Webinar of the Month
Configuring SNP detection pipelines for accurate analysis of clinical samples
By Dr. Vamsi Veeramachaneni
Vice President, 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 15th Annual Advances in Genome Biology and Technology (AGBT) 2014 meeting to be held in Marco Island, Florida from Feb 12-15. Dr Rohit Gupta, Strand will demonstrate software for 'Detecting copy number variations in cancer using next generation sequencing data'
- Visit 'Strand Life Sciences' booth 'A6' at Bangalore India Bio 2014, Feb 10-12, Lalit Ashok, Bangalore and learn more about Clinical Genomics, Avadis NGS, research solutions and other customized services offered by Strand
- Dr Kas Subramanian, CSO, Strand will speak on 'Genomics in Clinical Practice' at the Pharmacogenomics, BioMedical Informatics and Personalised Medicine session at Bangalore India Bio 2014 on 12 Feb, 12.30 PM
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Dr Rohit Gupta, Strand will present a seminar on 'Exome Sequencing Analysis in Avadis NGS', at the workshop on 'Next Generation Sequencing Analysis on Human exome and transcriptome sequencing', R.V College of Engineering, Bangalore on 19 Feb 2014, 2.00 PM
- The Avadis NGS Team
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| Session 1:
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| Europe +Asia
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| Feb 26, 2014 |
| 10 AM Central European Time |
| Session 2:
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| North + South America |
| Feb 26, 2014 |
| 9 AM Pacific Standard Time |
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