Author

Mattias Frånberg

Primary ORCID profile (0000-0002-0749-9903 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Mattias FrånbergiD1 paper · Karolinska University Hospital

Biology Disciplines

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Bioinformatics· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:genome assembly· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Kristoffer SahliniD· 2 shared Lars ArvestadiD· 2 shared

Activity by Year

2015-2017 · peak 1/yr

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2 top collaborators · 1 mutual co-author link

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2 shared papersBioinformatics

Kristoffer SahlinORCID

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2 papers

Recent·Most cited

BioinformaticsJournal of Computational BiologyPeer-reviewedJun 1, 2017

Structural variation detection with read pair information --- An improved null-hypothesis reduces bias

Kristoffer Sahlin, Mattias Frånberg, Lars Arvestad

The paper improves structural variation detection by introducing a more accurate null hypothesis, reducing false positives and correcting a bias in variant calling.

DOI 10.1089/cmb.2016.0124

whole-genome sequencingstatistical model

𝕏 PostBluesky

BioinformaticsbioRxivPreprintAug 4, 2015

Correcting bias from stochastic insert size in read pair data — applications to structural variation detection and genome assembly

Kristoffer Sahlin, Mattias Frånberg, Lars Arvestad

DOI 10.1101/023929

whole-genome sequencingstatistical model

𝕏 PostBluesky