Location: no longer available
username: immuser
password: !immuser
Brainstorm is a linux PC workstation featuring:
The system has been configured to be straightforward and easy to use.
Deconvolution in Optical Microscopy
“Deconvolution is often suggested as a good alternative to the confocal microscope. Deconvolution is a computationally intensive image processing technique that is being increasingly utilized for improving the contrast and resolution of digital images captured in the microscope. The foundations are based upon a suite of methods that are designed to remove or reverse the blurring present in microscope images induced by the limited aperture of the objective. Nearly any image acquired on a digital fluorescence microscope can be deconvolved.”
Almost any fluorescence microscope can be used with Deconvolution. For example:
There are two ways to access the Brainstorm server in order to use the deconvolution software:
The Huygens Remote Manager is quite simple to use and is quite 'nice' if multiple people are using the system. The idea is that you can add the images you want to deconvolve into a queue and after a few hours they will be deconvolved and ready to download.
Note: will only work inside IMM.
VNC is less friendly but lets you deal with the Huygens software directly. You can access the VNC interface through an internet browser like Internet Explorer
or Mozilla Firefox
. Use the address: http://brainstorm:5801 - will only work inside IMM. Here's a small tutorial.
Note: If you're going to use VNC, do not forget to book the system in the booking system before using it. There can only be one user using the system at a time!
The folder Deconvolution
(visible in the Brainstorm Desktop) is shared in the network (no password or username) in order for you to transfer you files:
Note: For deconvolution with the Huygens Remote Manager
use the folder
brainstorm\deconvolution\HRM\<your_Huygens_Remote_Manager_username>\huygens_src
.
Very important: your data must have almost no saturation!
When you do deconvolution there's some information that you need to know:
Microscope | Objective | NA | Type | Pixel Size |
---|---|---|---|---|
Zeiss Axiovert 200M | 10x | 0.3 | Dry | 983 nm (bin 1) |
Zeiss Axiovert 200M | 20x | 0.5 | Dry | 491 nm (bin 1) |
Zeiss Axiovert 200M | 40x | 0.75 | Dry | 246 nm (bin 1) |
Zeiss Axiovert 200M | 63x | 1.4 | Oil | 156 nm (bin 1) |
Zeiss Axiovert 200M | 100x | 1.4 | Oil | 98 nm (bin 1) |
Zeiss LSM 710 | 10x | 0.3 | Dry | See info below |
Zeiss LSM 710 | 20x | 0.5 | Dry | See info below |
Zeiss LSM 710 | 40x | 1.3 | Oil | See info below |
Zeiss LSM 710 | 63x | 1.4 | Oil | See info below |
Medium | Refraction Index |
---|---|
Air | 1.00 |
Water | 1.33 |
Glycerol + Water | 1.4 |
Halocarbon 400 | 1.412 |
Halocarbon 700 | 1.414 |
Glycerol | 1.456 |
Liquid Vectashield | 1.47 |
Paraffin oil | 1.482 |
m-xylene | 1.497 |
Immersion Oil | 1.515 |
Glass | 1.52 |
Monobromonaphthalene | 1.655 |
Methyl Iodide | 1.76 |
Info
button in the Image Window and a panel should appear, in that panel you have written the pinhole size for each channel.