Author

Magnus Lindell

Uppsala 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

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Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:genome assembly· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam AmeuriD· 1 shared Christian Natanaelsson· 1 shared Helena Fällmar· 1 shared Jessica NordlundiD· 1 shared Johannes AlnebergiD· 1 shared Julia HauensteiniD· 1 shared Pär Lundin· 1 shared Pontus HöjeriD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Adam AmeurORCID

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1 paper

Recent·Most cited

Whole genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases

Pontus Höjer, Johannes Alneberg, Pär Lundin, Tom Martin, Julia Hauenstein, Helena Fällmar, Magnus Lindell, Christian Natanaelsson, Susana Häggqvist, Adam Ameur, Jessica Nordlund, Robert Månsson Welinder

The paper compares variant calling performance between Illumina NovaSeq X Plus and Element AVITI sequencing platforms using whole genome sequencing of human tumor cell lines, finding comparable results with minor differences in specific genomic contexts.

NAR Genomics and Bioinformatics · Mar 27, 2026Peer-reviewedGenomics