首页> 外文会议>IEEE International Conference on Image Processing >Quantifying Actin Filaments in Microscopic Images using Keypoint Detection Techniques and A Fast Marching Algorithm
【24h】

Quantifying Actin Filaments in Microscopic Images using Keypoint Detection Techniques and A Fast Marching Algorithm

机译:使用关键点检测技术和快速行进算法量化显微图像中的肌动蛋白丝

获取原文

摘要

The actin filament plays a fundamental role in numerous cellular processes such as cell growth, proliferation, migration, division, and locomotion. The actin cytoskeleton is highly dynamical and can polymerize and depolymerize in a very short time under different stimuli. To study the mechanics of actin filament, quantifying the length and number of actin filaments in each time frame of microscopic images is fundamental. In this paper, we adopt a Convolutional Neural Network (CNN) to segment actin filaments first, and then we utilize a modified Resnet to detect junctions and endpoints of filaments. With binary segmentation and detected keypoints, we apply a fast marching algorithm to obtain the number and length of each actin filament in microscopic images. We have also collected a dataset of 10 microscopic images of actin filaments to test our method. Our experiments show that our approach outperforms other existing approaches tackling this problem regarding both accuracy and inference time.
机译:肌动蛋白丝在许多细胞过程中起着基本作用,例如细胞生长,增殖,迁移,分裂和运动。肌动蛋白的细胞骨架是高度动态的,可以在不同的刺激下在很短的时间内聚合和解聚。要研究肌动蛋白丝的力学,量化显微图像每个时间帧中肌动蛋白丝的长度和数量是至关重要的。在本文中,我们采用卷积神经网络(CNN)来分割肌动蛋白丝,然后利用改进的Resnet来检测丝的结点和终点。通过二进制分割和检测到的关键点,我们应用快速行进算法来获取显微图像中每个肌动蛋白丝的数量和长度。我们还收集了肌动蛋白丝的10个显微图像的数据集,以测试我们的方法。我们的实验表明,我们的方法优于其他解决精度和推理时间问题的现有方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号