PO.BCS01.13 · 生物信息与计算
ecSegCls:基于深度学习的方法用于在间期和中期癌细胞中检测染色体外DNA
ecSegCls: Deep learning-based method for detecting extrachromosomal DNAs in both interphase and metaphase cancer cells
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
染色体外DNA(ecDNA)是一种无着丝粒的环状DNA元件,源自染色体但独立于染色体存在。ecDNA常携带高拷贝数的癌基因,导致肿瘤异质性和患者预后不良。全基因组测序提供全基因组范围的ecDNA检测,但缺乏空间分辨率,而荧光原位杂交(FISH)等成像方法可捕获空间背景,但依赖专家进行劳动密集型的手动标注。现有的用于从FISH自动检测ecDNA的工具(如ecSeg)部分解决了这一局限,但仍局限于中期细胞,且分类性能一般。在此,我们提出ecSegCls,这是一个用于在FISH和DAPI图像中高精度分割和分类ecDNA的自动化流程。我们提出的方法既利用基于深度学习的分割模型及其提取的特征,也利用基于XGBoost的分类模型,从而形成分割细胞核、染色体和ecDNA区域并预测中期和间期细胞中ecDNA存在的流程。数据增强和噪声模拟被用于提高稳健性,分割衍生的特征被用于训练XGBoost分类器。消融研究进一步识别了关键的预测特征,增强了可解释性。我们使用来自癌细胞系的483张FISH图像的公共数据集作为模型训练集,以及内部生成的来自8个癌细胞系的776张FISH图像的数据集作为分类集,评估并比较了我们的模型与先前发表架构的性能,包括UNet、UNet++、DeepLabV3+、Swin UNet、FATNet、HiFormer、DAEFormer和ecSeg。我们提出的ecSegCls取得了卓越的定性和定量性能,在分割和分类基准测试中于多样区域和多种指标上均产生高性能,从而确立了ecSegCls作为一个稳健且可扩展的自动化框架用于准确检测ecDNA,推进基于成像的ecDNA研究和临床应用。
查看英文原文 English abstract
Extrachromosomal DNA (ecDNA) is an acentric circular DNA element that derives from but exists independently of chromosomes. EcDNAs often carry oncogenes with high copy numbers, contributing to tumor heterogeneity, and poor patient outcomes. Whole genome sequencing provides genome-wide detection of ecDNAs but lacks spatial resolution, while imaging methods such as fluorescence in situ hybridization (FISH) capture spatial context but rely on labor-intensive manual annotation by experts. Existing tools for automated detection of ecDNAs from FISH, such as ecSeg, partially address this limitation but remain restricted to metaphase cells, demonstrating modest classification performance. Here, we present ecSegCls, an automated pipeline for segmenting and classifying ecDNA in FISH and DAPI images with high accuracy. Our proposed method exploits both deep learning-based segmentation model and its extracted features, as well as XGBoost-based classification model, leading to the pipeline of segmenting nuclei, chromosomes, and ecDNA regions, and predicting the presence of ecDNA in both metaphase and interphase cells. Data augmentation and noise simulation were used for improved robustness and segmentation-derived features were used for training an XGBoost classifier. Ablation studies further identified key predictive features, enhancing interpretability. Using a public dataset of 483 FISH images from cancer cell lines as a model training set and a dataset of 776 FISH images internally generated 8 cancer cell lines as a classification set, we assessed and compared the performance of our model with those of previously published architectures, including UNet, UNet++, DeepLabV3+, Swin UNet, FATNet, HiFormer, DAEFormer, and ecSeg. Our proposed ecSegCls has achieved remarkable qualitative and quantitative performance, yielding high performance on diverse regions with diverse metrics in both segmentation and classification benchmarks, thus establishing ecSegCls as a robust and scalable automated framework for accurate ecDNA detection, advancing imaging-based research and clinical applications with ecDNA.
利益披露 Disclosure
S. Chun, None..
H. Seo, None..
Y. Nam, None..
D. Kang, None..
H. Bae, None..
R. Lee, None..
H. Kim, None.