CONFOCALMICROSCOPY Archives

March 2008

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
Sender:
Confocal Microscopy List <[log in to unmask]>
Date:
Wed, 12 Mar 2008 11:17:31 +0200
Reply-To:
Subject:
MIME-Version:
1.0
Content-Transfer-Encoding:
7bit
In-Reply-To:
Content-Type:
text/plain; charset=ISO-8859-1; format=flowed
From:
Aryeh Weiss <[log in to unmask]>
Parts/Attachments:
text/plain (32 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Michael Weber wrote:

> 
> Regarding the scan speed vs. averaging, I have the impression that
> averaging is the better way to go. With a constant light source as sample,
> reducing the scan speed results in a rather linear decrease of noise,
> whereas averaging gives exponential decrease. Based on these measurements,
> up to 8 times averaging is better than decreasing the speed to the similar
> period.
> 

This surprises me. How can averaging give an exponential decrease? I would 
expect the S/N to increase as the square root of the number of averages.

In addition, if one considers the sum of N scans, it will include the sum of N 
readouts (ie, N x readout noise). On the other hand, increasing dwell time x N 
will increase the signal by a factor of N, but will only subject the signal to a 
single readout. So I dont understand the above observation.

--aryeh
-- 
Aryeh Weiss
School of Engineering
Bar Ilan University
Ramat Gan 52900 Israel

Ph:  972-3-5317638
FAX: 972-3-7384050

ATOM RSS1 RSS2