Educational Opportunities

ACGME-Accredited ABMGG

Clinical Laboratory Genetics Training Programs


  • Laboratory Genetics and Genomics (LGG) Fellowship

The LGG training program is a two year training offered through the Wisconsin State Laboratory of Hygiene (WSLH), in partnership with PreventionGenetics, Inc., and in collaboration with UW Health, the Waisman Center, and the Department of Pediatrics. This unique relationship with our partner labs provides fellows with a diverse and well-rounded experience in all aspects of clinical cytogenetic and molecular genetic and genomic testing. This program includes formal didactic work, clinical experience, research, teaching opportunities, as well as extensive laboratory training with progressive responsibility throughout the tenure of the fellowship. Fellows will leave the program prepared to direct and interpret clinical genetic analyses relevant to the diagnosis and management of human genetic diseases at the highest level of quality.


WSLH Laboratory Genetics and Genomics Fellowship Virtual Tour


LGG Fellowship Training ScheduleLGG Fellowship Schedule diagram



  • Clinical Biochemical Genetics (CBG) Fellowship

The CBG training program is offered in partnership between the Wisconsin State Laboratory of Hygiene (WSLH) and the Department of Pediatrics, Division of Medical Genetics. This training program is designed to teach skills necessary to direct operations of an accredited biochemical genetics laboratory as well as conduct academic research as related to clinical laboratory testing. This program is offered in collaboration with the Wisconsin Newborn Screening Laboratory. This unique relationship is intended to provide a comprehensive learning environment, exposing training fellows to the field of biochemical genetics and its interface with newborn screening. Additional information regarding testing in the biochemical genetics and newborn screening laboratories can be found here.


Karyotyper icon


Karyotyper is an interactive software tool designed to train users to identify chromosomes and to begin learning the skills of cytogenetic analysis. A series of chromosome matching modules are included featuring half karyotypes, full karyotypes, and intact metaphase spreads. Initially, the user is alerted to incorrectly placed chromosomes, but the feedback becomes less immediate in more advanced modules. Karyotyper was created by an experienced cytotechnologist and can be utilized by learners at every level – from grade school students to new professionals.  Click the icon above or link here. Give it a try!


Collaborative Genomics Core

Case Conference and Molecular Tumor Board

A recurring scheduled series for CME credit via the UW Office of Continuing Professional Development (OCPD)


Global Objective- Upon completion of the activity, participants will have the ability to recognize both common and rare genetic abnormalities associated with developmental delay, infertility, prenatal ultrasound findings and oncology specimens. This activity also provides a consult opportunity for review by a molecular tumor board overseen by the UW Comprehensive Cancer Center.


 (Institutional use only)


Genetics in Wisconsin


Genetics in Wisconsin – An Online Resource for Nongenetic Providers

The Genetics in Wisconsin website was created to increase access to genetic services by providing an online resource for non-genetic healthcare providers who may consider referring to genetics or incorporating genomic medicine into their practice.

Genetics in Wisconsin provides information regarding indications for referral to genetics, elements of a genetics evaluation including commonly recommended genetic tests, informed consent videos, practice guidelines for genetic conditions, Ask an Expert feature (not a consultation service) and more.

Increased awareness of genetic services and increased availability of genetic testing, in combination with a chronic shortage of genetic providers contribute to the current access barriers patients face in receiving genetic services. Consequently, primary and specialty practitioners are increasingly challenged with bridging the access gap by integrating genomic medicine into their practice. However, non-genetic providers report variable knowledge and confidence in their ability to provide genetic services and limited access to training and resources.

The website is developed and managed by the Genetic Systems Integration (GSI) Initiative, a Maternal & Child Health (MCH) Title V Block grant funded initiative.  The GSI Initiative is housed at the University of Wisconsin – Madison Waisman Center.


For questions, please contact:

Sara Zoran, MS, CGC

Genetic Counselor, Coordinator – Genetic Systems Integration Initiatve, Waisman Center     608.262.0182

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