Sunday, May 22, 2016
08.30 - 10.00 | Concurrent Symposia S01 - S04 |
S01. The future lies in uncertainty - joint with EMPAG (Plenary Hall)S01.1 Tolerating uncertainty in the clinic; The impact of new genetic technologies S01.2 Personal genomic testing: How individuals understand and respond to genetic risk information S01.3 The blessings of uncertainty in the genomics era S02. Understanding functional effects of genomic variants (Room 112)S02.1 Using single-cell RNAseq to understand effects of rare variants S02.2 RNA splicing is a primary link between genetic variation and disease S02.3 Mapping genetic effects in single-cell transcriptomes S03. Hereditary cancer (Room 117)S03.1 Hereditary colorectal cancer: Recent advances and future perspectives S03.2 Familial pancreatic cancer: advances in genetics and prevention S03.3 The genetics of skin and uveal melanoma S04. From families to populations and back (Room 113+114)S04.1 Combining family and population sequencing to elucidate the genetic architecture of cardiometabolic risk traits S04.2 Population biobanks: a crucial hub in clinical research S04.3 Cost effective designs with population specific imputation panels in the Sardinian isolate |
08.30 - 10.00 | Educational Session 5 |
E5. Ciliopathies (Room 115+116)E05.1 Cilia in human developmental anomalies E05.2 Expanding Ciliopathies | |
| 10.00 - 10.15 | Coffee Break, Exhibition |
10.15 - 11.15 | Poster Viewing with Authors - Group A |
| 11.15 - 13.00 | Free Poster Viewing, Exhibition, Lunch break |
11.15 - 12.45 | Corporate Satellites |
13.00 - 14.30 | Concurrent Sessions C07 - C12 - Click on the titles for details |
C07. Genome Technology in the Clinic (Plenary Hall) | |
| 14.30 - 15.00 | Fruit Break, Free Poster Viewing, Exhibition |
15.00 - 16.30 | Workshops WS05 - WS11 - Click on the titles to see detailed programmes |
W05. NGS in the Clinic* (Plenary Hall) |
15.00 - 16.30 | Corporate Satellites |
| 16.30 - 16.45 | Coffee Break, Free Poster Viewing, Exhibition |
16.45 - 17.45 | Poster Viewing with Authors - Group B |
17.45 - 19.15 | Concurrent Symposia S05 - S08 |
S05. Circulating Cell-Free Nucleic Acids (Plenary Hall)S05.1 NIPT versus Traditional Multiple Marker Screening for All Pregnancies—Time for Consideration S05.2 Circulating Tumour DNA & Circulating Tumour Cells: Complimentary Approaches S05.3 Genomewide plasma DNA sequencing for cancer detection and noninvasive prenatal testing S06. Behavioural disorders (Room 112)S06.1 Using next-generation sequencing to understand the genetics of autism S06.2 A highly conserved programme of neuronal microexons is misregulated in autistic brains S06.3 Genetics of schizophrenia S07. Long distance regulation of transcription and translation (Room 117)S07.1 Gene regulation dynamics and chromatin architecture during development and evolution S07.2 Dissecting mammalian transcriptional organization by analyzing the content of transcription factories S07.3 Decoding the non-coding landscape S08. Sensory disorders (Room 113+114)S08.1 Functional studies reveal how mutations of MYO15A cause human deafness DFNB3 S08.2 Genetics of visual impairment S08.3 Genetics of Pain sensitivity |
17.45 - 19.15 | Educational Session 6 |
E6. Cost-effectiveness in genetic testing (Room 115+116)E06.1 Cost-effectivness of diagnostics in rare diseases E06.2 Cost-effectivness of testing in cancer | |
19.15 - 20.45 | Corporate Satellites |
19.15 - 20.15 | ESHG Membership Meeting (Room 118+119) |