CONFOCALMICROSCOPY Archives

January 1997

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Condense Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Content-Type:
TEXT/PLAIN; charset=US-ASCII
Sender:
Confocal Microscopy List <[log in to unmask]>
Subject:
From:
Paul Goodwin <[log in to unmask]>
Date:
Thu, 30 Jan 1997 09:10:21 -0800
In-Reply-To:
MIME-Version:
1.0
Reply-To:
Confocal Microscopy List <[log in to unmask]>
Parts/Attachments:
TEXT/PLAIN (32 lines)
John Cork suggests:

I also have a paper that describes some of these methods and software to
calculate the PSF (Meth. Cell Biol. (40), 221-240).





________________________________________________________________________________


Paul Goodwin
Image Analysis Lab
FHCRC, Seattle, WA

On Thu, 30 Jan 1997 [log in to unmask] wrote:

> Hi.
>
> Everybody is speaking about the PSF...
> Could anyone simply explain how to get this PSF ?
>
>
> ========================    Francois ANGOT    ========================
> [log in to unmask]       http://www.info.unicaen.fr/~fangot
>
> Groupe de Recherches en Informatique, Image et Instrumentation de Caen
>      GREYC-ISMRA - 6 Bd Marechal Juin - 14050 CAEN Cedex - FRANCE
> ======================================================================
>

ATOM RSS1 RSS2