linear unmixing

[Vergara, Leoncio A.]

Dear List contributors

 

I am using the spectral imaging capabilities of a Zeiss LSM510 META
Confocal microscope. I have used in the past a pluggin to read .lsm
files into Image J for analysis. I was wondering if there are any
resources to perform linear unmixing analysis of the Zeiss generated
data? I have the lambda scans of the samples and spectral reference
controls. I would appreciate your help. Thanks in advance

 

Leoncio

 

Leoncio A. Vergara MD

Assistant Professor
Laboratory of Protein Misfolding Diseases (lab-PMD),
George and Cynthia Mitchell Center for Neurodegenerative Diseases
Research.

Director of the Optical Imaging Lab. (OIL),

Dept. of Neuroscience and Cell Biology

University of Texas Medical Branch (UTMB)

301 University Blvd

Galveston, Texas 77555-0641

OIL phone: [phone]  

Lab-PMD phone: [phone]

fax: [phone]