Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.10.17.759823

Robust geometric drift correction and identity reconstruction for biological 3D time-lapse point clouds

Abstract

Structural time-lapse microscopy experiments aim to follow cells or subcellular structures over time, typically by detecting objects in each frame and linking them into trajectories. In practice, this process yields sequences of spatial coordinates derived from segmentation, while identity information across time is often absent or unreliable. In addition, the observed coordinates may be affected by systematic geometric drift. As a result, two coupled inference problems arise: geometric drift must be corrected, and object identities must be reconstructed from unlabeled point clouds. Here, we formulate both drift correction and identity reconstruction within a unified point-cloud framework and evaluate them jointly using controlled synthetic benchmarks and biological datasets. For drift correction, we compare rigid, local, and nonparametric models across spatially varying and non-rigid drift regimes. For identity reconstruction, we analyze a family of Hungarian assignment methods with constant-velocity refinement and different gating strategies, including innovation-based normalization. Across benchmarks, we find that increased model flexibility does not necessarily improve drift correction. A simple rigid stepwise model provides the most robust performance across a wide range of conditions, with a local community model as a competitive alternative under structured spatial heterogeneity. On the association side, innovation-based gating emerges as the key determinant of performance. Hungarian constant-velocity assignment with normalized innovation gating consistently outperforms coordinate-space variants, particularly under heterogeneous motion scales, birth and death processes, and density-induced ambiguity. Application to biological datasets confirms that the combined pipeline improves trajectory consistency and restores interpretable motion statistics, while highlighting the role of proxy references when ground truth is unavailable. Together, these results establish a practical and robust workflow for post hoc trajectory analysis in point-cloud-based time-lapse data, and clarify the methodological trade-offs between model expressivity and robustness in both drift correction and identity reconstruction.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Musacchio, F., Fuhrmann, M.. 2026-10-19. Robust geometric drift correction and identity reconstruction for biological 3D time-lapse point clouds. https://doi.org/10.64898/2026.10.17.759823

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Carrier-Limited Release Risk in Electrospun Nanofibers for Regenerative Endodontics: Constraint Discovery from 25 Formulations

Regenerative endodontics needs an intracanal carrier that keeps disinfecting across a dressing interval that clinicians schedule at one to four weeks, without harming the stem cells that rebuild the pulp. We ask what one completed 25-formulation electrospinning campaign of poly(vinylpyrrolidone) (PVP) fibers carrying metronidazole, ciprofloxacin, minocycline and Ca(OH)2 can decide, and use machine learning for constraint discovery and decision support rather than as a new predictor. After an audit against the source thesis, logistic regression predicts fine-fiber formation at 96% leave-one-out accuracy, but a one-threshold rule does as well, the gain over the 80% majority baseline is not significant (exact McNemar p = 0.125), and accuracy falls to 84% when mixture loading is encoded per component. Diameter models interpolate within formulation families (ridge MAE 193 nm, 95% CI 96 to 317 nm) and fail across them (R^2 < 0). Because the campaign never measured release, we assemble a same-drug, cross-carrier evidence table: 17 bounded metronidazole and ciprofloxacin observations from seven studies, with two-sided censoring. Water-soluble carriers (PVP, PVA) completed release within 80 h (PVP within 8 h); no water-insoluble monolithic carrier reached 90% within its observation window, releasing 1.5 to 50%; both within-study comparisons separate at matched loading; and blend, core-shell and thick-mat architectures released over 3 to 28 days. The PVP mats therefore carry a carrier-limited release risk, not a proven ceiling, and one dissolution experiment can confirm or overturn it. A censoring-aware screen keeps three necessarily and one possibly nondominated formulation, and fixed-budget replays show that uncertainty sampling finds failed formulations sooner, except the one it is confidently wrong about.

bioinformatics↗

CellMethMarker provides an integrated database of human cell- and tissue-type-specific DNA methylation markers

Cell- and tissue-type-specific DNA methylation markers provide epigenetic signatures of cellular identity and are widely used to infer cellular origin from bulk and single-cell methylomes. Existing resources mainly emphasize disease-associated biomarkers, methylome atlases, genomic annotations or RNA-based cell markers, leaving an unmet need for an integrated region-level resource dedicated to such markers. Here we present CellMethMarker (http://gu-zhanglab.hfcas.ac.cn/CellMethMarker), a curated database integrating 347,514 de novo markers derived from uniformly processed whole-genome and reduced-representation bisulfite sequencing datasets, 2,203,507 literature-derived marker records and harmonized metadata for 2,810 samples. CellMethMarker enables cell- and tissue-centered marker retrieval, coordinate-based search, genome-browser visualization, interactive methylation analysis and data download. In an independent single-cell methylome atlas, these markers recover the expected cell-type-associated methylation patterns, and a platform-matched reference built from them lowers the mean deconvolution error from 0.365 to 0.144. CellMethMarker therefore links region-level DNA methylation variation to cellular identity and supports methylome-based cell-type annotation and deconvolution.

bioinformatics↗

IG-28 enables identification and quantification of high-confidence isoforms from large bulk and single-cell full-length cDNA datasets

The technology to sequence full-length transcriptomes from bulk and single-cell samples has rapidly advanced. As a result, full-length cDNA datasets now reach billions of reads in size which is beyond the capability of most established isoform identification tools. Here, we introduce IG-28 which addresses this challenge with its capability to process and analyze large fl-cDNA datasets fast and using minimal computational resources. In contrast to its predecessor Mandalorion, IG-28 is not limited to bulk fl-cDNA but is capable of parsing, processing, and analyzing single-cell fl-cDNA datasets. It does so in a lightweight, flexible manner, integrating seamlessly with established scRNA-seq analysis workflows. We benchmarked IG-28 against a variety of established and new isoform identification tools using several bulk and a complex single-cell fl-cDNA dataset and found that IG-28 consistently outperformed the other tools by identifying high-confidence public isoforms.

bioinformatics↗