Βιβλιογραφία
Single-cell multi-omics map of human fetal blood in Down syndrome- In silico RNA isoform screening to identify potential cancer driver exons with therapeutic applications
- Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology
- Current and new frontiers in hereditary cancer surveillance
- Data privacy in the age of personal genomics
- Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
- Specialist multidisciplinary input maximizes rare disease diagnoses from whole genome sequencing
- The person-to-person transmission landscape of the gut and oral microbiomes