J Chen, H Sasaki, H Lai, Y Su, J Liu, Y Wu, A Zhovmer, C Combs, I Rey-Suarez, H Chang, C Huang, X Li, M Guo, S Nizambad, A Upadhyaya, J Lee, L Lucas, H Shroff.
2/17
We are particularly interested in characterizing the limits of #deeplearning based approaches to image restoration. You will find several experiments comparing several best-in-class approaches: #3DRCAN, #CARE, #SRResNet and #ESRGAN.
Firstly, we looked at how #3DRCAN and other #DL based approaches behave when denoising iSIM images depicting a range of organelles, including: Actin, ER, Golgi, Lysosome, Microtubule, Mitochondria.
We were also interested in finding out the lowest level of illumination (and lowest SNR) for which #3DRCAN could still "work", i.e. create a good quality restoration. Imaging done on an iSIM.
Now that we had nicely restored images (good performance in terms of SSIM and PSNR), we detected and analyzed mitochondria. This was nearly impossible when using the raw/input data.
We then applied the trained #3DRCAN to live cell imaging data (4D). As a result we could study fusion and fission (as imaged by iSIM) events in mitochondria over long time lapses.
Secondly, we wanted to determine if #3DRCAN could be used for other types of super resolution microscopy - we used paired Confocal<->STED 3D data sets to train our models. Imaging done with a Leica SP8. @LeicaMicro
The trained #3DRCAN was applied to raw confocal data (incl. nuclear pores, microtubules and DNA), greatly improving (~2-fold) the spatial resolution. Imaging done with a Leica SP8. @LeicaMicro
Ultimately, we wanted to perform fast 4D confocal imaging and "convert" the raw data to STED-like images. So, we applied the trained #3DRCAN to live cell 3D (confocal) data sets. See 👇
Lastly, we tested whether it was possible to further increase the resolution of iSIM (itself a #superresolution microscopy modality). To do this, we used expansion microscopy to generate the GT we needed to train #3DRCAN for this task.
#3DRCAN was shown to improve both the lateral and axial resolution of iSIM images. Moreover, the improvement in resolution was superior to deconvolving the raw images.
As with the other key experiments, we successfully tested out the trained #3DRCAN on live cell 3D data sets. In this case we imaged mitochondria and microtubules using iSIM.
Disclaimer: this being a twitter thread, a lot of the details are missing - you are most welcome to review the pre-print. Your suggestions and input are welcome.
15/17
You can train your own #3DRCAN models and/or test out the ones we have described here. See github.com/AiviaCommunity… There are also some test images there. Let us know if you have any questions and/or suggestions.
We will start to roll out #AiviaWeb at no cost to use, tomorrow. All #aivia functionality accessible via a web browser. This is part of our #covid19 mitigation plan - more actions soon so you can continue to be productive while #wfh. #bioimageanalyis#aiviacommunity#microscopy
Once you are signed up we will reach out to you with all the details including usage and booking guidelines. A webpage dedicated to our covid19 / wfh mitigation plan will be up very soon too. Many more resources are in the pipeline.
The Seattle metro region and the whole #PNW are being severely affected by the #COVID19outbreak. In >1 month we went from "there is a small cluster of cases in a nursing home" to "we need to lock down the whole region to avoid worst case scenarios" (not happened yet) 1/13
The (social) media frenzy is impressive. Even Facebook and others are worried their servers / data centers may not be able to cope with demand for long (cnn.com/2020/03/18/tec…). We have used social media for good - checking in on friends and family all over the world. 2/13
While this is a challenging time, there are many positive things to be thankful for. Personally, I am enjoying having more time with my young boys (4 and 6 yo) and wife. the boys are curious and scared about the whole story - but 3/13