A novel registration method for long-serial section images of EM with a serial split technique based on unsupervised optical flow network.

IF 4.4 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Bioinformatics Pub Date : 2023-08-01 DOI:10.1093/bioinformatics/btad436
Tong Xin, Yanan Lv, Haoran Chen, Linlin Li, Lijun Shen, Guangcun Shan, Xi Chen, Hua Han
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Abstract

Motivation: The registration of serial section electron microscope images is a critical step in reconstructing biological tissue volumes, and it aims to eliminate complex nonlinear deformations from sectioning and replicate the correct neurite structure. However, due to the inherent properties of biological structures and the challenges posed by section preparation of biological tissues, achieving an accurate registration of serial sections remains a significant challenge. Conventional nonlinear registration techniques, which are effective in eliminating nonlinear deformation, can also eliminate the natural morphological variation of neurites across sections. Additionally, accumulation of registration errors alters the neurite structure.

Results: This article proposes a novel method for serial section registration that utilizes an unsupervised optical flow network to measure feature similarity rather than pixel similarity to eliminate nonlinear deformation and achieve pairwise registration between sections. The optical flow network is then employed to estimate and compensate for cumulative registration error, thereby allowing for the reconstruction of the structure of biological tissues. Based on the novel serial section registration method, a serial split technique is proposed for long-serial sections. Experimental results demonstrate that the state-of-the-art method proposed here effectively improves the spatial continuity of serial sections, leading to more accurate registration and improved reconstruction of the structure of biological tissues.

Availability and implementation: The source code and data are available at https://github.com/TongXin-CASIA/EFSR.

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一种基于无监督光流网络的EM长序列切片图像序列分割配准方法。
动机:连续切片电镜图像的配准是重建生物组织体积的关键步骤,其目的是消除切片中复杂的非线性变形,复制正确的神经突结构。然而,由于生物结构的固有特性和生物组织切片制备带来的挑战,实现序列切片的准确注册仍然是一个重大挑战。传统的非线性配准技术可以有效地消除非线性变形,但也可以消除神经突横断面的自然形态变化。此外,配准误差的累积会改变神经突的结构。结果:本文提出了一种新的连续截面配准方法,该方法利用无监督光流网络测量特征相似度,而不是像素相似度,以消除非线性变形,实现截面间的两两配准。然后使用光流网络来估计和补偿累积配准误差,从而允许重建生物组织的结构。基于新颖的序列切片配准方法,提出了一种长序列切片的序列分割技术。实验结果表明,本文提出的方法有效地提高了序列切片的空间连续性,从而提高了生物组织结构的配准精度和重建效果。可用性和实现:源代码和数据可在https://github.com/TongXin-CASIA/EFSR上获得。
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来源期刊
Bioinformatics
Bioinformatics 生物-生化研究方法
CiteScore
11.20
自引率
5.20%
发文量
753
审稿时长
2.1 months
期刊介绍: The leading journal in its field, Bioinformatics publishes the highest quality scientific papers and review articles of interest to academic and industrial researchers. Its main focus is on new developments in genome bioinformatics and computational biology. Two distinct sections within the journal - Discovery Notes and Application Notes- focus on shorter papers; the former reporting biologically interesting discoveries using computational methods, the latter exploring the applications used for experiments.
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