Overview
The gLHS Network has compiled a public repository of tools and resources which may be of interest to other institutions interested in conducting genomics-enabled Learning Health System projects. The public repository contains a wide array of resources, ranging from patient-facing and provider-facing education materials to algorithms used to identify patient cohorts based on clinical guideline criteria.
Bulleted description of lakehouse and knowledgebase
Protocol describing method for NICU surveilance
Protocol describing GARDE population based genetic testing
Protocol describing PGx Intervention
References and links for GARDE Familial Hypercholesterolemia
Additional description of GARDE Genetic Cancer Risk Detector
References and links for CDS Hooks
Additional description of HL7 CDS Hooks
Published paper described MPSE Mendelian Phenotype Search Engine
Related Published Literature
The following planning guide and economic tool were designed to help organizations decide how to implement routine tumor screening for Lynch syndrome in order to maximize success. The planning Guide may also help organizations decide whether to go straight to germline testing.
Familial Hypercholesterolemia Clinical Management Guidelines
What is Familial Hypercholesterolemia?- Educational Materials
About Familial Hypercholesterolemia- Educational Materials
Academic Detailing Services – Educational Materials
Sample Post-counseling CPRS Note
FH Letter Template containing information for patient of genetic variant
Overview of PGx, Explanation, coordination, suggested language
Screenshots of sample alerts for DPYD
Sample letter describing test result
Screenshots of sample alerts for DPYD
Pharmacogenomics Note Template
Overview & FAQ about pharmacogenomic testing, resources
Academic Detailing Services – Educational Materials