Fecha límite de inscripción para ser considerado al curso:
20/11/2023
Fecha límite de inscripción para ser considerado al curso:
20/11/2023
Curso práctico de genómica.
27 AND 28TH APRIL 2026 (FULL DAY): PLEASE NOTE THAT COURSE 1 (16S/Metagenomics) and COURSE 2 (Exome sequencing and analysis) are PRE-MEETING COURSES WHICH WILL TAKE PLACE IN 27 AND 28 TH APRIL 2026 (https://www.nupemgenomicweek.com/hands-on-course)
Se seleccionarán hasta 10 investigadores para participar en nuestro curso práctico, donde aprenderán las diferencias entre Illumina y las plataformas de nanoporos, y cómo preparar una biblioteca de ADN de alta calidad para su secuenciación.
La selección se realizará en función del análisis de CV y la carta de recomendación de IP. Se dará prioridad a estudiantes de posgrado de diferentes laboratorios.
COURSE 2 – EXOME SEQUENCING AND RARE DISEASE DIAGNOSIS
CONTENT: EXOME SEQUENCING IN PERSONALIZED MEDICINE
COORDINATION: Dra. Natana Rabelo (Supervisora de Análises Genômicas no Laboratório de Biologia Molecular / Medicina Genômica - IFF/Fiocruz); Dra. Maria Eduarda Gomes (Supervisora de P&D em Genômica e Analista Genômica no Laboratório de Biologia Molecular / Medicina Genômica - IFF/Fiocruz) e Eder Soares Pires (Illumina)
This course focuses on the principles and applications of Whole Exome Sequencing (WES) in clinical and biomedical research. Participants will be guided through the full analytical pipeline, including read alignment, variant calling, annotation, filtering, and interpretation of coding variants. Special attention is given to variant pathogenicity assessment and the integration of genomic data with clinical information. The course is designed for researchers and healthcare professionals seeking a solid methodological foundation to translate exome data into biologically and clinically meaningful insights.