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Bridging the Gap: A Clinical Genetic Counselor's Guide to Molecular Diagnostics and Variant Interpretation


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Bridging the Gap: A Clinical Genetic Counselor's Guide to Molecular Diagnostics and Variant Interpretation Banner

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Add to Calendar Bridging the Gap: A Clinical Genetic Counselor's Guide to Molecular Diagnostics and Variant Interpretation 1/5/2024 8:00:00 AM 12/31/2024 11:59:00 PM America/New_York For More Details: https://upenn.cloud-cme.com/BridgingtheGap Description: This CourseWill Be Closed On DECEMBER 31, 2024. If you have not completed the modulesbythen,you will be required to start from the beginning once the new course is published in January 2025. This free ten-part series is designed to provide practical education on molecular diagnostics and variant interpretation to clinical genetic counselors. This series will allow genetic counselors practicing in all settings to gain c... Online false MM/DD/YYYY


Date & Location
Friday, January 5, 2024, 8:00 AM - Tuesday, December 31, 2024, 11:59 PM, Online

Course Overview


This Course Will Be Closed On DECEMBER 31, 2024.
If you have not completed the modules by then, you will be required to start from the beginning once the new course is published in January 2025.

This free ten-part series is designed to provide practical education on molecular diagnostics and variant interpretation to clinical genetic counselors. This series will allow genetic counselors practicing in all settings to gain confidence and familiarity with molecular diagnostic methodology, tools and algorithms used for somatic and constitutional variant interpretation, practical examination of clinical cases, and consideration of related topics such as genetic test utilization and equity in genetic testing. 

Please find the instructions to complete the Bridging the Gap modules, here.

The first 250 Genetic Counselors who complete all modules and evaluations will have their NSGC credit fees covered.  Once your completion of the modules is confirmed, you will receive a link to complete the online evaluations for each module.  Individuals will not be eligible for NSGC CEU credits until all modules and course evaluations are complete.

CEU submissions to the NSGC for Genetic Counselors will be take place quarterly on April 1, 2024, July 1, 2024, October 1, 2024 and at the conclusion of this program.


Target Audience
Specialties - CLINICAL BIOCHEMICAL GENETICS, CLINICAL CYTOGENETICS AND GENOMICS, CLINICAL GENETICS AND GENOMICS (MD), CLINICAL MOLECULAR GENETICS AND GENOMICS, GENETICS, MEDICAL GENETICS AND GENOMICS - Medical Biochemical Genetics, MEDICAL GENETICS AND GENOMICS - Molecular Genetic Pathology, PREVENTIVE MEDICINE - Clinical Informatics
Professions - Genetic Counselors

Learning Objectives

After completing this activity, participants should be able to:


  1. Examine molecular testing methods utilized in clinical genetic testing
  2. Explore tools and algorithms for somatic and constitutional variant interpretation
  3. Highlight complexity of genetic testing through case studies, genetic test utilization, and discussion of access to genetic testing.

Accreditation
The National Society of Genetic Counselors (NSGC) has authorized The University of Pennsylvania, funded by the Warren Alpert Foundation  to offer up to 1 CEUs or 10 Category 1 contact hours for the activity Bridging the Gap: A Clinical Genetic Counselor's Guide to Molecular Diagnostics and Variant Interpretation .The American Board of Genetic Counseling (ABGC) will accept CEUs earned at this program for the purposes of genetic counselor recertification.

Elizabeth Denenberg, MS, LCGC
Clinical Genomic Scientist
Children's Hospital of Philadelphia
Philadelphia, PA
Stacey D. Edwards, MS, CGC
Genetic Counselor
Baylor College of Medicine
Houston, TX
Elizabeth Fanning, MS, LCGC
Clinical Genomic Scientist II/Genetic Counselor
Children's Hospital of Philadelphia
Philadelphia, PA
Hannah Helber, MS, CGC
Instructor
Baylor College of Medicine and Texas Children's Hospital
Houston, TX
Alexander Y Ing, MS, LCGC
Assistant Professor
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, IL
Latrice Landry, MS, PhD
Instructor
Penn Medicine
Philadelphia, PA
Lauren Lulis, MS, LCGC
Genetic Test Utilization Program Manager
Children's Hospital of Philadelphia
Philadelphia, PA
Nichole Owen, PhD
Assistant Professor
Baylor College of Medicine
Houston, TX
Katharina Schulze, PhD
Assistant Laboratory Director
Baylor College of Medicine/Texas Children's Hospital
Houston, TX
Liesbeth Vossaert, PhD, FACMG
Associate Clinical Director
Baylor College of Medicine
Houston, TX
Lauren Westerfield, MS
Assistant Professor
Baylor College of Medicine
Houston, TX

Module 1: The Evolution of Genomic Diagnostics and its Impact on the Clinical Landscape

Please note that all 10 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

 

Register
Module 2: Methodologies for SNV and CNV detection

Please note that remaining 8 modules must be completed in order to finish the course.

 Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

 

Register
Module 3: Gene Curation

Please note that remaining 7 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

 

Register
Module 4: Variant Interpretation Tools used in Sequence, Copy Number and Somatic Variant Analysis

Please note that remaining 6 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

Register
Module 5: Constitutional SNV Interpretation

Please note that remaining 5 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

 

Register
Module 6: The genetic counselor’s introduction to tumor profiling in pediatric cancer

Please note that remaining 4 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

 

Register
Module 7: Copy Number Variant (CNV) Interpretation for constitutional variants

Please note that remaining 3 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

Register
Module 8: Clinical Applications: Panels vs. Exome Sequencing vs. Genome Sequencing

Please note that remaining 2 modules must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

Register
Module 9: Putting it all Together – Germline Clinical Case Presentations

Please note that remaining module must be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

Register
Module 10: Race, Equity, Genetic Testing

Please note that this is the last module to be completed in order to finish the course.

Each video must be watched in its entirety to continue to the post-tests. The videos cannot be paused or fast forwarded. The system will not tally each video watched to register 100%. 

Once you are taken to the Evaluation & Certificate tab, extend the date to 12/6/2025 for the Evaluation button to appear.

Register

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