{"title":"基于纹理的模式识别从相衬图像实现干细胞的动态形态学表征","authors":"M. Maddah, K. Loewke","doi":"10.1109/ISBI.2014.6867813","DOIUrl":null,"url":null,"abstract":"The increased use of stem cells to study disease states in vitro has created a need for tools that provide automated, non-invasive, and objective characterization of cell cultures. In this work, we address this need by developing a novel framework for stem cell assessment using time-lapse phase-contrast microscopy and automated texture-based analysis of images. We capture and quantify morphological changes during stem cell colony growth by segmenting each image of the time-lapse sequence into five distinct classes of cells. We apply our automated classification to enable non-invasive estimation of cell doubling time, and demonstrate applications of the presented framework for quantitative assessment of cell culture conditions.","PeriodicalId":440405,"journal":{"name":"2014 IEEE 11th International Symposium on Biomedical Imaging (ISBI)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Dynamic morphology-based characterization of stem cells enabled by texture-based pattern recognition from phase-contrast images\",\"authors\":\"M. Maddah, K. Loewke\",\"doi\":\"10.1109/ISBI.2014.6867813\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The increased use of stem cells to study disease states in vitro has created a need for tools that provide automated, non-invasive, and objective characterization of cell cultures. In this work, we address this need by developing a novel framework for stem cell assessment using time-lapse phase-contrast microscopy and automated texture-based analysis of images. We capture and quantify morphological changes during stem cell colony growth by segmenting each image of the time-lapse sequence into five distinct classes of cells. We apply our automated classification to enable non-invasive estimation of cell doubling time, and demonstrate applications of the presented framework for quantitative assessment of cell culture conditions.\",\"PeriodicalId\":440405,\"journal\":{\"name\":\"2014 IEEE 11th International Symposium on Biomedical Imaging (ISBI)\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2014 IEEE 11th International Symposium on Biomedical Imaging (ISBI)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ISBI.2014.6867813\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2014 IEEE 11th International Symposium on Biomedical Imaging (ISBI)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ISBI.2014.6867813","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Dynamic morphology-based characterization of stem cells enabled by texture-based pattern recognition from phase-contrast images
The increased use of stem cells to study disease states in vitro has created a need for tools that provide automated, non-invasive, and objective characterization of cell cultures. In this work, we address this need by developing a novel framework for stem cell assessment using time-lapse phase-contrast microscopy and automated texture-based analysis of images. We capture and quantify morphological changes during stem cell colony growth by segmenting each image of the time-lapse sequence into five distinct classes of cells. We apply our automated classification to enable non-invasive estimation of cell doubling time, and demonstrate applications of the presented framework for quantitative assessment of cell culture conditions.