Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
You are invited to
attend a live, interactive, web-based instructional seminar:
==============================================================
"Deconvolution - Issues to Consider for Widefield and
Confocal Microscopy"
Presented by Jonathan
Girrior
3D Applications Manager
at AutoQuant Imaging (now part of Media
Cybernetics)
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Details are
below. Connection lines are limited, so reserve yours now. There is no charge to
participate in this on-line seminar.
When:
Thursday, 27-September, 1:00PM (Eastern time; 10 AM Pacific time.)
Details:
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Deconvolution has proven to be a powerful
new tool for performing high-resolution multi-dimensional imaging of
biological specimens. It is used for increasing the sensitivity and
improving the resolution of standard widefield microscopes and for improving the
resolving capabilities of confocal systems. Attendees of this live, no-cost webinar will
learn about the latest technology for
performing deconvolution on a variety of microscope images and understand
better the relative strengths and weaknesses of several popular
algorithms. Bring your questions to this
live, interactive web-based seminar.
- What is
deconvolution and how does it
work?
- Discussion on empirical vs. derived point-spread
functions
- Uses in fluorescence and brightfield
modalities
- Difference from confocal imaging
- How do I choose
one over the other?
- Pro and cons-
where deconvolution works and where it
doesn't
- Challenges and advice
- A few before/after
examples using Image Pro 3D
Constructor
Upcoming Webinar: "3D Imaging: Issues to Consider for Biological
Microscopy" (invitations will be sent
separately).
This seminar requires
that attendees use a Java-enabled browser with a high bandwidth connection. Audio is via toll-free
telephone.
There is no charge to participate in this on-line
seminar.
Locked
