Alexandr A. Kalinin

Kirill Prokhorov, Alexandr A. Kalinin

Acne, a prevalent skin condition, necessitates precise severity assessment for effective treatment. Acne severity grading typically involves lesion counting and global assessment. However, manual grading suffers from variability and inefficiency, highlighting the need for automated tools. Recently, label distribution learning (LDL) was proposed as an effective framework for acne image grading, but its effectiveness is hindered by severity scales that assign varying numbers of lesions to different severity grades. Addressing these limitations, we proposed to incorporate severity scale information into lesion counting by combining LDL with label smoothing, and to decouple if from global assessment. A novel weighting scheme in our approach adjusts the degree of label smoothing based on the severity grading scale. This method helped to effectively manage label uncertainty without compromising class distinctiveness. Applied to the benchmark ACNE04 dataset, our model demonstrated improved performance in automated acne grading, showcasing its potential in enhancing acne diagnostics. The source code is publicly available at http://github.com/openface-io/acne-lds.

Alexandr A. Kalinin, Anne E. Carpenter, Shantanu Singh et al.

Quantitative analysis of multidimensional biological images is useful for understanding complex cellular phenotypes and accelerating advances in biomedical research. As modern microscopy generates ever-larger 2D and 3D datasets, existing computational approaches are increasingly limited by their scalability, efficiency, and integration with modern scientific computing workflows. Existing bioimage analysis tools often lack application programmable interfaces (APIs), do not support graphics processing unit (GPU) acceleration, lack broad 3D image processing capabilities, and/or have poor interoperability for compute-heavy workflows. Here, we introduce cubic, an open-source Python library that addresses these challenges by augmenting widely used SciPy and scikit-image APIs with GPU-accelerated alternatives from CuPy and RAPIDS cuCIM. cubic's API is device-agnostic and dispatches operations to GPU when data reside on the device and otherwise executes on CPU, seamlessly accelerating a broad range of image processing routines. This approach enables GPU acceleration of existing bioimage analysis workflows, from preprocessing to segmentation and feature extraction for 2D and 3D data. We evaluate cubic both by benchmarking individual operations and by reproducing existing deconvolution and segmentation pipelines, achieving substantial speedups while maintaining algorithmic fidelity. These advances establish a robust foundation for scalable, reproducible bioimage analysis that integrates with the broader Python scientific computing ecosystem, including other GPU-accelerated methods, enabling both interactive exploration and automated high-throughput analysis workflows. cubic is openly available at https://github$.$com/alxndrkalinin/cubic

Alexander Buslaev, Alex Parinov, Eugene Khvedchenya et al.

Data augmentation is a commonly used technique for increasing both the size and the diversity of labeled training sets by leveraging input transformations that preserve output labels. In computer vision domain, image augmentations have become a common implicit regularization technique to combat overfitting in deep convolutional neural networks and are ubiquitously used to improve performance. While most deep learning frameworks implement basic image transformations, the list is typically limited to some variations and combinations of flipping, rotating, scaling, and cropping. Moreover, the image processing speed varies in existing tools for image augmentation. We present Albumentations, a fast and flexible library for image augmentations with many various image transform operations available, that is also an easy-to-use wrapper around other augmentation libraries. We provide examples of image augmentations for different computer vision tasks and show that Albumentations is faster than other commonly used image augmentation tools on the most of commonly used image transformations. The source code for Albumentations is made publicly available online at https://github.com/albu/albumentations

Alexey Shvets, Vladimir Iglovikov, Alexander Rakhlin et al.

Accurate detection and localization for angiodysplasia lesions is an important problem in early stage diagnostics of gastrointestinal bleeding and anemia. Gold-standard for angiodysplasia detection and localization is performed using wireless capsule endoscopy. This pill-like device is able to produce thousand of high enough resolution images during one passage through gastrointestinal tract. In this paper we present our winning solution for MICCAI 2017 Endoscopic Vision SubChallenge: Angiodysplasia Detection and Localization its further improvements over the state-of-the-art results using several novel deep neural network architectures. It address the binary segmentation problem, where every pixel in an image is labeled as an angiodysplasia lesions or background. Then, we analyze connected component of each predicted mask. Based on the analysis we developed a classifier that predict angiodysplasia lesions (binary variable) and a detector for their localization (center of a component). In this setting, our approach outperforms other methods in every task subcategory for angiodysplasia detection and localization thereby providing state-of-the-art results for these problems. The source code for our solution is made publicly available at https://github.com/ternaus/angiodysplasia-segmentatio

Alexey Shvets, Alexander Rakhlin, Alexandr A. Kalinin et al.

