arXiv subjects

Christine Mac Donald

Publications and source records attributed to Christine Mac Donald.

3 recordsLinked to original sources

arXiv2025

Reference-Free 3D Reconstruction of Brain Dissection Slabs via Learned Atlas Coordinates

Correlation of neuropathology with MRI has the potential to transfer microscopic signatures of pathology to in vivo scans. There is increasing interest in building these correlations from 3D reconstructed stacks of slab photographs, which are routinely taken during dissection at brain banks. These photographs bypass the need for ex vivo MRI, which is not widely accessible. However, existing methods either require a corresponding 3D reference (e.g., an ex vivo MRI scans, or a brain surface acquired with a structured light scanner) or a full stack of brain slabs, which severely limits applicability. Here we propose RefFree, a 3D reconstruction method for dissection photographs that does not require an external reference. RefFree coherently reconstructs a 3D volume for an arbitrary set of slabs (including a single slab) using predicted 3D coordinates in the standard atlas space (MNI) as guidance. To support RefFree's pipeline, we train an atlas coordinate prediction network that estimates the coordinate map from a 2D photograph, using synthetic photographs generated from digitally sliced 3D MRI data with randomized appearance for enhanced generalization. As a by-product, RefFree can propagate information (e.g., anatomical labels) from atlas space to one single photograph even without reconstruction. Experiments on simulated and real data show that, when all slabs are available, RefFree achieves performance comparable to existing classical methods but at substantially higher speed. Moreover, RefFree yields accurate reconstruction and registration for partial stacks or even a single slab. Our code is available at https://github.com/lintian-a/reffree.

eess.IV↗

arXiv2020

3D Reconstruction and Segmentation of Dissection Photographs for MRI-free Neuropathology

Neuroimaging to neuropathology correlation (NTNC) promises to enable the transfer of microscopic signatures of pathology to in vivo imaging with MRI, ultimately enhancing clinical care. NTNC traditionally requires a volumetric MRI scan, acquired either ex vivo or a short time prior to death. Unfortunately, ex vivo MRI is difficult and costly, and recent premortem scans of sufficient quality are seldom available. To bridge this gap, we present methodology to 3D reconstruct and segment full brain image volumes from brain dissection photographs, which are routinely acquired at many brain banks and neuropathology departments. The 3D reconstruction is achieved via a joint registration framework, which uses a reference volume other than MRI. This volume may represent either the sample at hand (e.g., a surface 3D scan) or the general population (a probabilistic atlas). In addition, we present a Bayesian method to segment the 3D reconstructed photographic volumes into 36 neuroanatomical structures, which is robust to nonuniform brightness within and across photographs. We evaluate our methods on a dataset with 24 brains, using Dice scores and volume correlations. The results show that dissection photography is a valid replacement for ex vivo MRI in many volumetric analyses, opening an avenue for MRI-free NTNC, including retrospective data. The code is available at https://github.com/htregidgo/DissectionPhotoVolumes.

cs.CV↗

arXiv2019

Network Differential Connectivity Analysis

Identifying differences in networks has become a canonical problem in many biological applications. Here, we focus on testing whether two Gaussian graphical models are the same. Existing methods try to accomplish this goal by either directly comparing their estimated structures, or testing the null hypothesis that the partial correlation matrices are equal. However, estimation approaches do not provide measures of uncertainty, e.g., $p$-values, which are crucial in drawing scientific conclusions. On the other hand, existing testing approaches could lead to misleading results in some cases. To address these shortcomings, we propose a qualitative hypothesis testing framework, which tests whether the connectivity patterns in the two networks are the same. Our framework is especially appropriate if the goal is to identify nodes or edges that are differentially connected. No existing approach could test such hypotheses and provide corresponding measures of uncertainty, e.g., $p$-values. We investigate theoretical and numerical properties of our proposal and illustrate its utility in biological applications. Theoretically, we show that under appropriate conditions, our proposal correctly controls the type-I error rate in testing the qualitative hypothesis. Empirically, we demonstrate the performance of our proposal using simulation datasets and applications in cancer genetics and brain imaging studies.

stat.ME↗