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Genomics Data Analyst for Rare Diseases
About the JobThe candidate will be responsible for analyzing whole exome sequencing (WES) and whole genome sequencing (WGS) data using in house software to identify genetic variation that is associated with birth defects and neurological diseases, especially copy number variants (CNVs) and other forms of structural variation, and to summarize those results for collaborators at NIH for publication in scientific journals. This position is in the laboratory of Dr. Nathan Pankratz within the Division of Computational Pathology at the University of Minnesota. The lab curren


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