01RMI · October 2015–January 2021
Clinical genomics
Whole-exome and targeted-panel sequencing for inherited disorders and cancer, with variant interpretation and clinician-facing reporting.
- Germline & somatic variant review
- Reference databases & literature evidence
- Thalassemia, familial deafness & oral cancer
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02NIH · April 2021–present
Pathogen genomics
Sequencing and bioinformatics for surveillance and outbreak investigations involving emerging, re-emerging and other priority pathogens.
- Clinical & environmental samples
- Illumina & Oxford Nanopore sequencing
- Comparative genomics & phylogenetics
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