Sunday, June 13

08:30 – 10:00 hrs | Concurrent Symposia S01-05 & Educational Sessions E05-E06

S01 | Machine learning methods for prioritizing genetic variants

Room: Hall 3

S01.1 The quest for deep knowledge – decoding the human genome with deep learning models

Olga Troyanskaya;
United States

S01.2 Leveraging public epigenomic datasets to examine the role of regulatory variation in the three-dimensional organization of the genome

Sushmita Roy;
United States

S01.3 Combining regulatory genomics deep learning with rare-variant association tests

Uwe Ohler;
Germany

S02 | Spatial omics

Room: Clyde

S02.1 Imaging the accessible genome at nanometer scale

James Zhe Liu;
United States

S02.2 Spatially resolved gene expression

Joakim Lundeberg;
Sweden

S02.3 Reading and visualizing single-cell genomes

Pierre Neveu;
Germany

S03 | Transposons

Room: Lomond Auditorium

S03.1 Journeying through the human endovirome, from species-specific biology to precision oncology

Didier Trono;
Switzerland

S03.2 Models to study the impact of active retrotransposons on the genome

Jose Garcia-Perez;
United Kingdom

S03.3 Activation of transposons in neurological disorders

Johan Jakobsson;
Sweden

S04 | Impact of GDPR on genomic data sharing

Room: Hall1

S04.1 How to transfer genomic data internationally in compliance with the GDPR

Heidi B. Bentzen;
Norway

S04.2 Is the GDPR preventing international genomic data sharing?

Jasper Bovenberg;
The Netherlands

S04.3 1+ Million Genomes Initiative and the GDPR

Regina Becker;
Luxembourg

S05 | Endogenous and exogenous mutagenesis in cancer

Room: M1

S05.1 DNA damage maps

Anna Poetsch;
Germany

S05.2 DNA damage due to suppression of DNA repair in tumorigenesis

Peter Glazer;
United States

S05.3 Mutational signatures of environmental and chemotherapeutic agents in the genomes of human cells

Jill Kucab;
United Kingdom

E05 | Pharmacogenomics in the clinic

Room: Hall 2

E05.1 Pre-emptive pharmacogenetic testing in clinical practice

Jesse J. Swen;
The Netherlands

E05.2 Pharmacogenomics: Saving lives with personalized treatment

Jatinder Lamba;
United States

E06 | Rhythm matters

Room: Hall 5

E06.1 Inherited arrhythmia syndromes

Connie R. Bezzina;
The Netherlands

E06.2 Intoduction to the arrhytmogenic disorders

Johan Saenen;
Belgium

08:30 – 10:00 hrs | Corporate Satellites

More information

10:00 – 10:30 hrs | Coffee Break, Exhibition, Poster Viewing

10:30 – 12:00 hrs | Concurrent Sessions C08-C15 from submitted abstracts

C08 |

Chairs: tba
Room: A6+A7

C08.1 Project Baby Bear: The first state-funded quality improvement project of rapid Whole Genome Sequencing in neonatal and pediatric intensive care units in the USA

Katarzyna A. Ellsworth, S. Caylor, W. Benson, C. Ashburner, J. Carmichael, E. Cham, S. Chowdhury, J. Cleary, A. D’Harlingue, L. Farnaes, J. Hunt, C. Hobbs, K. Houtchens, P. Joe, J. Knight, A. Kochhar, M. Joseph, J. Limon, M. Martin, S. Nahas, K.A. Rauen, A. Schwarz, S.P. Shankar, R. Spicer, M. Rojas, O. Vargas-Shiraishi, K. Wigby, N. Zadeh, S. Kingsmore, D. Dimmock;
San Diego, United States

C08.2 Integration of genome sequencing into health care – experiences from 3211 rare disease patients show high diagnostic rates across multiple clinical entities

