Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Science for Life Laboratory, Stockholm, Sweden.
Nat Methods. 2024 Jul;21(7):1245-1256. doi: 10.1038/s41592-024-02294-7. Epub 2024 Jun 6.
Microscopy-based spatially resolved omic methods are transforming the life sciences. However, these methods rely on high numerical aperture objectives and cannot resolve crowded molecular targets, limiting the amount of extractable biological information. To overcome these limitations, here we develop Deconwolf, an open-source, user-friendly software for high-performance deconvolution of widefield fluorescence microscopy images, which efficiently runs on laptop computers. Deconwolf enables accurate quantification of crowded diffraction limited fluorescence dots in DNA and RNA fluorescence in situ hybridization images and allows robust detection of individual transcripts in tissue sections imaged with ×20 air objectives. Deconvolution of in situ spatial transcriptomics images with Deconwolf increased the number of transcripts identified more than threefold, while the application of Deconwolf to images obtained by fluorescence in situ sequencing of barcoded Oligopaint probes drastically improved chromosome tracing. Deconwolf greatly facilitates the use of deconvolution in many bioimaging applications.
基于显微镜的空间分辨组学方法正在改变生命科学。然而,这些方法依赖于高数值孔径物镜,无法解析拥挤的分子靶点,限制了可提取的生物信息量。为了克服这些限制,我们开发了 Deconwolf,这是一个用于宽场荧光显微镜图像的高性能反卷积的开源、用户友好的软件,它可以在笔记本电脑上高效运行。Deconwolf 能够准确量化 DNA 和 RNA 荧光原位杂交图像中拥挤的衍射受限荧光点,并允许对用 ×20 空气物镜成像的组织切片中的单个转录本进行稳健检测。使用 Deconwolf 对原位空间转录组学图像进行反卷积,使鉴定的转录本数量增加了三倍以上,而将 Deconwolf 应用于条形码寡核苷酸探针的荧光原位测序获得的图像,则极大地改善了染色体追踪。Deconwolf 极大地方便了许多生物成像应用中反卷积的使用。