Webinars - Blueprint Genetics

Upcoming webinars

Webinars

Genetic Testing for Retinal Dystrophy: How to Maximize Diagnoses in Your Practice

Date: May 24, 2022

Time: 9:00 AM PST / 6:00 PM CEST

Cómo analizar e interpretar los datos obtenidos mediante secuenciación del exoma completo

Date: September 14, 2021

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

C.E.U: -

Speaker: Raquel Pérez Carro

Webinars

Bringing Clinical Value Through Enhanced Panel-based Testing & mtDNA analysis

Date: August 30, 2021

Time: 12:00 CEST

Duration: 30 min

Speaker: Dr Tero-Pekka Alastalo

Webinars

Solving Diagnostic Challenges in Difficult-to-Sequence Regions

Date: August 30, 2021

From Research to Practice: A Review of Our Latest Findings in Cardiovascular Genetics

Date: August 11, 2021

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

C.E.U: -

Speaker: Julie Hathaway

Webinars

Heritable Disorders of Connective Tissue: Clinical Considerations for Genetic Testing

Date: July 27, 2021

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

C.E.U: -

Speaker: Mitzi L. Murray

Webinars

How to Solve Challenging Cases, Part IV

Date: May 25, 2021

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

C.E.U: -

Speaker: Dr Kirsty Wells

Webinars

Tackling Uncertainty Around a VUS

Date: April 29, 2021

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Navigating Genetic Diagnostics for Hereditary Hearing Loss

Date: March 30, 2021

Time: 9:00 AM PST / 18:00 CEST

En detalle: Cómo abordar las regiones genéticas complejas en el diagnóstico clínico

Date: March 16, 2021

Time: 10:00 AM PST / 18:00 CET

Duration: 1 hour

C.E.U: -

Speaker: Rocío Sánchez Alcudia

Webinars

Resolving Diagnostic Challenges in Skeletal Dysplasia – A Clinical Overview

Date: February 23, 2021

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

C.E.U: -

Speaker: Dr Melita Irving

Webinars

In Focus: Complex Genetic Regions in Clinical Diagnostics

Date: February 04, 2021

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

Speaker: Johanna Sistonen

Webinars

From Data to Insights: How WES Variants are Interpreted and Classified

Date: January 19, 2021

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

Speaker: Dr Kirsty Wells / Dr Jennifer Schleit

Webinars

Understanding Skeletal Dysplasias—Recent Advances in Genetics

Date: December 17, 2020

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

Speaker: Alicia Scocchia

Webinars

Renal Genetics: What Genetics Professionals Need to Know About This Rapidly Evolving Subspecialty

Date: December 10, 2020

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

Speaker: Dr Xiangling Wang

Webinars

Variantes de significado incierto (VUS) – interpretación, clasificación y manejo

Date: November 24, 2020

Time: 9:00 AM PST / 18:00 CET

Duration: 1 hour

Speaker: Raquel Pérez Carro

Webinars

Introducing our Clinical Report—A Step by Step Guide for Understanding Your Patient’s Test Results

Date: November 12, 2020

Time: 8:00 AM PST / 17:00 CET

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

An Introduction to Genetic Testing: What You Need to Know When Ordering a Test

Date: October 15, 2020

Time: 16:00 CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Genetic Testing for Inborn Errors of Immunity: What’s Included In Your Test?

Date: October 08, 2020

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

Speaker: Tero-Pekka Alastalo, Joe Jacher

Webinars

The Importance of Family: When to Consider Genetic Testing for Family Members

Date: September 23, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Kirsty Wells

Webinars

Detección de CNVs – ¿Por qué es importante?

Date: September 15, 2020

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

Speaker: Raquel Pérez Carro

Webinars

Detecting Copy Number Variants – Why Is It Important?

Date: August 27, 2020

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Panels, Exomes, and Genomes: Determining an Appropriate Genetic Testing Strategy

Date: June 17, 2020

Time: 9:00 AM PST / 18:00 CEST

Duration: 1 hour

Speaker: Jennifer Schleit, PhD FACMG

Webinars

Open Access Genetic Testing Program for Patients with Inherited Retinal Disease – Workshop for Eye Care Professionals

Date: June 04, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1,5 hours

Webinars

El reto de resolver casos pediátricos complejos

Date: June 03, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Rocío Sánchez Alcudia

Webinars

How to Solve Challenging Pediatric Cases, Part III

Date: May 28, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Julie Hathaway, Kirsty Wells

Webinars

Diagnostic Challenges of ABCA4-Related Retinal Disease

Date: May 11, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Kim Gall, Kelsey Zegar

Webinars

Understanding Dementia: The Common Causes and Heritability

Date: May 07, 2020

Time: 12:00 PM PST / 3:00 PM EST

Duration: 1 hour

Speaker: Kaylee Faulkner

Webinars

Genetic Testing for Early-onset Epilepsy—Introducing a Program for Paediatric Patients in Middle East & Europe