Anna Lindstrand, H. Stranneheim, K. Lagerstedt-Robinson, M. Kvarnung, N. Lesko, D. Nilsson, B. Anderlid, H. Arnell, C. Backman Johansson, M. Barbaro, E. Björck, H. Bruhn, J. Eisfeldt, M. Engvall, C. Freyer, G. Grigelioniene, P. Gustavsson, A. Hammarsjö, M. Hellström-Pigg, A. Jemt, M. Laaksonen, S. Lind Enoksson, M. Magnusson, H. Malmgren, K. Naess, M. Nordenskjöld, M. Oscarson, M. Pettersson, C. Rasi, A. Rosenbaum, E. Sahlin, T. Stödberg, B. Tesi, E. Tham, H. Thonberg, U. von Döbeln, S. Vonlanthen, A. Wikström, J. Wincent, O. Winqvist, A. Wredenberg, S. Ygberg, R.H. Zetterström, P. Marits, M. Johansson-Soller, M. Johansson Soller, A. Nordgren, V. Wirta, A. Wedell;
Stockholm, Sweden

C08.3 Genomic loci susceptible to systematic sequencing bias in clinical whole genomes

Timothy M. Freeman*, Genomics England Research Consortium, D. Wang, J. Harris;
Sheffield, United Kingdom

C08.4

Systematic analysis of short tandem repeats in 38,256 exomes provides additional diagnostic yield

Bart P.G.H. van der Sanden*, M. de Groot, J. Corominas, M. Pennings, R.P.P. Meijer, L.E.L.M. Vissers, E. Kamsteeg, C. Gilissen;
Nijmegen, Netherlands

C08.5 A cost-effectiveness and utility analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients

Alison Yeung, N.B. Tan, T.Y. Tan, Z. Stark, N. Brown, M.J. Hunter, M. Delatycki, C. Stutterd, R. Savarirayan, G. McGillivray, R. Stapleton, S. Kumble, L. Downie, M. Regan, S. Lunke, B. Chong, D. Phelan, G. Brett, A. Jarmolowicz, Y. Prawer, G. Valente, Y. Samarinsky, M. Martin, C. McEwan, I. Goranitis, C. Gaff, S.M. White;
Parkville, Australia

C08.6 The impact of the 100,000 Genomes Project on rare disease in national healthcare

Damian Smedley, S. Abbs, G. Arno, E. Baple, M. Barnes, P. Beales, M. Bitner-Glindzicz, G. Black, P. Brennan, G. Chan, P. Chinnery, V. Cipriani, S. Ellard, J. Ellingford, P. Elliott, H. Firth, F. Flintner, K. Ibanez Garikano, H. Houlden, M. Irving, J. Jacobsen, E. McDonagh, D. McMullan, L. Moutsianas, W. Newman, W.H. Ouwehand, T. Ratnaike, A. Rueda Martin, C. Penkett, F. Raymond, J. Sayer, R. Scott, K. Smith, H. Stark, K. Stirrups, J. Taylor, E. Thomas, A. Tucci, J. Vandrovcova, L. Vestito, A. Webster, W. Wei, M. Wielscher, H. Williams, A. Wilkie, C. Wright, A. Rendon, M. Caulfield, ,. NIHR BioResource, ,. Genomics England Research Consortium;
London, United Kingdom

C09 |

Chairs: tba
Room: A8

C09.1 The Australian Genomic Health Alliance Mitochondrial Flagship – A national approach to genomic diagnostics

David Thorburn, N. Baker, S. Balasubramaniam, D. Bratkovic, D. Coman, A. Compton, M. Delatycki, C. Ellaway, M. Fahey, J. Fletcher, A. Frazier, R. Ghaoui, H. Goel, D. Hock, M. Kava, N. Lake, P. Lamont, J. Lee, J. Panetta, L. Phillips, R. Rius, M. Ryan, N. Smith, D. Stroud, M. Tchan, M. Walsh, M. Wallis, A. Welch, C. Wools, J. Christodoulou;
Melbourne, Australia

C09.2 High resolution respirometric analysis of a Barth Syndrome disease model

Gregor Oemer*, K. Lackner, J. Koch, E.R. Werner, C. Doerrier, G. Krumschnabel, G. Leman, S. Dubrac, R. Houtkooper, J. Zschocke, M.A. Keller;
Innsbruck, Austria

C09.3 Recurrent de novo ATAD3 duplications cause fatal perinatal mitochondrial cardiomyopathy, persistent hyperlactacidemia, encephalopathy and heart-specific mitochondrial oxidative phosphorylation complex I deficiency.

