• 제목/요약/키워드: Cell Image

검색결과 818건 처리시간 0.03초

공초점 레이저 주사 현미경을 이용한 혈구 유동가시화 및 세포공핍층 측정에 관한 연구 (Flow Visualization of Blood Cell and Detection of Cell Depleted Layer Using a Confocal Laser Scanning Microscope)

  • 임수희;김위한;이호;이춘영;박철우
    • 한국가시화정보학회지
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    • 제8권1호
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    • pp.46-52
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    • 2010
  • In the present study, we employed the confocal laser scanning microscopy (CLSM) system to visualize the blood flow field with $1{\times}1{\mu}m^2$ spatial resolution. Based on the confocal microscopic image of red blood cells (RBCs), we performed the velocity vector field measurement and evaluated characteristics of cell migration from the cell depleted layer thickness calculation. The rat and mouse's blood were supplied into a micro glass tubes in vitro. The line scanning rate of confocal microscopy was 15 kHz for a $500{\times}500$ pixels image. As a result, the red blood cell itself can be used as a tracer directly without any kind of invasive tracer particle to get the velocity vector field of blood flow by performing particle image velocimetry (PIV) technique.

마커 제어 워터셰드와 타원 적합기법을 결합한 다중 교모세포종 분할 (Multi-cell Segmentation of Glioblastoma Combining Marker-based Watershed and Elliptic Fitting Method in Fluorescence Microscope Image)

  • 이지영;정다은;이현우;양세정
    • 대한의용생체공학회:의공학회지
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    • 제42권4호
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    • pp.159-166
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    • 2021
  • In order to analyze cell images, accurate segmentation of each cell is indispensable. However, the reality is that accurate cell image segmentation is not easy due to various noises, dense cells, and inconsistent shape of cells. Therefore, in this paper, we propose an algorithm that combines marker-based watershed segmentation and ellipse fitting method for glioblastoma cell segmentation. In the proposed algorithm, in order to solve the over-segmentation problem of the existing watershed method, the marker-based watershed technique is primarily performed through "seeding using local minima". In addition, as a second process, the concave point search using ellipse fitting for final segmentation based on the connection line between the concave points has been performed. To evaluate the performance of the proposed algorithm, we compared three algorithms with other algorithms along with the calculation of segmentation accuracy, and we applied the algorithm to other cell image data to check the generalization and propose a solution.

Digital Gray-Scale/Color Image-Segmentation Architecture for Cell-Network-Based Real-Time Applications

  • Koide, Tetsushi;Morimoto, Takashi;Harada, Youmei;Mattausch, Jurgen Hans
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2002년도 ITC-CSCC -1
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    • pp.670-673
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    • 2002
  • This paper proposes a digital algorithm for gray-scale/color image segmentation of real-time video signals and a cell-network-based implementation architecture in state-of-the-art CMOS technology. Through extrapolation of design and simulation results we predict that about 300$\times$300 pixels can be integrated on a chip at 100nm CMOS technology, realizing very high-speed segmentation at about 1600sec per color image. Consequently real-time color-video segmentation will become possible in near future.

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화상분석기를 이용한 정도별 이형성증에 대한 연구 (The Study of Dysplasic Grades to Digital Image Analyzer)

  • 주경웅
    • 대한임상검사과학회지
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    • 제38권3호
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    • pp.203-207
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    • 2006
  • The purpose of this study was to develop discriminant analysis models for predicting cervical normal/dysplasia case diagnoses using cytometric features derived from the digital image analysis of cell monolayers. The database consisted of 19 cases diagnosed either as normal (n=5), moderate dysplasia (n=7), severe dysplasia (n=7) on monolayer preparations. We studied the nuclear and cytoplasmic characteristics of cells in the normal, moderate dysplasia and severe dysplasia on cervical samples. The morphometric parameters selected for the analysis were nuclear/cytoplasmic ratio and the nuclear variations measured by image analysis on normal and precancerous lesions of cervical smears; several shape factors; area; perimeter; maximal, minimal and equivalent circle diameters. The results showed that the dysplasia samples exhibited changes in both cellular and nuclear form and size but lacked substantial differences in the tumor grades. The coefficient of nuclear variation is as follows to normal cell $21.8{\pm}3.2%$, moderate dysplasia $33.5{\pm}6.1%$, severe dysplasia $27.7{\pm}5.8$ of cervical smears.

