Go Back   SEQanswers > General

Similar Threads
Thread Thread Starter Forum Replies Last Post
new at this and need some guidance DataDiviner RNA Sequencing 2 05-03-2012 09:08 AM
qPCR Validation of Single Sample ccard28 RNA Sequencing 1 04-25-2012 11:26 AM
Exome capture validation arvi8689 Genomic Resequencing 2 01-18-2012 01:45 AM
cutadapt: guidance on rationale for --overlap=LENGTH values mgg Bioinformatics 1 01-05-2012 09:23 AM
SAM validation errors ashwatha Bioinformatics 2 08-15-2011 08:49 PM

Thread Tools
Old 07-25-2012, 12:39 PM   #1
Junior Member
Location: Madison, WI

Join Date: Jul 2012
Posts: 5
Default Validation guidance?

Hi all,
I would like to find some good guidance documents for labs choosing to validate a new library prep kit. If you were a current NGS platform user, and you wanted to switch to a new library prep kit, what experiments would you do? Are there white papers or research articles out there detailing a good set of experiments to accomplish this goal. I'd like to hear from labs who have gone through a switch to a different kit (for example, switching from TruSeq to NEBNext kits). What did you do to convince yourself that all was well?
cknox 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 03:52 AM.

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