A.E. Frazier, Alison G. Compton, Y. Kishita, D.H. Hock, A.E. Welch, S.S.C. Amarasekera, R. Rius, L.E. Formosa, A. Imai-Okazaki, D. Francis, M. Wang, N.J. Lake, S. Tregoning, J.S. Jabbari, A. Lucattini, K.R. Nitta, A. Ohtake, K. Murayama, D.J. Amor, G. McGillivray, F.Y. Wong, M.S. van der Knaap, R.J. Vermeulen, E.J. Wiltshire, J.M. Fletcher, B. Lewis, G. Baynam, C. Ellaway, S. Balasubramaniam, K. Bhattacharya, M.L. Freckmann, R.J. Taft, S. Sadedin, M.J. Cowley, A.E. Minoche, S.E. Calvo, V.K. Mootha, M.T. Ryan, Y. Okazaki, D.A. Stroud, C. Simons, J. Christodoulou, D.R. Thorburn;
Melbourne, Australia

C09.4 Hyperuricemia and gout caused by missense mutation in D-lactate dehydrogenase, revealing novel enzymatic activity

Max Drabkin*, Y. Yogev, L. Zeller, R. Zarivach, R. Zalk, D. Halperin, O. Wormser, E. Gurevich, D. Landau, R. Kadir, Y. Perez, O.S. Birk;
Beer-Sheva, Israel

C09.5 Metabolite set enrichment improves biomarker identification and detection in untargeted metabolic profiling (UMP) data for patients with inborn errors of metabolism

Brechtje Hoegen*, U.F.H. Engelke, K.L.M. Coene, J.E. Hampstead, P. Kulkarni, R.A. Wevers, H.G. Brunner, C. Gilissen;
Nijmegen, Netherlands

C09.6 A genome-wide association study for a proxy non-alcoholic fatty liver phenotype identifies novel loci and trait-relevant candidate genes

M. Vujkovic, S. Ramdas, K. Gawronski, K. Lorenz, M. Serper, D.E. Kaplan, R. Carr, K.M. Lee, S. Saiju Pyarajan, T. Edwards, D. Klarin, Y.V. Sun, D.R. Miller, P.D. Reaven, L.S. Phillips, C.J. O’Donnell, J.B. Meigs, P.W.F. Wilson, R. Vickers-Smith, H.R. Kranzler, A.C. Justice, M. Gaziano, S. Muralidhar, S.L. DuVall, T.L. Assimes, J.S. Lee, P.S. Tsao, D.J. Rader, C.D. Brown, S.M. Damrauer, J.A. Lynch, D. Saleheen, Benjamin F. Voight, K.M. Chang, on behalf of the VA Million Veteran Program;
Philadelphia, United States

C10 |

Chairs: tba
Room: A3

C10.1 Recessive vs dominant GWAS of 82,516 coding variants on electronic health records in a population-wide analysis of 176,899 Finns

Henrike O. Heyne, J. Karjalainen, S.M. Lemmelä, FinnGen, A.S. Havulinna, M. Kurki, A. Palotie, M.J. Daly;
Helsinki, Finland

C10.2 Germline genetic testing following tumor sequencing in cancer patients has a remarkably high yield of clinically important findings that inform patient care

Stephen Lincoln, K. Das, N. Ngo, S. Michalski, S. Yang, D. Pineda, E. Esplin, S. Aradaya, R. Nussbaum;
San Francisco, United States

C10.3 The first genotype-phenotype study on European carriers of CDH1 germline mutations

