generalization unsolved Specifically, while ML methods...

10.1101/2025.04.04.647165 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2025-04-07

We studied the elastic light-scattering properties of human blood neutrophils, both experimentally and theoretically. The experimental study was performed with a scanning flow cytometer measuring patterns (LSPs) individual cells over an angular range 5–60 deg. determined absolute differential cross sections neutrophils. also proposed optical model for neutrophil as sphere filled by small spheres prolate spheroids that correspond to granules segmented nucleus, respectively. This used in...

10.1117/1.2992140 article EN Journal of Biomedical Optics 2008-01-01

Part of the flow/mass cytometry data analysis process is aligning (matching) cell subsets between relevant samples. Current methods address this cluster-matching problem in ways that are either computationally expensive, affected by curse dimensionality, or fail when population patterns significantly vary Here, we introduce a quadratic form (QF)-based cluster matching algorithm (QFMatch) efficient and accommodates cases where locations differ (or even disappear appear) from sample to sample....

10.1038/s41598-018-21444-4 article EN cc-by Scientific Reports 2018-02-13

Abstract Unsupervised clustering is a powerful machine-learning technique widely used to analyze high-dimensional biological data. It plays crucial role in uncovering patterns, structure, and inherent relationships within complex datasets without relying on predefined labels. In the context of biology, data may include transcriptomics, proteomics, variety single-cell omics Most existing algorithms operate directly space, their performance be negatively affected by phenomenon known as curse...

10.1101/2024.04.18.589981 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2024-04-22

Abstract When examining datasets of any dimensionality, researchers frequently aim to identify individual subsets (clusters) objects within the dataset. The ubiquity multidimensional data has motivated replacement user-guided clustering with fully automated clustering. methods are designed make more accurate, standardized and faster. However, adoption these is still limited by lack intuitive visualization cluster matching that would allow users readily interpret automatically generated...

10.1038/s42003-019-0467-6 article EN cc-by Communications Biology 2019-06-20

ABSTRACT Recent advancements in transcriptomics and proteomics have opened the possibility for spatially resolved molecular characterization of tissue architecture with promise enabling a deeper understanding biology either homeostasis or disease. The wealth data generated by these technologies has recently driven development wide range computational methods. These methods requirement advanced coding fluency to be applied integrated across full spatial omics analysis process thus presenting...

10.1101/2022.08.22.504841 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-08-23

Although it is well known that chromosomes are non-randomly organized during interphase, not completely clear whether higher-order chromatin structure transmitted from mother to daughter cells. Therefore, we addressed the question of how rearranged interphase and heterochromatin pattern after mitosis. We additionally tested similarity arrangement in sister nuclei. noticed a very active cell rotation especially when histone hyperacetylation was induced or transcription inhibited. This natural...

10.1002/jcb.24208 article EN Journal of Cellular Biochemistry 2012-05-29

Abstract The ability to predict T-cell receptor (TCR) specificity computationally could revolutionize personalized immunotherapies, vaccine development, and the understanding of immunology autoimmune diseases. While progress depends on obtaining training data that represent vast range possible TCR-ligand pairs, systematic assessment modeling assumptions is equally important can begin with existing data. We illustrate this by evaluating two ideas currently present in field 1,2 : treating TCR...

10.1101/2024.10.23.619492 preprint EN cc-by 2024-10-28

<title>Abstract</title> The ability to predict T-cell receptor (TCR) specificity computationally could revolutionize personalized immunotherapies, vaccine development, and the understanding of immunology autoimmune diseases. While progress depends on obtaining training data that represent vast range possible TCR-ligand pairs, systematic assessment modeling assumptions is equally important can begin with existing data. We illustrate this by evaluating two ideas currently present in field:...

10.21203/rs.3.rs-5338858/v1 preprint EN cc-by Research Square (Research Square) 2024-10-29

2626 Background: Based on the clinical success of immuno-oncology therapeutics, tissue-based, biomarker analyses have shifted from a focus tumor cell phenotypes to spatial and functional immune environment. Distribution composition infiltrates shown prognostic or predictive value in various studies; however, standardized approaches categorize tumors into “Desert”, “Excluded” “Inflamed” immunophenotypes based density pattern are missing. This categorization is typically visual inspection...

10.1200/jco.2022.40.16_suppl.2626 article EN Journal of Clinical Oncology 2022-06-01

Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the ensuing COVID-19 pandemic have caused ∼40 million cases over 648,000 deaths in United States alone. Troubling disparities COVID-19-associated mortality emerged early, with nearly 70% of confined to Black/African-American (AA) patients some areas, yet targeted studies within this demographic are scant. Multi-omics single-cell analyses immune profiles from airways matching blood samples Black/AA revealed low viral...

10.1101/2021.06.02.446468 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-06-03

Summary The immune phenotype of a tumor is key predictor its response to immunotherapy 1–4 . Patients who respond checkpoint blockade generally present with tumors that are infiltrated by activated T cells, tumor-immune referred as ‘immune inflamed’ 5–7 However, not all inflamed therapy, and in addition the majority patients presents lack cells (‘immune desert’) or exclude periphery islet excluded’) 8 Despite importance these phenotypes patients, little known about their development,...

10.1101/2021.05.27.445482 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-05-28
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