Semantic segmentation of robotic instruments is an important problem for the robot-assisted surgery. One of the main challenges is to correctly detect an instrument's position for the tracking and pose estimation in the vicinity of surgical scenes. Accurate pixel-wise instrument segmentation is needed to address this challenge. In this paper we describe our winning solution for MICCAI 2017 Endoscopic Vision SubChallenge: Robotic Instrument Segmentation. Our approach demonstrates an improvement over the state-of-the-art results using several novel deep neural network architectures. It addressed the binary segmentation problem, where every pixel in an image is labeled as an instrument or background from the surgery video feed. In addition, we solve a multi-class segmentation problem, where we distinguish different instruments or different parts of an instrument from the background. In this setting, our approach outperforms other methods in every task subcategory for automatic instrument segmentation thereby providing state-of-the-art solution for this problem. The source code for our solution is made publicly available at https://github.com/ternaus/robot-surgery-segmentation

Alexander Rakhlin, Alexey Shvets, Vladimir Iglovikov et al.

Breast cancer is one of the main causes of cancer death worldwide. Early diagnostics significantly increases the chances of correct treatment and survival, but this process is tedious and often leads to a disagreement between pathologists. Computer-aided diagnosis systems showed potential for improving the diagnostic accuracy. In this work, we develop the computational approach based on deep convolution neural networks for breast cancer histology image classification. Hematoxylin and eosin stained breast histology microscopy image dataset is provided as a part of the ICIAR 2018 Grand Challenge on Breast Cancer Histology Images. Our approach utilizes several deep neural network architectures and gradient boosted trees classifier. For 4-class classification task, we report 87.2% accuracy. For 2-class classification task to detect carcinomas we report 93.8% accuracy, AUC 97.3%, and sensitivity/specificity 96.5/88.0% at the high-sensitivity operating point. To our knowledge, this approach outperforms other common methods in automated histopathological image classification. The source code for our approach is made publicly available at https://github.com/alexander-rakhlin/ICIAR2018

Alán F. Muñoz, Tim Treis, Alexandr A. Kalinin et al.

Biological image analysis has traditionally focused on measuring specific visual properties of interest for cells or other entities. A complementary paradigm gaining increasing traction is image-based profiling - quantifying many distinct visual features to form comprehensive profiles which may reveal hidden patterns in cellular states, drug responses, and disease mechanisms. While current tools like CellProfiler can generate these feature sets, they pose significant barriers to automated and reproducible analyses, hindering machine learning workflows. Here we introduce cp_measure, a Python library that extracts CellProfiler's core measurement capabilities into a modular, API-first tool designed for programmatic feature extraction. We demonstrate that cp_measure features retain high fidelity with CellProfiler features while enabling seamless integration with the scientific Python ecosystem. Through applications to 3D astrocyte imaging and spatial transcriptomics, we showcase how cp_measure enables reproducible, automated image-based profiling pipelines that scale effectively for machine learning applications in computational biology.

Alexandr A. Kalinin, Paula Llanos, Theresa Maria Sommer et al.

Microscopy enables direct observation of cellular morphology in 3D, with transmitted-light methods offering low-cost, minimally invasive imaging and fluorescence microscopy providing specificity and contrast. Virtual staining combines these strengths by using machine learning to predict fluorescence images from label-free inputs. However, training of existing methods typically relies on loss functions that treat all pixels equally, thus reproducing background noise and artifacts instead of focusing on biologically meaningful signals. We introduce Spotlight, a simple yet powerful virtual staining approach that guides the model to focus on relevant cellular structures. Spotlight uses histogram-based foreground estimation to mask pixel-wise loss and to calculate a Dice loss on soft-thresholded predictions for shape-aware learning. Applied to a 3D benchmark dataset, Spotlight improves morphological representation while preserving pixel-level accuracy, resulting in virtual stains better suited for downstream tasks such as segmentation and profiling.

Benjamin D. Lee, Anthony Gitter, Casey S. Greene et al.