José García-Peláez*, R. Monteiro, L. Sousa, H. Pinheiro, S. Castedo, L. Garrido, M. Teixeira, G. Michils, V. Bours, R. de Putter, L. Golmard & M. Blanluet, C. Colas, P. Benusiglio, S. Aretz & I. Spier, R. Hüneburg, L. Gieldon, E. Schröck, E. Holinski-Feder & V. Steinke, D. Calistri & G. Tedaldi, G. Ranzani, M. Genuardi, C. Silveira & I. Silva, M. Krajc & A. Blatnik, S. Novakovic, A. Patiño-García, J. Soto, C. Lázaro, G. Capellá, J. Brunet-Vidal, J. Balmaña, E. Domínguez-Garrido, M. Ligtenberg, E. Fewings, R. Fitzgerald, E. Woodward, G. Evans, H. Hanson, K. Lagerstedt-Robinson, S. Bajalica-Lagercrantz, C. Egas, C. Martínez-Bouzas et al., K. Dahan & D. Feret, N. Hoogerbrugge, M. Tischkowitz, C. Oliveira;
Porto, Portugal

C10.4 Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of 5182 cases from long QT syndrome and Brugada syndrome consortia cohorts and gnomAD population controls

Roddy Walsh, N. Lahrouchi, C. Glinge, C. Krijger, D. Skoric-Milosavljevic, N. Whiffin, F. Mazzarotto, J.S. Ware, R. Tadros, International Brugada Syndrome Genetics Consortium, International LQTS Genetics Consortium, C.R. Bezzina;
Amsterdam, Netherlands

C10.5 Genome wide association study based on cardiac magnetic resonance imaging in 23,634 individuals identifies five new loci associated with left atrial enlargement

Gustav Ahlberg*, L. Andreasen, J. Ghouse, S. Haunsoe, J.H. Svendsen, M.S. Olesen;
Copenhagen, Denmark

C10.6 Genetic interactions modulate lipid plasma levels and cellular uptake

Magdalena Zimon;, Y. Huang, A. Trasta, J. Liu, C. Chen, A. Halavatyi, P. Blattmann, B. Klaus, C. Whelan, D. Sexton, S. John, E. Tsai, W. Huber, R. Pepperkok, H. Runz;
Heidelberg, Germany

C11 |

Chairs: tba
Room: A2

C11.1 Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism

Nadja Ehmke, K. Cusmano-Ozog, R. Koenig, M. Holtgrewe, B. Nur, E. Mihci, H. Babcock, C. Gonzaga-Jauregui, J.D. Overton, J. Xiao, B. Fischer-Zirnsak, C. Huber, U. Kornak, S.H. Elsea, V. Cormier-Daire, C.R. Ferreira;
Berlin, Germany

C11.2 Integrated genome and transcriptome analyses solves about one third of the patients with rare developmental disorders and negative first-line molecular investigations

Antonio Vitobello, F. Tran Mau-Them, A.L. Bruel, Y. Duffourd, E. Tisserant, P. Callier, S. Moutton, S. Nambot, D. Lehalle, N. Jean-Marçais, J. Delanne, C. Racine, J. Thevenon, C. Poe, T. Jouan, M. Chevarin, M. Willems, C. Coubes, D. Geneviève, N. Houcinat, A. Masurel-Paulet, A. Mosca-Boidron, A. Sorlin, B. Isidor, S. Heide, A. Afenjar, D. Rodriguez, C. Mignot, D. Heron, M. Vincent, P. Charles, S. Odent, C. Dubourg, A. Faudet, B. Keren, B. Cogné, A. Boland, R. Olaso, C. Philippe, J.F. Deleuze, L. Faivre, C. Thauvin-Robinet;
Dijon, France

C11.3 Characterization and treatment of overactive K_ATP channels associated with Cantú syndrome in zebrafish

Helen I. Roessler*, S.S. Singareddy, C. McClenaghan, S. Savelberg, F. Tessadori, J. Bakkers, R. Tyron, C.G. Nichols, G. van Haaften;
Utrecht, Netherlands

C11.4 Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

Pauline E. Schneeberger*, F. Kortüm, G.C. Korenke, M. Alawi, R. Santer, M. Woidy, D. Buhas, S. Fox, D. McKnight, M. Alfadhel, B.D. Webb, E.G. Coci, R. Abou Jamra, A. Finck, M. Siekmeyer, S. Biskup, C. Heller, E.M. Maier, P. Javaher-Haghighi, M.F. Bedeschi, P.F. Ajmone, M. Iascone, H. Peeters, K. Ballon, J. Jaeken, A. Rodríguez Alonso, M. Palomares-Bralo, F. Santos-Simarro, M.E.C. Meuwissen, D. Beysen, R. Kooy, H. Houlden, D. Murphy, M. Doosti, E.G. Karimiani, M. Mojarrad, R. Maroofian, B.D. Gelb, I. Kurth, M. Hempel, K. Kutsche;
Hamburg, Germany

