[Genetics] Fwd: "A Traveler's Guide to Next Generation Sequencing" - SIGN UP NOW for our newest Science webinar!

[Heidi Aisala]

----- Edelleenvälitetty viesti lähettäjältä  
sciencewebinars at aaas-science.org -----
        Päiväys: 5 Jun 2013 05:33:04 -0400
      Lähettäjä: Science Webinars <sciencewebinars at aaas-science.org>
Vastausosoite: Science Webinars <reply at mail.aaas-science.org>
        Otsikko: "A Traveler?s Guide to Next Generation Sequencing" -  
SIGN UP NOW for our newest Science webinar!
  Vastaanottaja: HEIDIAIS at paju.oulu.fi

View on mobile or on web page  
[http://app.aaas-science.org/e/es.aspx?s=1906&e=50404&elq=0518f3b95d714c56b51130a7e76abc37]
Science Webinar Series
New complimentary webinar from Science:
A Traveler?s Guide to Next Generation Sequencing: Navigating the Sea  
of Genetic Variants

You are invited to hear our panel of experts on June 12, 2013, in this  
live, online educational seminar. For more information and  
complimentary registration visit: webinar.sciencemag.org

Date: Wednesday, June 12, 2013
Time: 12 p.m. Eastern, 9 a.m. Pacific, 5 p.m. UK, 6 p.m. Central Europe
Duration: 1 hour

About This Webinar

Recent advances in technology and cost effectiveness of next  
generation sequencing has led to its progressively wider  
implementation in both research and clinical settings. The amount of  
data it produces, however, can be overwhelming?typically over three  
million variants per genome. The challenges for many researchers today  
are how to make sense of this huge volume of data in the context of  
the scientific question being asked, and how to identify those  
variants that provide meaningful and relevant information. In this  
webinar we will discuss current approaches to variant analysis and how  
they can be most effectively integrated into the next generation  
sequencing pipeline.

During the webinar, viewers will:
- Learn about various methods for analyzing and comparing variants,  
including tips and pitfalls
- Gain a fuller understanding of the importance of accurate and robust  
variant analysis
- Receive advice on managing and manipulating large data sets
- Have the opportunity to put their questions to our panel of experts!

Participants:

Ruthild Weber, M.D.
Hannover Medical School
Hannover, Germany

Scott D. Kahn, Ph.D.
Illumina
San Diego, CA

Register at: webinar.sciencemag.org

Questions? E-mail: webinar at aaas.org

Produced by the Science/AAAS Custom Publishing Office and sponsored by  
BIOBASE.


- - -

Manage Your Email Preferences / Unsubscribe
(Be sure to copy and paste the entire URL to your address bar.)
http://aaas-science.org/HEIDIAISALA?elqPURLPage=18&elq=0518f3b95d714c56b51130a7e76abc37

This email was sent to: HEIDIAIS at PAJU.OULU.FI

If you need additional help, please write to memuser at aaas.org with  
customer service code ELQ

AAAS / Science | 1200 New York Avenue NW | Washington, DC 20005 | U.S.A.
+1 202-326-6417 Toll Free in the U.S.: 866-434-(AAAS) 2227 |
Privacy Policy http://www.sciencemag.org/site/help/about/privacy.xhtml

----- Välitetty viesti päättyy -----

-------------- next part --------------
View on mobile or on web page [http://app.aaas-science.org/e/es.aspx?s=1906&e=50404&elq=0518f3b95d714c56b51130a7e76abc37]
Science Webinar Series      
New complimentary webinar from Science:
A Traveler?s Guide to Next Generation Sequencing: Navigating the Sea of Genetic Variants

You are invited to hear our panel of experts on June 12, 2013, in this live, online educational seminar. For more information and complimentary registration visit: webinar.sciencemag.org

Date: Wednesday, June 12, 2013
Time: 12 p.m. Eastern, 9 a.m. Pacific, 5 p.m. UK, 6 p.m. Central Europe
Duration: 1 hour    

About This Webinar 

Recent advances in technology and cost effectiveness of next generation sequencing has led to its progressively wider implementation in both research and clinical settings. The amount of data it produces, however, can be overwhelming?typically over three million variants per genome. The challenges for many researchers today are how to make sense of this huge volume of data in the context of the scientific question being asked, and how to identify those variants that provide meaningful and relevant information. In this webinar we will discuss current approaches to variant analysis and how they can be most effectively integrated into the next generation sequencing pipeline.

During the webinar, viewers will:
- Learn about various methods for analyzing and comparing variants, including tips and pitfalls
- Gain a fuller understanding of the importance of accurate and robust variant analysis
- Receive advice on managing and manipulating large data sets 
- Have the opportunity to put their questions to our panel of experts!

Participants:

Ruthild Weber, M.D. 
Hannover Medical School 
Hannover, Germany 

Scott D. Kahn, Ph.D.
Illumina 
San Diego, CA

Register at: webinar.sciencemag.org

Questions? E-mail: webinar at aaas.org

Produced by the Science/AAAS Custom Publishing Office and sponsored by BIOBASE.


- - -

Manage Your Email Preferences / Unsubscribe
(Be sure to copy and paste the entire URL to your address bar.)
http://aaas-science.org/HEIDIAISALA?elqPURLPage=18&elq=0518f3b95d714c56b51130a7e76abc37

This email was sent to: HEIDIAIS at PAJU.OULU.FI

If you need additional help, please write to memuser at aaas.org with customer service code ELQ

AAAS / Science | 1200 New York Avenue NW | Washington, DC 20005 | U.S.A. 
+1 202-326-6417 Toll Free in the U.S.: 866-434-(AAAS) 2227 | 
Privacy Policy http://www.sciencemag.org/site/help/about/privacy.xhtml
-------------- next part --------------
An HTML attachment was scrubbed...
URL: http://lists.oulu.fi/pipermail/genetics/attachments/20130605/5f643037/attachment.html