Collaborate with MGI


MGI provides a wide variety of sequencing and sample preparation services on multiple platforms.


Collaborative large-scale genome sequencing effort identifying rare risk & protective variants that contribute to common disease phenotypes


Supported clinical interpretations of mutations related to cancer and collaborate with colleagues to add variants and support for cancer-related mutations


NHLBI project to understand the genetics underlying heart, lung, blood and sleep disorders, including COPD

Collaboration is Key at MGI

We have spent more than a decade working with partners around the globe to help advance the field of genomics as it applies to human health and disease. Our relationships have yielded vast improvements in sequencing technology as well as the production and analysis of meaningful, clinically relevant results. Our co-investigators are able to leverage our strengths as a world-class research institute and see us as a valuable asset that enhances their scientific capabilities and impact.

  • Operating a vast array of high-throughput sequencing instruments, we apply the most technologically advanced sequencing methods available.
  • Using a powerful, well-proven analysis pipeline that detects key single nucleotide variants, insertions, deletions and structural variations, we are able to generate actionable disease targets.
  • Producing over 100 publications in world-class journals during the last five years alone, we provide manuscript and grant writing assistance and access to renowned clinical expertise.
  • With over $1.2B in funding since our inception, we have a proven track record applying exceptional project management experience to a project from start to publication.

Services Available to Collaborators

  • Clinical Sequencing - College of American Pathologists (CAP) Accredited Laboratory
  • Whole Genome Sequencing
  • Whole Exome Sequencing
  • Whole Genome Bisulfite Sequencing
  • RNA Sequencing
  • ChiP Sequencing
  • Genotyping Arrays
  • Gene Expression Assays
  • RNA Capture
  • Custom Targeted Capture
  • Single Cell Sequencing
  • Library Construction from Low-Input Specimens
  • Whole Genome Optical Mapping
  • Bioinformatics Analysis
  • Data Transfer

For more information, please contact