Jennifer Poitras presents her poster at #ASHG2018 in San Diego on concordance of BRCA1/2 variant classification in QCI with ENIGMA expert panel assessments in ClinVar.

Capture all relevant inherited mutations, including CNVs, SNVs, InDels and Fusions, for a range of rare hereditary diseases with an end-to-end #NGS workflow combined with #HGMD. Find out how at #ASHG booth #1339

Need advice on handling precious and challenging samples? Whatever research puzzle you are trying to solve, QIAGEN #Genomic Services are here to help. Book a free consultation today

Dr. Wenbo Xu, Lab Director at True Health Diagnostics, on the challenges faced in next generation sequencing when dealing with SNV's and CNV's, and the opportunity the new QIAseq panel brings to this field of research. #ASHG2018