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flow cytometry data analysis Purdue University and ISAC Congress DataStandards Committee
Posted by Mitch Haynes


Workshops Tutorials Polish Cytometry Society ISAC Congress Analysis of
flow cytometric data - data collection, principles of forming an
orginization that will control the market of Flow Cytometry Software
and License Fees.

Purdue Cytometry plan 4 Isac Congress & FDA FORCE

An Idea how to Create a code and make it into a Standard that would
benifit Corporations that Develop Software

How to Create Millions of Hits on your website and only ALLOW 3000
Members through ISAC Congress.

How to Create Corporations and keep Vendors out of the the LUCRATIVE
CLINICAL market.


Purdue Cytometry Mail List Plans to have Isac Congress Persuade the
FDA to FORCE their FCS STANDARDS!

From: Randy T. Fischer (fisch...@vax.grc.nia.nih.gov) Date: Thu Jul 17
1997 - 03:25:15 EST * Next message: kc...@samsung.co.kr: "LDL Receptor
Assay for FH" * Previous message: Bob Ashcroft: "RE: Cell Culture
after DNA Ploidy Staining" * Messages sorted by: [ date ] [ thread ]
[ subject ] [ author ] [ attachment ]
________________________________________

I agree with both Marty and Gunter in the very important issue of
standardizing data formatting.

I would point out that lobbying ISAC is only, however, part of the
answer. Regardless of what ISAC may choose to recommend, it is still
up to the manufacturers to implement what they want to do,

and if they do not agree with ISAC, then too bad for ISAC

and the flow community.


A potentially more powerful force for change might be the

FDA, which regulates machines used in CLINICAL settings.

If the FDA could be persuaded

to require all CLINICAL data be universally both accessible and
readable, then the manufacurers would be forced to upgrade machines
and software

or

lose theLUCRATIVE CLINICAL market.

This would make anlyzing data from different sources easier,

and could facilitate the exchange of crucial clinical results from
various trials where multiple sites and machines are in use.

So how does this get done?

Gunter (and Paul's agreeing response) are correct this needs to be
revisited at Asilomar, with perhaps an additional idea.


Any concrete standardization protocol, FCS3.0 or whatever it ends up
being designated, should be then presented to any and all regulatory
agencies by ISAC to ensure no individual manufacturer decides FCS3.0
in their format is acceptable, even if it is not universally
readable.

Randy T. Fischer NIA/NIH GRC Baltimore, MD 21224
fisch...@vax.grc.nia.nih.gov

Now your Leaders of ISAC Congress and the Data Standards Committee

A must read

Collusion?

http://www.facebook.com/note.php?not...9772873&ref=mf






Posted by Mitch Haynes


On Aug 25, 5:52*pm, Mitch Haynes <mitchhay...@gmail.com> wrote:
http://advenet.com/flowcytometry/blo...mmentmessa ge

Posted by Mitch Haynes


On Aug 25, 5:52*pm, Mitch Haynes <mitchhay...@gmail.com> wrote:
http://advenet.com/flowcytometry/blo...mmentmessa ge