TY - JOUR
T1 - ISegMSI
T2 - An Interactive Strategy to Improve Spatial Segmentation of Mass Spectrometry Imaging Data
AU - Guo, Lei
AU - Liu, Xingxing
AU - Zhao, Chao
AU - Hu, Zhenxing
AU - Xu, Xiangnan
AU - Cheng, Kian Kai
AU - Zhou, Peng
AU - Xiao, Yu
AU - Shah, Mudassir
AU - Xu, Jingjing
AU - Dong, Jiyang
AU - Cai, Zongwei
N1 - The work was supported by the National Natural Science Foundation of China (81871445 and 22176195), the Natural Science Foundation of Fujian province, China (2022Y0003), the Natural Science Foundation of Guangdong Province, China (2021A1515010171), and the Key projects of basic research in Shenzhen (JCYJ20210324115811031). K.K.-C. is supported by a Research University Grant from Universiti Teknologi Malaysia (20H91).
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/10/25
Y1 - 2022/10/25
N2 - Spatial segmentation is a critical procedure in mass spectrometry imaging (MSI)-based biochemical analysis. However, the commonly used unsupervised MSI segmentation methods may lead to inappropriate segmentation results as the MSI data is characterized by high dimensionality and low signal-to-noise ratio. This process can be improved by the incorporation of precise prior knowledge, which is hard to obtain in most cases. In this study, we show that the incorporation of partial or coarse prior knowledge from different sources such as reference images or biological knowledge may also help to improve MSI segmentation results. Here, we propose a novel interactive segmentation strategy for MSI data called iSegMSI, which incorporates prior information in the form of scribble-regularization of the unsupervised model to fine-tune the segmentation results. By using two typical MSI data sets (including a whole-body mouse fetus and human thyroid cancer), the present results demonstrate the effectiveness of the iSegMSI strategy in improving the MSI segmentations. Specifically, the method can be used to subdivide a region into several subregions specified by the user-defined scribbles or to merge several subregions into a single region. Additionally, these fine-tuned results are highly tolerant to the imprecision of the scribbles. Our results suggest that the proposed iSegMSI method may be an effective preprocessing strategy to facilitate the analysis of MSI data.
AB - Spatial segmentation is a critical procedure in mass spectrometry imaging (MSI)-based biochemical analysis. However, the commonly used unsupervised MSI segmentation methods may lead to inappropriate segmentation results as the MSI data is characterized by high dimensionality and low signal-to-noise ratio. This process can be improved by the incorporation of precise prior knowledge, which is hard to obtain in most cases. In this study, we show that the incorporation of partial or coarse prior knowledge from different sources such as reference images or biological knowledge may also help to improve MSI segmentation results. Here, we propose a novel interactive segmentation strategy for MSI data called iSegMSI, which incorporates prior information in the form of scribble-regularization of the unsupervised model to fine-tune the segmentation results. By using two typical MSI data sets (including a whole-body mouse fetus and human thyroid cancer), the present results demonstrate the effectiveness of the iSegMSI strategy in improving the MSI segmentations. Specifically, the method can be used to subdivide a region into several subregions specified by the user-defined scribbles or to merge several subregions into a single region. Additionally, these fine-tuned results are highly tolerant to the imprecision of the scribbles. Our results suggest that the proposed iSegMSI method may be an effective preprocessing strategy to facilitate the analysis of MSI data.
UR - http://www.scopus.com/inward/record.url?scp=85141115886&partnerID=8YFLogxK
U2 - 10.1021/acs.analchem.2c01456
DO - 10.1021/acs.analchem.2c01456
M3 - Journal article
AN - SCOPUS:85141115886
SN - 0003-2700
VL - 94
SP - 14522
EP - 14529
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 42
ER -