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Alexey Ershov

Publications and source records attributed to Alexey Ershov.

3 recordsLinked to original sources

Self-Supervised Learning for Biological Sample Localization in 3D Tomographic Images

In synchrotron-based Computed Tomography (CT) there is a trade-off between spatial resolution, field of view and speed of positioning and alignment of samples. The problem is even more prominent for high-throughput tomography--an automated setup, capable of scanning large batches of samples without human interaction. As a result, in many applications, only 20-30% of the reconstructed volume contains the actual sample. Such data redundancy clutters the storage and increases processing time. Hence, an automated sample localization becomes an important practical problem. In this work, we describe two self-supervised losses designed for biological CT. We further demonstrate how to employ the uncertainty estimation for sample localization. This approach shows the ability to localize a sample with less than 1.5\% relative error and reduce the used storage by a factor of four. We also show that one of the proposed losses works reasonably well as a pre-training task for the semantic segmentation.

cs.CV

Using the Order of Tomographic Slices as a Prior for Neural Networks Pre-Training

The technical advances in Computed Tomography (CT) allow to obtain immense amounts of 3D data. For such datasets it is very costly and time-consuming to obtain the accurate 3D segmentation markup to train neural networks. The annotation is typically done for a limited number of 2D slices, followed by an interpolation. In this work, we propose a pre-training method SortingLoss. It performs pre-training on slices instead of volumes, so that a model could be fine-tuned on a sparse set of slices, without the interpolation step. Unlike general methods (e.g. SimCLR or Barlow Twins), the task specific methods (e.g. Transferable Visual Words) trade broad applicability for quality benefits by imposing stronger assumptions on the input data. We propose a relatively mild assumption -- if we take several slices along some axis of a volume, structure of the sample presented on those slices, should give a strong clue to reconstruct the correct order of those slices along the axis. Many biomedical datasets fulfill this requirement due to the specific anatomy of a sample and pre-defined alignment of the imaging setup. We examine the proposed method on two datasets: medical CT of lungs affected by COVID-19 disease, and high-resolution synchrotron-based full-body CT of model organisms (Medaka fish). We show that the proposed method performs on par with SimCLR, while working 2x faster and requiring 1.5x less memory. In addition, we present the benefits in terms of practical scenarios, especially the applicability to the pre-training of large models and the ability to localize samples within volumes in an unsupervised setup.

eess.IV

Megahertz X-ray microscopy at X-ray Free-Electron Laser and Synchrotron sources

We demonstrate X-ray phase contrast microscopy performed at the European X-ray Free-Electron Laser sampled at 1.128 MHz rate. We have applied this method to image stochastic processes induced by an optical laser incident on water-filled capillaries with micrometer scale spatial resolution. The generated high speed water jet, cavitation formation and annihilation in water and glass, as well as glass explosions are observed. The comparison between XFEL and previous synchrotron MHz microscopy shows the superior contrast and spatial resolution at the XFEL over the synchrotron. This work opens up new possibilities for the characterization of dynamic stochastic systems on nanosecond to microsecond time scales at megahertz rate with object velocities up to few kilometers per second using X-ray Free-Electron Laser sources.

physics.ins-det