SEQanswers

Go Back   SEQanswers > Introductions



Reply
 
Thread Tools
Old 01-30-2011, 02:49 AM   #1
linazel
Junior Member
 
Location: Jerusalem Israel

Join Date: Jan 2011
Posts: 2
Talking Hello everyone

Hi, my name is Lina and I'm new to the SEQanswers site/forum and to the next-gen world as well
I'm a bit lost when it comes to next-gen seq and I'm hoping that you can help me make some sense in it all and later maybe I can be of service to others as well.
I study hereditary retinal degenerations and I'm doing my first exsome sequencing and was hoping that you could recommend me some tools for analysis.
Thanks,
Lina

PS I apologies for any spelling/grammar mistakes in advance, English is not my native tongue
linazel is offline   Reply With Quote
Old 01-30-2011, 09:34 AM   #2
gprakhar
Member
 
Location: India

Join Date: Aug 2010
Posts: 78
Default

What kind of analysis do you want to perform on the data?
gprakhar is offline   Reply With Quote
Old 01-31-2011, 06:34 AM   #3
linazel
Junior Member
 
Location: Jerusalem Israel

Join Date: Jan 2011
Posts: 2
Default

I'm screening a patient to find a homozygous mutation, so I need to filter out all the SNPs and non pathogenic chages.
linazel is offline   Reply With Quote
Reply

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off




All times are GMT -8. The time now is 08:26 AM.


Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2020, vBulletin Solutions, Inc.
Single Sign On provided by vBSSO