Author

Remi-Andre Olsen

Stockholm University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Afshin AhmadianiD· 1 shared David Redin· 1 shared Dennis KloseiD· 1 shared Erik BorgströmiD· 1 shared Ha T.H. VuiD· 1 shared Hooman AghelpasandiD· 1 shared Jason ErnstiD· 1 shared Jennifer Theland· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Afshin AhmadianORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Whole-genome profiling of native 5-hydroxymethylation in human neurons with long-read sequencing

Dennis Klose, Mohammad Hossein Sepehri, Remi-Andre Olsen, Ha T.H. Vu, Jason Ernst, Lara Kular, Maria Needhamsen, M Jagodic

The paper uses long-read sequencing to profile native 5hmC and 5mC in human neurons, showing 5hmC enrichment in transcribed regions and enhancers.

bioRxiv · Jan 12, 2026 · PreprintNeuroscience

Efficient whole genome haplotyping and high-throughput single molecule phasing with barcode-linked reads

David Redin, Tobias Frick, Hooman Aghelpasand, Jennifer Theland, Max Käller, Erik Borgström, Remi-Andre Olsen, Afshin Ahmadian

This paper introduces a barcode-linked reads technology for efficient whole genome haplotyping and long-range single molecule phasing with minimal cost increase.

Scientific Reports · Dec 2, 2019Peer-reviewedGenomics