Dr Ira Deveson is a mid-career researcher and Snow Fellow. He has expertise in clinical genomics, biotechnology development and bioinformatics, with his lab focusing on applications of long-read sequencing in clinical genomics. His work spans from computational methods development and software/hardware engineering, to large-scale genomic analysis of diverse cohorts in health and disease.
Dr Ira Deveson graduated with a Bachelor of Philosophy from the Australian National University in 2012. He completed a PhD at the Garvan Institute of Medical Research from 2014-2017, supervised by Prof John Mattick and Dr Tim Mercer. Dr Deveson's PhD focused on genome/transcriptome research and bioinformatics, and earned him recognition with the JD Catcheside prize from the Genomics Society of Australasia.
Dr Deveson was appointed as Head of Garvan's Genomic Technologies Lab in 2020 and has since been awarded multiple significant NHMRC and MRFF grants to support his work on long-read sequencing technology development. He currently holds an NHMRC Investigator Grant (L1) and a prestigious Snow Medical Fellowship. His research has been published in leading science journals including Nature, Nature Biotechnology and Nature Methods. In addition to his research role, Dr Deveson leads the Long-read Sequencing Hub within Garvan’s Genomics Platform.
Medical Minds Podcast
Awards
- 2026
Snow Fellowship
- 2025
Australian Academy of Science Ruth Stephens Gani Medal
- 2024
NSW Early Career Researcher of the Year (Biological Sciences)
- 2017
DG Catcheside Prize - Genetics Society of Australasia: most outstanding Australasian PhD graduate in the field of genetics
- 2012
University Medal for Biology - Australian National University: outstanding graduate from the biological sciences
Selected publications
See all publications- PUBLISHED 4 July 2026Nature Communications
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies
- PUBLISHED 24 November 2025Nature Communications
Targeted sequencing and iterative assembly of near-complete genomes
- PUBLISHED 13 December 2023Nature
The landscape of genomic structural variation in Indigenous Australians
- PUBLISHED 4 March 2022Science Advances
Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing
- PUBLISHED 3 January 2022Nature Biotechnology
Fast nanopore sequencing data analysis with SLOW5


