Bioimaging Wiki

This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong.
{{brainstorm_name.jpg|}}

<html>&nbsp <b>Location</b>: <a href="/facility/bioimaging/lib/exe/fetch.php?media=ubi_map.jpg">Room P3-A-1</a> (<img src="/facility/bioimaging/lib/exe/fetch.php?media=telephone_icon.gif" width=15> 47316)&nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &rarr; <a href="https://imm.medicina.ulisboa.pt/intranet/booking/new/11"><img src="/facility/bioimaging/lib/exe/fetch.php?media=date.png">  Brainstorm Booking</a></html>

{{brainstormscreenshot.png?555}}

**username**: immuser

**password**: !immuser



===== System overview =====
Brainstorm is a linux PC workstation featuring:
  * Huygens Essentials and Huygens Script prepared for Widefield and Confocal deconvolution (blind and non-blind).
  * A dual core 64-bit processor at 2.13GHz
  * 4GB RAM memory
  * Suse 64-bit linux
The system has been configured to be straightforward and easy to use.

{{deconvolutionbycarina.gif?170}}
  - mCherry labeled actin in an Hepatocites (upper part deconvolved, lower part raw data). XYZ 3D reconstruction , Specimen: Carina Santos (2007), Instituto de Medicina Molecular, Lisboa, Portugal.

===== What is Deconvolution? =====
[[http://micro.magnet.fsu.edu/primer/digitalimaging/deconvolution/deconvolutionhome.html|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."

===== Microscopes used with Deconvolution =====
Almost any fluorescence microscope can be used with Deconvolution. For example: 
  * [[zeiss_axiovert_200m|Zeiss Axiovert 200M]]
  * [[zeiss_lsm_710|Zeiss LSM 710]]

===== How to access Brainstorm =====
There are two ways to access the Brainstorm server in order to use the deconvolution software: 
  * Through the [[http://brainstorm/hrm|Huygens Remote Manager]] - the easiest way to do deconvolution, no need to book the system.
  * By Remote Desktop using VNC.


==== Huygens Remote Manager ====
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.

=== To Deconvolve ===
**Note**: will only work inside IMM.
  * Go to [[http://brainstorm/hrm]] and create a user if you don't already have one.
  * Next go to \\brainstorm\deconvolution\HRM\<your username here>\huygens_src and put the data files you want to deconvolve there.
  * Now in [[http://brainstorm/hrm]] after you create your settings you should be able to see your files ready to deconvolve. 
 
==== Remote Desktop using VNC ====
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 [[brainstormvnc|tutorial]].

  * You can also use a vnc client like [[http://www.tightvnc.com|tightvnc]].

**Note**: __If you're going to use VNC, do not forget to book the system in the [[https://imm.medicina.ulisboa.pt/intranet/booking/month.php?user=BRAINSTOR&rid=11|booking system]] before using it. There can only be one user using the system at a time!__

==== Moving files From and To the Brainstorm server ====
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:
   * On windows: go to the //start menu// and select //run//, next enter the text [[\\brainstorm\deconvolution|"\\brainstorm\deconvolution"]] and press __Enter__.
   * On apple mac: in //finder// go to the menu option //go// and //connect to server//, write [[smb://brainstorm/deconvolution|"smb://brainstorm/deconvolution"]]. 

**Note**: For deconvolution with the ''Huygens Remote Manager'' use the folder 
''brainstorm\deconvolution\HRM\<your_Huygens_Remote_Manager_username>\huygens_src''.

==== Deconvolution Tips and Tricks ====
**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  |

=== Pixel (Pinhole) size for Zeiss confocal microscopes ===
  * To get the pinhole size of the [[zeiss_lsm_710|Zeiss LSM 710]] open your image in ZEN 
  * Press the ''Info'' button in the Image Window and a panel should appear, in that panel you have written the pinhole size for each channel.
  * Next go to this [[http://support.svi.nl/wiki/Zeiss_LSM510|link]] to get the pinhole size you should use with Huygens.

===== External links =====
  * [[http://support.svi.nl/wikifiles/hrm_complete.pdf|Huygens Remote Manager: a Web Interface for High-Volume Batch Deconvolution.]] Imaging & Microscopy (2007) V 9, No. 2, pp 57-58.
  * [[http://support.svi.nl/wiki/HuygensEssential|SVI Huygen Essentials wiki]] - tutorials and information

----
[[resources|Back to the Resources page]]
Bioimaging Wiki

User Tools

Site Tools

Page Tools
