Adam Ameur is associate professor in genomics and bioinformatics. His work is focused on development of technology and infrastructure, with the aim to improve our knowledge about the human genome and to improve the diagnostics of disease. During the last decade, AA has become a leading expert in long-read sequencing technology and its applications in medical genetics. He is also leading the effort to construct a whole genome data resource of genetic variation for the Swedish population.
Adam Ameur
Uppsala University
Key Publications
Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare
Nature Medicine, 2025
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
Genome Research, 2024
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Genome Research, 2024
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
Life Science Alliance, 2024
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
Communications Biology, 2024