C11.5 C’-terminal lacking MN1 variants gain the function leading craniofacial and brain abnormalities in human

Noriko Miyake, H. Takahashi, K. Nakamura, B. Isidor, Y. Hiraki, Y. Kimura, S. Tomizawa, N. Matsumoto;
Yokohama, Japan

C11.6 A novel Bannayan-Riley-Ruvalcaba (BRRS)/CLOVES syndrome model in Xenopus tropicalis, by CRISPR/Cas9

Dionysia Dimitrakopoulou, S. Demuynck, K. Vleminckx;
Ghent, Belgium

C12 |

Chairs: tba
Room: A1

C12.1 Polygenic background of psychotic disorders and genetic determinants of disease severity

Ari V. Ahola-Olli, Z. Misiewicz, N. Mars, M. Lähteenvuo, B. Neale, T. Männynsalo, E. Isometsä, A. Wegelius, J. Hietala, W. Haaki, O. Kampman, J. Veijola, J. Tiihonen, T. Kieseppä, J. Suvisaari, S. Hyman, M. Daly, A. Palotie;
Cambridge, United States

C12.2 Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling

M. Amar, A. Pramod, V. Munive Herrera, N. Yu, L.R. Qiu, P. Moran-Losada, P. Zhang, C.A. Trujillo, J. Ellegood, J. Urresti, K. Chau, J. Diedrich, J. Chen, J. Gutierrez, J. Sebat, D. Ramanathan, J.P. Lerch, J.R. Yates III, A.R. Muotri, Lilia M. Iakoucheva;
La Jolla, United States

C12.3 Tissue-specific transcriptional and functional signatures in reciprocal genomic disorders : Insights from integrated mouse and human neuronal models

Rachita Yadav*, D. JC Tai, J. Wang, T. Aneichyk, S. Erdin, B. B Currall, K. O’Keefe, A. Stortchevoi, U. Rudolph, R. H. Perlis, J. F Gusella, M. E Talkowski;
Boston, United States

C12.4 Autism Comorbidities: Role of CHD8 during the Development of the Enteric Nervous System

Gaëlle L. Hayot*, C. Weber, C. Golzio;
Illkirch-Graffenstaden, France

C12.5 A human single-cell atlas of the Substantia nigra reveals novel cell-specific pathways associated with the genetic risk of Parkinson’s disease and neuropsychiatric disorders.

D. Agarwal, C. Sandor, V. Volpato, T. Caffrey, J. Monzon-Sandoval, R. Bowden, J. Alegre-Abarrategui, R. Wade-Martins, Caleb Webber;
Cardiff, United Kingdom

C12.6 Clinical and molecular complexity of X-linked clustering epilepsy, a disorder of cellular mosaics

Jozef Gecz, K. Kolc, L. Sadleir, C. Depienne, C. Marini, I.E. Scheffer, R.S. Moller, M. Trivisano, N. Specchio, R. Kumar, D. Pham, R. Roberts;
Adelaide, Australia

C13 |

Chairs: tba
Room: A5

C13.1 Landscape of cohesin-mediated chromatin loops in the human genome

Fabian Grubert, R. Srivas, D. Spacek, M. Kasowski, M. Ruiz-Velasco, N. Sinnott-Armstrong, P. Greenside, A. Narasimha, Q. Liu, B. Geller, A. Sanghi, M. Kulik, S. Sa, M. Rabinovitch, A. Kundaje, S. Dalton, J. Zaugg, M. Snyder;
Stanford, United States

C13.2 Analysis of chromatin looping at joint endometrial-ovarian cancer risk loci to identify candidate target genes

