Genomics Insights Day Peru

Date: May 26, 2026May 26, 2026
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Le invitamos a participar en el exclusivo GENOMICS INSIGHTS DAY, un encuentro que reunirá a expertos y líderes clínicos para explorar los avances más recientes en genómica aplicada, oncología y diagnóstico de enfermedades raras.
 
El evento contará con la participación de especialistas y clientes que compartirán su experiencia real en la práctica clínica, abordando temas de alto impacto: desde la implementación de paneles de cáncer hereditario hasta el uso del exoma clínico como solución multipanel para el diagnóstico genético de enfermedades raras. La jornada culminará con una visión integral presentada por nuestro equipo sobre el rastreo del cáncer: del riesgo hereditario a la detección en tempo real.
 
Asimismo, el evento destacará experiencias reales de clientes que compartirán su práctica clínica utilizando la plataforma SOPHiA DDM™, ofreciendo una perspectiva concreta sobre su impacto en el diagnóstico y la toma de decisiones.
 
A continuación, encontrará la agenda preliminar del evento

What: SOPHiA GENETICS exclusive networking event

Date: 26 de mayo

Time: 18h:00-21h:30

Where: Belmond Miraflores

Agenda

18:00 – 18:30
Bienvenida - SOPHiA GENETICS & MASED: Potenciando la Genómica en Perú

18:30 – 19:00
Optimización del diagnóstico de enfermedades raras pediátricas mediante plataforma SOPHiA GENETICS: reporte de dos casos
Dr. Nelson Purizaca
Médico asistente del Servicio de Genética y Errores Innatos del Metabolismo, Instituto Nacional de Salud del Niño, Perú

19:00 – 20:00
El Exoma Clínico: una solución multipanel.
Diagnóstico genético de enfermedades raras

Juan Martín Marques, PhD,
Líder de Servicios de NGS, Laboratorio de Biología Molecular del Sanatorio Americano , Uruguay

20:00 - 20:30
Rastreando el Cáncer: Del Riesgo Hereditario a la Detección en Tiempo Real
Bruno Piovezan, Msc.
Subject Matter Expert LATAM
SOPHiA GENETICS

20:30 – 21:30
Cocktails & Networking

Why Attend?

Discover

Discover how SOPHiA DDM™ enables accurate  analysis across multiple disease areas – from oncology to inherited disorders

Connect

Connect with your peers and Enjoy a networking environment with your peers and users of SOPHiA DDM™ Platform.

Discuss

Discuss the future of research and healthcare institutions to harness NGS data for quick, robust, and actionable insights, guiding best decisions.

Register Now

Disclaimer notice:
The term SOPHIA used by the speaker refers to SOPHiA GENETICS and its products.
The opinions expressed during this presentation are those of the speakers and may not represent the opinions of SOPHiA GENETICS.
SOPHiA GENETICS does not provide support in the validation of custom products for clinical use.
SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us at [email protected] to obtain the appropriate product information for your country of residence.

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.

SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us to obtain the appropriate product information for your country of residence.

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