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.

Jeran Stratfor
Gunjan Hariani
Jeff Jasper
Chad Brown
Wendell Jones, Ph.D., Principal Bioinformaticist and Scientific Advisor
Victor J. Weigman, Ph.D., Director, Translational Genomics

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