Unlabelled landmark matching via Bayesian data selection, and application to cell matching across imaging modalities

被引:0
|
作者
Forsyth, Jessica E. [1 ,2 ]
Al-Anbaki, Ali H. [2 ]
Plusa, Berenika [2 ]
Cotter, Simon L. [1 ]
机构
[1] Univ Manchester, Dept Math, Manchester M13 9PL, England
[2] Univ Manchester, Fac Biol Med & Hlth, Manchester M13 9PL, England
基金
英国惠康基金;
关键词
Bayesian data selection; Landmark matching; Multi-modal image analysis; INVERSE-WISHART; REGISTRATION; OPTIMIZATION; ALGORITHMS; ALIGNMENT; MATRICES; 2D;
D O I
10.1007/s11222-023-10259-7
中图分类号
TP301 [理论、方法];
学科分类号
081202 ;
摘要
We consider the problem of landmark matching between two unlabelled point sets, in particular where the number of points in each cloud may differ, and where points in each cloud may not have a corresponding match. We invoke a Bayesian framework to identify the transformation of coordinates that maps one cloud to the other, alongside correspondence of the points. This problem necessitates a novel methodology for Bayesian data selection, simultaneous inference of model parameters, and selection of the data which leads to the best fit of the model to the majority of the data. We apply this to a problem in developmental biology where the landmarks correspond to segmented cell centres, where potential death or division of cells can lead to discrepancies between the point-sets from each image. We validate the efficacy of our approach using in silico tests and a microinjected fluorescent marker experiment. Subsequently we apply our approach to the matching of cells between real time imaging and immunostaining experiments, facilitating the combination of single-cell data between imaging modalities. Furthermore our approach to Bayesian data selection is broadly applicable across data science, and has the potential to change the way we think about fitting models to data.
引用
收藏
页数:25
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