Single cell Whole genome sequencing in peripheral

The National Institutes of Health (NIH) is seeking a contractor to perform single cell whole genome sequencing in peripheral blood of patients with VEXAS syndrome. The goal of this project is to gain a better understanding of the genetic mechanisms underlying this rare disease. The contractor will be responsible for collecting and processing blood samples, performing whole genome sequencing, and analyzing the resulting data. • The contractor must have experience with single cell whole genome sequencing and analysis. • The contractor must have access to a high-throughput sequencing platform. • The contractor must be able to collect and process blood samples from patients with VEXAS syndrome. • The contractor must be able to analyze the resulting data and provide a comprehensive report of their findings.