| Literature DB >> 33283212 |
Donglai Wei1, Zudi Lin1, Daniel Franco-Barranco2,3, Nils Wendt4, Xingyu Liu5, Wenjie Yin1, Xin Huang6, Aarush Gupta7, Won-Dong Jang1, Xueying Wang1, Ignacio Arganda-Carreras2,3,8, Jeff W Lichtman1, Hanspeter Pfister1.
Abstract
Electron microscopy (EM) allows the identification of intracellular organelles such as mitochondria, providing insights for clinical and scientific studies. However, public mitochondria segmentation datasets only contain hundreds of instances with simple shapes. It is unclear if existing methods achieving human-level accuracy on these small datasets are robust in practice. To this end, we introduce the MitoEM dataset, a 3D mitochondria instance segmentation dataset with two (30μm)3 volumes from human and rat cortices respectively, 3, 600× larger than previous benchmarks. With around 40K instances, we find a great diversity of mitochondria in terms of shape and density. For evaluation, we tailor the implementation of the average precision (AP) metric for 3D data with a 45× speedup. On MitoEM, we find existing instance segmentation methods often fail to correctly segment mitochondria with complex shapes or close contacts with other instances. Thus, our MitoEM dataset poses new challenges to the field. We release our code and data: https://donglaiw.github.io/page/mitoEM/index.html.Entities:
Keywords: 3D Instance Segmentation; EM Dataset; Mitochondria
Year: 2020 PMID: 33283212 PMCID: PMC7713709 DOI: 10.1007/978-3-030-59722-1_7
Source DB: PubMed Journal: Med Image Comput Comput Assist Interv