Author

Johan Dahlberg

Uppsala UniversityORCID 0000-0001-6962-1460Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioengineering· 1 Bioinformatics· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:database / resource· 2 Organism:human· 2 Assay:whole-genome sequencing· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:proteomics· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Adam AmeuriD· 2 shared Francesco VezziiD· 2 shared Huiwen CheiD· 2 shared Lars FeukiD· 2 shared Marcel MartiniD· 2 shared Pall I. OlasoniD· 2 shared Ulf B GyllensteniD· 2 shared Álvaro Martínez BarrioiD· 1 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Adam AmeurORCID

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4 papers

Recent·Most cited

BioengineeringbioRxivPreprintJun 19, 2025

Cells as Single-Molecule Protein Proximity Networks

Filip Karlsson, Michele Simonetti, Christina Galonska…·Simon Fredriksson

The paper introduces PNA, a DNA-based method to map protein organization and interactions in single cells, revealing abundance, clustering, and colocalization relationships.

3 citations

proteomicsexperimental assay

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BioinformaticsGigaSciencePeer-reviewedDec 1, 2019

Arteria: An automation system for a sequencing core facility

Johan Dahlberg, Johan Hermansson, Steinar Sturlaugsson…·Pontus Larsson

Arteria provides an automation system for sequencing core facilities using modular, open-source micro-services.

5 citations

experimental assaysoftware / tool

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GenomicsGenesPeer-reviewedOct 9, 2018

De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data

Adam Ameur, Huiwen Che, Marcel Martin…·Ulf B Gyllensten

The paper performs de novo assembly of two Swedish genomes, identifies novel sequences absent from GRCh38, and shows improved variant calling with these sequences.

58 citations

humanwhole-genome sequencing

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GeneticsEuropean Journal of Human GeneticsPeer-reviewedAug 23, 2017

SweGen: A whole-genome map of genetic variability in a cross-section of the Swedish population

Adam Ameur, Johan Dahlberg, Pall I. Olason…·Ulf B Gyllensten

SweGen provides a high-quality whole-genome map of genetic variation in the Swedish population, useful for clinical genetics and association studies.

209 citationstop 1%

humanwhole-genome sequencing

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