Dylan Glubb, I. Jeong, A. Spurdle, T. O’Mara;
Brisbane, Australia

C13.3 When the silent genome gets loud: transcription of repeated genomic elements at the single-cell resolution in K27M-mutated high-grade gliomas

Marie Coutelier*, V. Lisi, S. Hébert, D. Faury, B. Krug, N. De Jay, N. Jabado, C.L. Kleinman;
Montreal, Canada

C13.4 CDH1 regulatory noncoding elements: a hidden master for tissue-specific E-cadherin expression

Celina São José*, A.R. Monteiro, A. Qamra, R. Acuna-Hidalgo, P. Tan, S. Mundlos, C. Oliveira;
Porto, Portugal

C13.5 Local gene co-expression: molecular characterisation, tissue specificity and its genetic control

Diogo Ribeiro*, A. Ramisch, E. Dermitzakis, O. Delaneau;
Lausanne, Switzerland

C13.6 Structural variants in HDAC9 that disrupt TWIST1 transcriptional regulation but not HDAC9 protein function are associated with craniofacial and limb malformations

Ramon Y. Birnbaum, N. Hirsch;
Beer-Sheva, Israel

C14 |

Chairs: tba
Room: A4

C14.1 Implication of FOXD2 in autosomal recessive syndromic CAKUT

Korbinian M. Riedhammer, M. Nguyen, B. Alhaddad, S.J. Arnold, G.J. Kim, U. Heemann, M. Schmidts, J. Hoefele;
Munich, Germany

C14.2 Heterozygous DACT1 mutations in patients with renal anomalies and features of Townes-Brocks syndrome

A. Christians, E. Kesdiren, I. Hennies, A.D. Hofmann, M. Trowe, F. Brand, Helge Martens*, I.A. Kindem, Z. Gucev, M. Zirngibl, R. Geffers, T. Seeman, A. Kispert, H. Billing, A. Bjerre, V. Tasic, D. Haffner, J. Dingemann, R.G. Weber;
Hannover, Germany

C14.3 Loss of UNC45A causes microvillus inclusion disease-like by impairing myosin-dependent epithelial morphogenesis

R. Duclaux-Loras, F. Charbit-Henrion, C. Lebreton, O. Nicolle, M. Rabant, C. Guerrera, A. Fabre, L. Faivre, G. Michaux, H. Uligh, F. Ruemmele, N. Cerf-Bensussan, Marianna Parlato;
Paris, France

C14.4 A comprehensive exome study of the genetic architecture of asthma reveals a putative novel patient subgroup defined by filaggrin truncating variants

Sophia R. Cameron-Christie*, H. Olsson, A. Mackay, Q. Wang, M. Hühn, D. Muthas, G. Lassi, J. Lindgren, G. Povysil, D.B. Goldstein, G. Belfield, I. Dillmann, Y. Ohne, S. Cohen, S. Young, A. Platt, S. Petrovski;
Cambridge, United Kingdom

C14.5 Random plasma glucose GWAS in 479,678 individuals: genetic relationships with impaired lung function and intestinal health

Marika A. Kaakinen, L. Jiang, A. Ulrich, L. Zudina, Z. Balkhiyarova, P. Todorov, T.H. Pers, V. Lagou, I. Prokopenko, MAGIC Investigators;
Guildford, United Kingdom

C14.6 A complementary study approach unravels novel players in the pathoetiology of Hirschsprung‘s disease

T. Mederer, Stefanie Schmitteckert, J. Volz, C. Martinez, R. Röth, T. Thumberger, V. Eckstein, J. Scheuerer, C. Thöni, F. Lasitschka, L. Carstensen, P. Günther, S. Holland-Cunz, R. Hofstra, E. Brosens, D. Schriemer, I. Ceccherini, M. Rusmini, J. Tilghman, B. Luzón-Toro, A. Torroglosa, S. Borrego, C. Szeman Tang, M. Garcia-Barcelo, P. Tam, N. Paramasivam, M. Bewerunge-Hudler, C. de la Torre, N. Gretz, G. Rappold, P. Romero, B. Niesler;
Heidelberg, Germany

C15 |

Chairs: tba
Room: Live Stream Area (Exhibition Hall)

More information will follow soon.

