Go Back   SEQanswers > General

Similar Threads
Thread Thread Starter Forum Replies Last Post
Best way to detect SNV / InDels against reference genome? camhabib Bioinformatics 2 10-22-2015 11:47 AM
Detect large deletions srr8623 Bioinformatics 2 11-28-2012 02:18 PM

Thread Tools
Old 01-22-2018, 11:02 AM   #1
Junior Member
Location: berkeley

Join Date: Jan 2018
Posts: 6
Default NSG to detect deletions and duplications genome-wide

hi there,

I need to detect deletions and duplications genome-wide in human cells. ideally I would like to use several clones (the more the better) and detect the number of deletions and duplications in each clone. is there an easy way to do that with NSG instead of classical tiling array CGH?

lorenzo.C is offline   Reply With Quote

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 04:35 AM.

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