Webinars | Blueprint Genetics

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

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

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

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Upcoming webinars

Unraveling Spinal Muscular Atrophy: Expanding Phenotypes and Treatment

Past webinars

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

Understanding Variants of Uncertain Significance

Genetic Diagnostics and Targeted Therapies of Primary Immunodeficiency Diseases

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

Current Challenges and Future Directions in Genetic Variant Interpretation

Challenges in Selecting the Optimal Genetic Test for My Patient

Subscribe to our newsletter

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