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Visit Illumina at the XXIX SIGU National Congress to explore how whole-exome sequencing and whole-genome sequencing are advancing research into rare, undiagnosed and inherited genetic diseases.

Meet our experts at booth 41 to discuss streamlined, scalable and flexible sequencing and informatics strategies for genetic disease testing.

Attend the Illumina workshop

Più valore da ogni genoma: innovazioni per una genomica avanzata 

8 October | 13:00–14:00 
Room WS1, Sala della Piazza

Moderator: Dr. Daniela Piazzolla, Senior Manager, Medical Affairs, Illumina

TruPath Genoma: più semplicità e una visione più completa del genoma 
Andrea Finocchio, Staff Scientist, Illumina R&D

Il nostro percorso nella genomica: dall’esperienza di oggi alle innovazioni per risolvere i casi complessi 
Prof. Antonio Novelli, Director, Medical Genetics Laboratory, IRCCS Bambino Gesù Children’s Hospital, Rome

Genomics in Action: Where We Are 
Dr. Laura Pezzoli, NGS Lead, Medical Genetics Laboratory, ASST Papa Giovanni XXIII, Bergamo

Date & Time
7 Oct 2026 – 9 Oct 2026
Location
Rimini
Italy
Europe
Topic
Complex disease genomics, Genetic & rare diseases, Oncology
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