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Policiies for the genome editing core, providing investigators access to state-of-the-art genome editing technologies.


All data, results and models generated by the Genome Editing Center will be accessible only to the investigator(s) involved in the project. Data will not be shared in any way without permission from the investigator(s).

All users are charged a fee for services provided by the Genome Editing Center. All users of the center are expected to pay for the services provided. An IU account number or a purchase order number (PO#) must be provided at the start of the service. For all services, full payment is expected, regardless of the outcome. The center also reserves the right to decline taking on projects with low chance of success.

Model generation services have priority over traditional transgenic core services. All services are on a first-come first-served basis. Some projects may take longer to complete than others. The Genome Editing Center reserves the right to modify schedule to minimize the number of mice used.

The Genome Editing Center should be acknowledged in all publications or grants describing the models generated by the Center, and a copy of the publication should be provided to the Center. The following statement should be added to any publications that used the center’s services: “This work was supported by the Indiana University Genome Editing Center at Indiana University School of Medicine.”

Authorship will be granted to individual(s) involved in the design and oversight of genome editing projects. Fees paid for services provided by the Genome Editing Center do not preclude or replace authorship.

The Director of the Genome Editing Center will discuss all issues with investigators and will seek to resolve them. In the event issues arise that cannot be resolved by the center director, the center’s Advisory Committee will resolve the issues.

Material or health-related information submitted to Genome Editing Center must be obtained in compliance with current regulatory and legal requirements, that users comply with all safety standards (IRB, IBC, IACUC, others) and fully disclose the potential hazards of materials submitted.