Related Experiment Video
Updated: Aug 5, 2026

10:59
Reconstruction of 3-Dimensional Histology Volume and its Application to Study Mouse Mammary Glands
Published on: July 26, 2014
14.5K
End-to-end affine registration framework for histopathological images with weak annotations
Yuanhua Lin1, Zhendong Liang1, Yonghong He1
1Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Computer Methods and Programs in Biomedicine
|August 27, 2023
Summary
ARoNet achieves accurate affine registration for histopathological images, even with large initial rotations. This deep learning framework improves alignment accuracy and speed for digital pathology applications.
Area of Science:
- Digital pathology
- Biomedical image analysis
- Computer vision
Background:
- Histopathological image registration is crucial for digital pathology.
- Existing deep learning methods struggle with large initial rotations in pathology images.
- Accurate initial alignment is vital for effective image registration.
Purpose of the Study:
- To develop a general framework for end-to-end affine registration of histopathological images.
- To address the challenge of large rotation angles in real-world pathology image pairs.
- To improve the accuracy and efficiency of histopathological image registration.
Main Methods:
- ARoNet framework utilizes Convolutional Neural Networks (CNNs) for feature extraction and fusion.
- Incorporates a rotation recognition network to correct significant rotational misalignments.
- Employs a self-supervised learning task for unsupervised image representation learning.
Main Results:
- ARoNet outperforms existing affine registration algorithms in alignment accuracy, especially with large rotations (e.g., 180 degrees).
- Achieves fast execution time (0.05s per pair) with high registration accuracy and robustness.
- Provides accurate affine initialization for subsequent non-rigid alignments.
Conclusions:
- The ARoNet framework simplifies and accelerates histopathological image registration.
- Demonstrates potential for clinical applications in digital pathology.
- Offers a robust solution for handling challenging image misalignments.
More Related Videos
Related Concept Videos
Pedigree Analysis
Overview
DNA Microarrays
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Single Nucleotide Polymorphisms-SNPs
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Epistasis Analysis
Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
Genome-wide Association Studies-GWAS
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
Point and Frameshift Mutations
Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...

