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Sessions included in the “EMPAG” Track
08:30 – 10:00 |
Concurrent Symposia S01 – S04  S01 Updates in psychiatric genetics  S02 Finding the strengths that make cancer cells weak S03 RNA mis-splicing dynamics, diagnosis and treatment S04 An update on kidney research |
Educational Sessions E05-E06  E05 The longer the better? Third generation sequencing technologies E06 Pharmacogenomic testing for personalized medicine |
10:00 – 10:15 |
Coffee Break, Free Poster Viewing, Exhibition |
10:15 – 11:15 |
Poster Viewing with Authors and coffee (Group A) |
11:15 – 12:45 |
Corporate Satellites  |
11:15 – 13:00 |
Free Poster Viewing – Exhibition – Lunch |
13:00 – 14:30 |
Concurrent Sessions C08 – C15  C08 Prenatal Genetics C09 Cancer genetics C10 Cardiovascular disorders C11 Statistical and population genetics C12 Intellectual Disability C13 Pharmacogenomics C14 Genetic counselling developments  C15 Best Posters 1 |
14:30 – 15:00 |
Fruit Break – Free Poster Viewing – Exhibition |
15:00 – 16:30 |
Workshops W05 – W11  W05 Exome sequencing and variant interpretation W06 Dysmorphology I W07 UCSC Genome Browser W08 Investigating genotype-phenotype data using the GWAS Catalog W09 A Tribute to Seymour Kessler: Deliberating Psychotherapeutic Work in Genetic Counseling  W10 Genomics Quiz W11 European funding schemes for researchers |
15:00 – 16:30 |
Corporate Satellites  |
16:30 – 16:45 |
Coffee Break, Free Poster Viewing, Exhibition |
16:45 – 17:45 |
Poster Viewing with Authors and coffee (Group B) |
17:45 – 19:15 |
Concurrent Symposia S05 – S08  S05 Genome editing S06 Thank you for the Variant (a personal utility tale)  S07 Polylygenic risk scores coming of age S08 Beware of the transposons |
Educational Sessions E07-E08  E07 Single-cell transcriptomics in the brain E08 Chromosome Y loss and the ageing genome
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19:15 – 20:15 |
ESHG Membership Meeting |
19:15 – 20:45 |
Corporate Satellites  |
08:30 – 10:00 |
Concurrent Symposia S09 – S12  S09 Multidimensional nuclear organization S10 From genome wide association study to mechanisms: fine-mapping S11 „De novo““ developments in epilepsia S12 Congenital disorders of glycosylation |
Educational Sessions E09-E10  E09 Variant interpretation and high-throughput functional assays E10 Meiosis: factory of genetic variation |
ELPAG Award Lecture A1  |
10:00 – 10:15 |
Coffee Break, Free Poster Viewing, Exhibition |
10:15 – 11:15 |
Poster Viewing with Authors and coffee (Group C) |
11:15 – 12:45 |
Corporate Satellites  |
11:15 – 13:00 |
Free Poster Viewing – Exhibition – Lunch |
13:00 – 14:30 |
Concurrent Sessions C16 – C23  C16 Personalized and predictive medicine C17 Genetic mechanisms in cancer C18 Therapies C19 From genome architecture to RNA biology C20 Neuromuscular and neurodegenerative disorders C21 Internal organs C22 Ethical, policy and psychosocial aspects in genomics  C23 Best Posters 2 |
14:30 – 15:00 |
Fruit Break – Free Poster Viewing – Exhibition |
15:00 – 16:30 |
Workshops W12 – W18  W12 Dysmorphology II W13 Copy Number Variant Interpretation and Classification W14 Molecular Newborn screening vs. newborn testing W15 European Reference Networks – What is in it for me? W16 Opportunistic or non opportunistic genetic screening?  W17 Using Ensembl data and tools: a worked clinical example W18 Pharmacogenomics in practice |
15:00 – 16:30 |
Corporate Satellites  |
16:30 – 16:45 |
Coffee Break, Free Poster Viewing, Exhibition |
16:45 – 17:45 |
Poster Viewing with Authors and coffee (Group D) |
17:45 – 19:15 |
Concurrent Symposia S13 – S16  S13 Understanding mutations to detect cancer S14 Debate: Genomics and the Media  S15 Regulatory Landscapes S16 Methods for genetic epidemiology |
Educational Sessions E11-E12  E11 Genome First Testing in Pediatrics (joint Session) E12 Oligogenic inheritance |
20:00 |
ESHG Networking Evening |
09:00 – 10:30 |
Concurrent Symposia S17 – S19  S17 ESHG-ASHG building bridges: Global collaboration to advance the use of genomics in health S18 Our genetic history and its phenotypic consequences S19 Treating rare genetic disease S20 Epigenetics and early development |
Educational Sessions E13-E14  E13 Genetic innovations in reproductive medicine E14 Understanding human disease through animal models |
11:00 – 12:30 |
Concurrent Sessions C24 – C29  C24 Mosaicisms C25 Bioinformatics and multiomics C26 Mitochondrial disorder C27 Developmental disorders 2 C28 Breaking Abstracts C29 Stakeholder perspectives in cancer genetics  |
12:30 – 13:30 |
Lunch Break |
13:30 – 14:15 |
PL3 Mendel Lecture  |
14:15 – 15:00 |
PL4 ESHG Award Lecture  |
15:00 – 15:45 |
PL5 Awards Session  ESHG Education Award EJHG Citation Awards ESHG Awards for Best Presentations by Young Investigators Closing |