Webinar of the Month
Configuring SNP detection pipelines for accurate analysis of clinical samples
By Dr. Vamsi Veeramachaneni
Vice President - Bioinformatics, Strand Life Sciences
Running
a SNP detection pipeline and identifying high quality variant calls
quickly is challenging. This is especially true in the case of clinical
labs where multiple panels are used and kit-specific biases can result
in false positive SNP predictions. In this webinar, we show how one can
use the powerful visualization features of Avadis NGS to quickly detect
false positive SNP predictions, identify the cause of the errors, and
fine-tune the detection pipeline for accurate analysis
Updates
- Catch us at the 2014 ACMG Annual Clinical Genetics Meeting to be held in Nashville, Tenessee from 26- 29 March 2014
- Read the latest blog on 'Mapping RefSeq transcripts to the genome using UCSC' by Dr Vamsi Veeramachaneni
- The Avadis NGS Team
No comments:
Post a Comment