Machine learning is a modern approach to problem-solving and task automation. In particular, machine learning is concerned with the development and applications of algorithms that can recognize patterns in data and use them for predictive modeling. Artificial neural networks are a particular class of machine learning algorithms and models that evolved into what is now described as deep learning. Given the computational advances made in the last decade, deep learning can now be applied to massive data sets and in innumerable contexts. Therefore, deep learning has become its own subfield of machine learning. In the context of biological research, it has been increasingly used to derive novel insights from high-dimensional biological data. To make the biological applications of deep learning more accessible to scientists who have some experience with machine learning, we solicited input from a community of researchers with varied biological and deep learning interests. These individuals collaboratively contributed to this manuscript's writing using the GitHub version control platform and the Manubot manuscript generation toolset. The goal was to articulate a practical, accessible, and concise set of guidelines and suggestions to follow when using deep learning. In the course of our discussions, several themes became clear: the importance of understanding and applying machine learning fundamentals as a baseline for utilizing deep learning, the necessity for extensive model comparisons with careful evaluation, and the need for critical thought in interpreting results generated by deep learning, among others.

Roman Solovyev, Alexandr A. Kalinin, Tatiana Gabruseva

Adequate blood supply is critical for normal brain function. Brain vasculature dysfunctions such as stalled blood flow in cerebral capillaries are associated with cognitive decline and pathogenesis in Alzheimer's disease. Recent advances in imaging technology enabled generation of high-quality 3D images that can be used to visualize stalled blood vessels. However, localization of stalled vessels in 3D images is often required as the first step for downstream analysis, which can be tedious, time-consuming and error-prone, when done manually. Here, we describe a deep learning-based approach for automatic detection of stalled capillaries in brain images based on 3D convolutional neural networks. Our networks employed custom 3D data augmentations and were used weight transfer from pre-trained 2D models for initialization. We used an ensemble of several 3D models to produce the winning submission to the Clog Loss: Advance Alzheimer's Research with Stall Catchers machine learning competition that challenged the participants with classifying blood vessels in 3D image stacks as stalled or flowing. In this setting, our approach outperformed other methods and demonstrated state-of-the-art results, achieving 0.85 Matthews correlation coefficient, 85% sensitivity, and 99.3% specificity. The source code for our solution is made publicly available.

Tatiana Gabruseva, Dmytro Poplavskiy, Alexandr A. Kalinin

Pneumonia is the leading cause of death among young children and one of the top mortality causes worldwide. The pneumonia detection is usually performed through examine of chest X-ray radiograph by highly-trained specialists. This process is tedious and often leads to a disagreement between radiologists. Computer-aided diagnosis systems showed the potential for improving diagnostic accuracy. In this work, we develop the computational approach for pneumonia regions detection based on single-shot detectors, squeeze-and-excitation deep convolution neural networks, augmentations and multi-task learning. The proposed approach was evaluated in the context of the Radiological Society of North America Pneumonia Detection Challenge, achieving one of the best results in the challenge.

Alexander Rakhlin, Aleksei Tiulpin, Alexey A. Shvets et al.

Breast cancer is one of the main causes of death worldwide. Histopathological cellularity assessment of residual tumors in post-surgical tissues is used to analyze a tumor's response to a therapy. Correct cellularity assessment increases the chances of getting an appropriate treatment and facilitates the patient's survival. In current clinical practice, tumor cellularity is manually estimated by pathologists; this process is tedious and prone to errors or low agreement rates between assessors. In this work, we evaluated three strong novel Deep Learning-based approaches for automatic assessment of tumor cellularity from post-treated breast surgical specimens stained with hematoxylin and eosin. We validated the proposed methods on the BreastPathQ SPIE challenge dataset that consisted of 2395 image patches selected from whole slide images acquired from 64 patients. Compared to expert pathologist scoring, our best performing method yielded the Cohen's kappa coefficient of 0.70 (vs. 0.42 previously known in literature) and the intra-class correlation coefficient of 0.89 (vs. 0.83). Our results suggest that Deep Learning-based methods have a significant potential to alleviate the burden on pathologists, enhance the diagnostic workflow, and, thereby, facilitate better clinical outcomes in breast cancer treatment.

Alexandr A. Kalinin, Gerald A. Higgins, Narathip Reamaroon et al.

This Perspective provides examples of current and future applications of deep learning in pharmacogenomics, including: (1) identification of novel regulatory variants located in noncoding domains and their function as applied to pharmacoepigenomics; (2) patient stratification from medical records; and (3) prediction of drugs, targets, and their interactions. Deep learning encapsulates a family of machine learning algorithms that over the last decade has transformed many important subfields of artificial intelligence (AI) and has demonstrated breakthrough performance improvements on a wide range of tasks in biomedicine. We anticipate that in the future deep learning will be widely used to predict personalized drug response and optimize medication selection and dosing, using knowledge extracted from large and complex molecular, epidemiological, clinical, and demographic datasets.