Date: April 23, 2020

Time: 8:00 AM CEST

Duration: 45 min

Speaker: Tero-Pekka Alastalo

Webinars

Next Steps with a VUS

Date: April 16, 2020

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Increasing the Clinical Utility of Panel-Based Testing with mtDNA Analysis—a Quality Overview

Date: March 25, 2020

Time: 9:30 AM PST / 17:30 PM CET

Duration: 1 hour

Speaker: Tero-Pekka Alastalo,Massimiliano Gentile

Webinars

Common Myths About Genetic Testing

Date: January 14, 2020

Time: 9:00 AM PST / 18:00 PM CET

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Inborn Errors of Immunity: The Growing Role of Genetics

Date: December 16, 2019

Time: 12:00 PM EST / 18:00 PM CET

Duration: 1 hour

Speaker: Géraldine Gosse

Webinars

Keeping Pace: The Importance of a Shared Care Approach to Inherited Cardiovascular Disease

Date: October 30, 2019

Time: 8:30 AM PST / 16:30 PM CET

Duration: 1 hour

Speaker: Dr Andrew Krahn

Webinars

Introducing an Open Access Genetic Testing Program for Patients with Inherited Retinal Degeneration

Date: October 24, 2019

Time: 9:00 AM PST / 12:00 PM EST

Duration: 1 hour

Speaker: T. Alastalo, B. Shaberman, K. Trzupek

Webinars

Genetic Testing for Individuals with Kidney Disease: Updates and Clinical Utility

Date: October 03, 2019

Time: 11:00 AM EST / 17:00 PM CEST

Duration: 1 hour

Speaker: Dr Friedhelm Hildebrandt

Webinars

How to Solve Challenging Cases, Part II

Date: August 27, 2019

Time: 8:30 AM PST / 17:30 PM CEST

Duration: 1 hour

Speaker: Johanna Sistonen

Webinars

Behind the Scenes: What it Actually Takes to Make a Genetic Test

Date: June 24, 2019

Time: 11:30 AM EST / 17:30 PM CEST

Duration: 1 hour

Speaker: Samuel Myllykangas

Webinars

Emerging Opportunities in Resolving Difficult-to-Sequence Regions: a PKD1 Case Example

Date: June 15, 2019

Time: 13:00 PM CEST

Duration: 35 min

Speaker: Johanna Sistonen

Webinars

High Resolution CNV Detection—a Powerful Diagnostic Tool

Date: June 15, 2019

Time: 12:15 PM CEST

Duration: 40 min

Speaker: Eveliina Salminen

Webinars

How to Solve Challenging Cases, Part I

Date: May 29, 2019

Time: 09:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Jennifer Schleit, Lucia Guidugli

Webinars

What If It’s a Variant of Uncertain Significance?

Date: April 30, 2019

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Improved Diagnostic Yield in Rare Hereditary Disorders -Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions

High-quality Genetic Diagnostics of Polycystic Kidney Disease with NGS Technology

Date: March 26, 2019

Time: 9:00 AM PST / 17:00 PM CET

Duration: 1 hour

Speaker: Tero-Pekka Alastalo

Webinars

Genetic Testing to Enhance the Value of a Patient Registry: A Case Study in the Inherited Retinal Dystrophies

Date: February 26, 2019

Time: 10:00 AM PST / 19:00 PM CET

Duration: 1 hour

Speaker: T. Alastalo, K. Branham, K. Trzupek

Webinars

Getting the Most From Exomes

Date: February 06, 2019

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

Speaker: Jennifer Schleit

Webinars

Shedding Light on Complex Regions in Genetics

Date: November 20, 2018

Time: 9:00 AM PST / 18:00 PM CET

Duration: 45 min

C.E.U: -

Speaker: Johanna Sistonen

Webinars

Utility of Genetic Testing and Application to Immune-Related Disorders

Date: October 25, 2018

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 50 min

C.E.U: -

Speaker: Lucia Guidugli

Webinars

Nucleus: Faster and Easier Access to Ordering Genetic Testing for your Patient

Date: September 25, 2018

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 25 min

C.E.U: -

Speaker: Thomas Vincent

Webinars

Raising the Bar: What to Expect from Cardiovascular Genetic Testing in 2018

Date: June 28, 2018

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 1 hour

C.E.U: -

Speaker: Julie Hathaway, Tero-Pekka Alastalo

Webinars

Understanding Variants of Uncertain Significance

Date: April 23, 2018

Time: 9:00 AM PST / 18:00 PM CEST

Duration: 45 min

C.E.U: -

Speaker: Jennifer Schleit

Webinars

Genetic Diagnostics and Targeted Therapies of Primary Immunodeficiency Diseases

Date: April 19, 2018

Time: 12:00 PM PST / 3:00 PM EST

Duration: 40 min

C.E.U: -

Speaker: Dr Jolan E. Walter

Webinars

Utilization of NGS in Genetic Diagnostics of Inherited Retinal Diseases with Panel Update