12:00 – 13:00 hrs | Lunch Break, Exhibition, Poster Viewing

12:00 – 13:00 hrs | Corporate Satellites

More information

13:00 – 14:00 hrs | Poster Viewing with Authors – Group A

14:15- 15:45 hrs | Corporate Satellites

More information

15:45 – 16:00 hrs | Fruit Break, Exhibition, Poster Viewing

16:00 – 17:00 hrs | Poster Viewing with Authors – Group B

17:15 – 18:45 hrs | Concurrent Symposia S06-09 & Educational Sessions E07-E09

S06 | Single cell genomics in cancer

Room: Hall 2

S06.1 Transcriptional programs of brain tumors

Claudia Kleinman;
Canada

S07 | Comparative genomics across species and populations

Room: Hall 5

S07.1 Rapid evolution of genome regulation in mammals

Duncan Odom;
Germany

S07.2 Leveraging massive-scale population genomics data to unveil functional constraints

Daniel MacArthur;
Australia

S07.3 Cross-species analysis of regulatory elements and logic using deep learning

Stein Aerts;
Belgium

S08 | Biobanks in under-represented populations

Room: Hall 1

S08.1 Ancestry characterization of the Chilean population and its relevance to health

Ricardo Verdugo;
Chile

S08.2 The Mexico Biobank Project

Andrès Moreno;
Mexico

S08.3 Ethics and inclusivity when working with indigenous populations

Emma Kowal;
Australia

S09 | Gene-based therapy for inherited liver diseases

Room: M1

S09.1 AAV gene therapy for glycogen storage diseases

Dwight Koeberl;
United States

S09.2 mRNA replacement therapy for inborn errors of liver metabolism

Paolo Martini;
United States

S09.3 Lentiviral vectors for liver-directed gene therapy

Alessio Cantore;
Italy

E07 | Variant interpretation in the clinic

Room: Hall 3

E07.1 Using genomic resources to interpret the clinical significance of rare variants

Heidi Rehm;
United States

E07.2 Intepretation of the non-protein-coding regions of the genome

Nicky Whiffin;
United Kingdom

E08 | What's new in preimplantation genetic testing?

Room: Clyde

E08.1 Status of PGT and embryo selection in the era of NGS

Antonio Capalbo;
Italy

E08.2 Good practice recommendations for the PGT applications

Martine De Rycke;
Belgium

E09 | What’s AI got to do with it?

Room: Lomond Auditorium

E09.1 AI in genomics: the present and the future

Julien Gagneur;
Germany

E09.2 Policy, ethical, legal and social issues of AI use in genomics

Sobia Raza ;
United Kingdom

19:00 – 20:00 hrs | ESHG Membership Meeting

19:00 – 20:30 hrs | Corporate Satellites

More information

Saturday

Monday

Welcome to the European Human Genetics Conference Virtual Conference

August 28–31, 2021

Sunday, June 13

08:30 – 10:00 hrs | Concurrent Symposia S01-05 & Educational Sessions E05-E06

08:30 – 10:00 hrs | Corporate Satellites

10:00 – 10:30 hrs | Coffee Break, Exhibition, Poster Viewing

10:30 – 12:00 hrs | Concurrent Sessions C08-C15 from submitted abstracts

12:00 – 13:00 hrs | Lunch Break, Exhibition, Poster Viewing

12:00 – 13:00 hrs | Corporate Satellites

13:00 – 14:00 hrs | Poster Viewing with Authors – Group A

14:15 – 15:45 hrs | Workshops W05-W11

14:15- 15:45 hrs | Corporate Satellites

15:45 – 16:00 hrs | Fruit Break, Exhibition, Poster Viewing

16:00 – 17:00 hrs | Poster Viewing with Authors – Group B

17:15 – 18:45 hrs | Concurrent Symposia S06-09 & Educational Sessions E07-E09

19:00 – 20:00 hrs | ESHG Membership Meeting

19:00 – 20:30 hrs | Corporate Satellites

Welcome to the European Human Genetics Conference
Virtual Conference