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A study of Polarization Modulator to Single-cell type in Polarized Glasses 3D Display System Using Binocular Parallax

  • Kong, Kyung-Bae;Kwon, Jung-Jang
    • 한국컴퓨터정보학회논문지
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    • 제24권11호
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    • pp.71-78
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    • 2019
  • 현재 상용화된 대부분의 3D 디스플레이는 왼쪽 눈과 오른쪽 눈의 입력영상을 다르게 만들어 입체감을 만드는 양안시차 방식을 적용하고 있다. 하지만 상용화된 3D 영상 출력 장치는 성능 부족에 의한 시청자의 불편 유발과 시청위치의 제약 등의 문제들이 있다. 본 논문에서는 기존 Dual-cell 구조 대비 시야각, Crosstalk 감소, 광투과도를 향상할 수 있는 Single-cell 구조의 편광안경식 입체영상 시스템을 개발하고, 투과도 실험과 시야각 평가를 통해 Single-cell 구조의 편광안경식 입체영상 시스템 특성분석과 Dual-cell 구조 대비 성능향상 효과 분석을 진행하였다. 분석 결과 Single-cell 구조가 Dual-cell 구조 대비 투과도 부분에서 약 25% 이상의 높은 성능을 보이며, 시야각 평가 중 입체 영상 특성품질의 주요지표인 3D crosstalk 지표는 약 37% 이상 향상되는 것을 확인할 수 있었다.

디노이징 오토인코더와 그래프 컷을 이용한 딥러닝 기반 바이오-셀 영상 분할 (Bio-Cell Image Segmentation based on Deep Learning using Denoising Autoencoder and Graph Cuts)

  • 임선자;칼렙부누누;권오흠;이석환;권기룡
    • 한국멀티미디어학회논문지
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    • 제24권10호
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    • pp.1326-1335
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    • 2021
  • As part of the cell division method, we proposed a method for segmenting images generated by topography microscopes through deep learning-based feature generation and graph segmentation. Hybrid vector shapes preserve the overall shape and boundary information of cells, so most cell shapes can be captured without any post-processing burden. NIH-3T3 and Hela-S3 cells have satisfactory results in cell description preservation. Compared to other deep learning methods, the proposed cell image segmentation method does not require postprocessing. It is also effective in preserving the overall morphology of cells and has shown better results in terms of cell boundary preservation.

A Study on an Automatic Multi-Focus System for Cell Observation

  • Park, Jaeyoung;Lee, Sangjoon
    • Journal of Information Processing Systems
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    • 제15권1호
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    • pp.47-54
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    • 2019
  • This study is concerned with the mechanism and structure of an optical microscope and an automatic multi-focus algorithm for automatically selecting sharp images from multiple foci of a cell. To obtain precise cell images quickly, a z-axis actuator with a resolution of $0.1{\mu}m$ was designed to control an optical microscope Moreover, a lighting control system was constructed to select the color and brightness of light that best suit the object being viewed. Cell images are captured by the instrument and the sharpness of each image is determined using Gaussian and Laplacian filters. Next, cubic spline interpolation and peak detection algorithms are applied to automatically find the most vivid points among multiple images of a single object. A cancer cell imaging experiment using propidium iodide staining confirmed that a sharp multipoint image can be obtained using this microscope. The proposed system is expected to save time and effort required to extract suitable cell images and increase the convenience of cell analysis.

Quantitative Image Analysis of Fluorescence Image Stacks: Application to Cytoskeletal Proteins Organization in Tissue Engineering Constructs

  • Park, Doyoung
    • 한국정보기술학회 영문논문지
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    • 제9권1호
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    • pp.103-113
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    • 2019
  • Motivation: Polymerized actin-based cytoskeletal structures are crucial in shape, dynamics, and resilience of a cell. For example, dynamical actin-containing ruffles are located at leading edges of cells and have a significant impact on cell motility. Other filamentous actin (F-actin) bundles, called stress fibers, are essential in cell attachment and detachment. For this reason, their mechanistic understanding provides crucial information to solve practical problems related to cell interactions with materials in tissue engineering. Detecting and counting actin-based structures in a cellular ensemble is a fundamental first step. In this research, we suggest a new method to characterize F-actin wrapping fibers from confocal fluorescence image stacks. As fluorescently labeled F-actin often envelope the fibers, we first propose to segment these fibers by diminishing an energy based on maximum flow and minimum cut algorithm. The actual actin is detected through the use of bilateral filtering followed by a thresholding step. Later, concave actin bundles are detected through a graph-based procedure that actually determines if the considered actin filament is enclosing the fiber.

전반사 형광 이미지 분석을 통한 세포 부착점의 운동 특성에 관한 연구 (On the Dynamic Characteristics of Cell Contact by Analyzing TIRE Images)

  • 이용구;진송완;구상모;유정열
    • 대한기계학회논문집A
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    • 제31권3호
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    • pp.380-387
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    • 2007
  • We carried out an image analysis of living cells forming their contacts at the bottom of the cell culturing substrate. In order to visualize the contact area selectively, we adopted total-internal-reflection-fluorescence (TIRF) method, which can illuminate the specimen volume within only several hundred nano-meters above the substrate. From the fluorescent intensity of the TRF image, we could calculate the distance of the cell surface from the substrate. As a result, we visualized the origin of cell contacts, their movements, and the change of cell-contact type from the close-contact into focal-contact with information of its vertical displacement representing the temporal evolution process of the three-dimensional cell-surface-profile near the contact area during this metamorphosis.