Date: March 14, 2018

Time: 12:00 PM PST / 3:00 PM EST

Duration: 50 min

C.E.U: -

Speaker: Tero-Pekka Alastalo

Webinars

Challenges in Selecting the Optimal Genetic Test for My Patient

Date: July 17, 2017

Time: 12:00 PM PST / 3:00 PM EST

Duration: 1 hour

C.E.U: -

Speaker: Tero-Pekka Alastalo

Webinars

Current Challenges and Future Directions in Genetic Variant Interpretation

Date: July 17, 2017

Time: 12:00 PM PST / 3:00 PM EST

Duration: 1 hour

C.E.U: -

Speaker: Jennifer Schleit

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Upcoming webinars

Genetic Testing for Retinal Dystrophy: How to Maximize Diagnoses in Your Practice

Cómo Resolver Casos Complejos de WES: Resultados Positivos Atípicos

Past webinars

Untangling Variants of Uncertain Significance

How to Solve Challenging WES Cases: Atypical Positive Results

Congenital Heart Disease: Key Considerations for Genetic Counseling

El análisis del ADN mitocondrial en paneles de NGS: más allá del núcleo

Beyond the Nucleus: Combining Panel-based NGS Testing with mtDNA Analysis

APOE in Focus: Considerations and Guidelines for Genetic Testing

Genetic Counselor Awareness Day—Ask our GCs!

Resonate Program for Eligible Individuals with Auditory Neuropathy

Unraveling Spinal Muscular Atrophy: Expanding Phenotypes and Treatment

Cómo analizar e interpretar los datos obtenidos mediante secuenciación del exoma completo

Bringing Clinical Value Through Enhanced Panel-based Testing & mtDNA analysis

Solving Diagnostic Challenges in Difficult-to-Sequence Regions

From Research to Practice: A Review of Our Latest Findings in Cardiovascular Genetics

Heritable Disorders of Connective Tissue: Clinical Considerations for Genetic Testing

How to Solve Challenging Cases, Part IV

Tackling Uncertainty Around a VUS

Navigating Genetic Diagnostics for Hereditary Hearing Loss

En detalle: Cómo abordar las regiones genéticas complejas en el diagnóstico clínico

Resolving Diagnostic Challenges in Skeletal Dysplasia – A Clinical Overview

In Focus: Complex Genetic Regions in Clinical Diagnostics

From Data to Insights: How WES Variants are Interpreted and Classified

Understanding Skeletal Dysplasias—Recent Advances in Genetics

Renal Genetics: What Genetics Professionals Need to Know About This Rapidly Evolving Subspecialty

Variantes de significado incierto (VUS) – interpretación, clasificación y manejo

Introducing our Clinical Report—A Step by Step Guide for Understanding Your Patient’s Test Results

An Introduction to Genetic Testing: What You Need to Know When Ordering a Test

Genetic Testing for Inborn Errors of Immunity: What’s Included In Your Test?

The Importance of Family: When to Consider Genetic Testing for Family Members

Detección de CNVs – ¿Por qué es importante?

Detecting Copy Number Variants – Why Is It Important?

Panels, Exomes, and Genomes: Determining an Appropriate Genetic Testing Strategy

Open Access Genetic Testing Program for Patients with Inherited Retinal Disease – Workshop for Eye Care Professionals

El reto de resolver casos pediátricos complejos

How to Solve Challenging Pediatric Cases, Part III

Diagnostic Challenges of ABCA4-Related Retinal Disease

Understanding Dementia: The Common Causes and Heritability

Genetic Testing for Early-onset Epilepsy—Introducing a Program for Paediatric Patients in Middle East & Europe

Next Steps with a VUS

Increasing the Clinical Utility of Panel-Based Testing with mtDNA Analysis—a Quality Overview

Common Myths About Genetic Testing

Inborn Errors of Immunity: The Growing Role of Genetics

Keeping Pace: The Importance of a Shared Care Approach to Inherited Cardiovascular Disease

Introducing an Open Access Genetic Testing Program for Patients with Inherited Retinal Degeneration

Genetic Testing for Individuals with Kidney Disease: Updates and Clinical Utility

How to Solve Challenging Cases, Part II

Behind the Scenes: What it Actually Takes to Make a Genetic Test

Emerging Opportunities in Resolving Difficult-to-Sequence Regions: a PKD1 Case Example

High Resolution CNV Detection—a Powerful Diagnostic Tool

How to Solve Challenging Cases, Part I

What If It’s a Variant of Uncertain Significance?

Improved Diagnostic Yield in Rare Hereditary Disorders - Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions

High-quality Genetic Diagnostics of Polycystic Kidney Disease with NGS Technology

Genetic Testing to Enhance the Value of a Patient Registry: A Case Study in the Inherited Retinal Dystrophies

Getting the Most From Exomes

Shedding Light on Complex Regions in Genetics

Utility of Genetic Testing and Application to Immune-Related Disorders

Nucleus: Faster and Easier Access to Ordering Genetic Testing for your Patient

Raising the Bar: What to Expect from Cardiovascular Genetic Testing in 2018

Improved Diagnostic Yield in Rare Hereditary Disorders -Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions