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Start Your Journey to Discovery

Single Molecule, Real-Time (SMRT) Sequencing allows you to access the full spectrum of human genetic variation to uncover the hidden heritability of disease and better understand population diversity.

Increase your genetic discovery power with a comprehensive view of structural variation so you can find novel disease genes, identify causative mutations, and reveal the underpinnings of complex disease

Our 2018 Structural Variation SMRT Grant Program is Open. Apply Now!

Want to explore the human genome with a complete view of genetic variation?

Tell us how low-coverage, whole genome sequencing will advance your disease research or population genetics study for a chance to win free SMRT Sequencing including:

  • Construction up to 3 SMRTbell libraries
  • SMRT Sequencing (up to 12 SMRT Cells)
  • Bioinformatics analysis

Submit your 250-word proposal by Friday, November 30, 2018 at 5:00 p.m. PST

One winner will be selected from all qualified applications by a panel of scientists from PacBio and the University of Minnesota Genomics Center. Read the official rules.


Thanks to our co-sponsor for making this SMRT Grant Program possible!

 

The University of Minnesota Genomics Center provides the latest and most powerful sequencing platforms giving researchers a wide range of cutting-edge solutions to fit any project scale, budget, and turnaround. As a PacBio Certified Service Provider, we undergo rigorous annual certification to guarantee our clients receive the highest quality data using the most up-to-date workflows. To learn more about the genomic services we offer, contact our highly skilled scientists.


Get Inspired

Hear how other scientists are using structural variant calling to inform their research with this short video and our resource page including workflows and the latest publications:

 

Video: Structural variant discovery with long-read sequencing

Structural Variation


Submit Your Proposal

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