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Khurana, Y.

Publications and source records attributed to Khurana, Y..

3 recordsLinked to original sources

pykarambola: Minkowski tensor morphometry of 3D structures

Three-dimensional biological morphologies encode functional and physiological state, yet the directional, orientational, and topological properties of these shapes are rarely captured by morphometric tools available for bioimage analysis. Minkowski tensors are mathematically rigorous tensor-valued measures that encode surface curvature and directionality for objects of arbitrary topology, with tensor eigensystems that directly quantify elongation axes and anisotropy. A C++ implementation, karambola (1), computes Minkowski tensors for triangulated surfaces but is inaccessible within Python-based bioimage workflows. Here we present pykarambola, a pip installable Python package that accepts NumPy arrays and standard mesh formats and returns Minkowski tensors, including derived anisotropy and orientation quantities. A high-level label-image API converts 3D integer arrays into per-object Minkowski tensors in a single call, making pykarambola directly compatible with the output of widely used segmentation tools. An optional Cython extension accelerates graph-traversal steps of mesh initialization for large-scale analyses. Benchmarked on 1,584 adrenal gland meshes, pykarambola reproduces all 121 C++ karambola output features to near-floating-point agreement and, in the pure-Python build, is 2.8x faster at 283 and 1.5x faster at 643 voxel resolution, with speedups primarily attributable to karambolas sequential per-object file I/O. pykarambola is freely available as an open-source software package.

bioinformatics↗

Hyaluronan underlies the emergence of form, fate, and function in human cardioids

The extracellular matrix (ECM) is crucial for organ development and disease. Yet, the interplay among cells, function, and the ECM during human cardiogenesis remains obscure. Using human cardioids, we discovered that cardiac mesoderm-synthesized hyaluronan (HA) underlies early cardiac functional development. HA drives cardioid cavity formation through hydrogel swelling and bioscaffolding, critical functions of the cardiac jelly in the early vertebrate heart. During an early developmental window, HA is essential for establishing cardiac cell identity, while at later stages, HA-generated forces promote beating function through mechanosensitive channels. Chamber-specific differences in mechanical sensitivity ensure robust contractions in multi-chambered tissues. Our findings reveal how a single endogenous ECM component orchestrates the co-emergence of form, fate, and function during human organogenesis, opening new avenues for bioengineering physiologically relevant organ models.

developmental biology↗

LivecellX: A Deep-learning-based, Single-Cell Object-Oriented Framework for Quantitative Analysis in Live-Cell Imaging

Live-cell imaging uniquely captures single-cell dynamics in space and time, but robust analysis is limited by segmentation and tracking errors that accumulate across frames. We present LivecellX, a deep-learning-based pipeline that integrates instance-level segmentation error correction with trajectory refinement, leveraging temporal context to recover accurate cell tracks. LivecellX also introduces a benchmark dataset with detailed annotations of common error classes, providing a resource for method development and evaluation. Beyond error correction, the framework incorporates modules for classifying biological processes, reconstructing cell lineages, and analyzing dynamic behaviors. Users can interact with the system programmatically or through a Napari-based graphical interface, enabling flexible integration into diverse workflows. By coupling error-aware correction with comprehensive lineage and dynamics analysis, LivecellX establishes an open, extensible platform that advances the accuracy and scalability of live-cell imaging studies.

biophysics↗