【24h】

Transillumination Spatially Modulated Illumination Microscopy for Human Chromosome Imaging

机译:用于人体染色体成像的透射照明空间调制照明显微镜

获取原文
获取原文并翻译 | 示例

摘要

Human chromosome analysis is an essential task in cytogenetics, especially in prenatal screening, genetic syndrome diagnosis, cancer pathology research and mutagen dosimetry. Chromosomal analysis begins with the creation of a karyotype, which is a layout of chromosome images organized by decreasing size in pairs. Both manual and automatic classification of chromosomes are limited by the resolution of the microscope and imaging system used. One way to improve the results of classification and even detect subtleties now remaining undetected, is to enhance the resolution of the images. It is possible to achieve lateral resolution beyond the classical limit, by using spatially modulated illumination (SMI) in a wide-field, non-confocal microscope. In this case, the sample is illuminated with spatially modulated light, which makes normally inaccessible high-resolution information visible in the observed image by shifting higher frequencies within the OTF limits of the microscope. Although, SMI microscopes have been reported in the past, this manuscript reports the development of a transillumination microscope for opaque, non-fluorescent samples. The illumination path consisted of a light source illuminating a ruled grating which was subsequently imaged on the sample. The grating was mounted on a rotating and translating stage so that the magnification and rotation of the pattern could be adjusted. The imaging lens was a 1.25 NA oil immersion objective. Test samples showed resolution improvement, as judged from a comparison of the experimentally obtained FWHM. Further studies using smaller fringe distance or laser interference pattern illumination will be evaluated to further optimize the SMI results.
机译:人类染色体分析是细胞遗传学中的一项重要任务,尤其是在产前筛查,遗传综合征诊断,癌症病理学研究和诱变剂量测定中。染色体分析始于核型的创建,核型是通过成对减小大小组织的染色体图像的布局。手动和自动染色体分类都受到所用显微镜和成像系统分辨率的限制。改善分类结果,甚至检测出目前尚未发现的细微之处的一种方法是提高图像的分辨率。通过在宽视场,非凸面显微镜中使用空间调制照明(SMI),可以获得超出经典极限的横向分辨率。在这种情况下,样品将通过空间调制光进行照明,通过在显微镜的OTF限制内移动更高的频率,可以使通常无法访问的高分辨率信息在观察到的图像中可见。尽管过去已经报道过SMI显微镜,但该手稿报道了用于不透明,非荧光样品的透射照明显微镜的发展。照明路径由一个照亮规则光栅的光源组成,该光栅随后成像在样品上。将光栅安装在旋转和平移台上,以便可以调节图案的放大率和旋转度。成像透镜是1.25 NA油浸物镜。根据对实验获得的FWHM的比较判断,测试样品显示出分辨率的提高。将评估使用更小的条纹距离或激光干涉图案照明的进一步研究,以进一步优化SMI结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号