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Scientific Poster
Victor Weigman, Ph.D. | May 23, 2016

Impact of duplicate removal on low frequency NGS somatic variant calling

Cancer genomic profiles created by analysis of targeted Next Generation Sequencing (NGS) panels is emerging as a powerful tool for making informed clinical decisions. Of the critical informatics challenges to address, accurate mutation calls and allele frequency estimations after accounting for PCR-mediated artifacts are debated.   Download our scientific poster Presented at AACR 2016 Annual Meeting and learn how to improve sensitivity of NGS panels.

Experts: Jeran Stratford, Gunjan Hariani, Jeff Jasper, Chad Brown, Wendell Jones, and Victor J. Weigman Jr.
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