E01.2 Genome sequencing in newborn screening and rare disease
25:45
E01.3 Genome sequencing in infectious diseases
57:09
Leveraging isoform-level RNA sequencing to understand rare disease pathogenesis.
31:30
PL02.2 - Analysis of over 800,000 diverse sequenced humans in gnomAD v4
1:17:22
Data-driven approaches to define rare genetic diseases
45:30
E05.1 - Next generation cytogenetics by optical genome mapping
1:55:27
Worst Fails of the Year | Try Not to Laugh 💩
17:26
tagesschau 20:00 Uhr, 05.01.2025
20:27