Author

Ola Myklebost

Oslo University HospitalORCID 0000-0002-2866-3223Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:variant calling· 3 Assay:whole-exome sequencing· 3 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Approach:experimental assay· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Eivind J. HovigiD· 3 shared Sigve NakkeniD· 3 shared Daniel VodákiD· 2 shared Lars Birger Aasheim· 2 shared Baoyan BaiiD· 1 shared Ghislain Fournous· 1 shared Harald HolteiD· 1 shared Leonardo A. Meza‐ZepedaiD· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 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

3 shared papersBioinformatics

Eivind J. HovigORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioinformaticsInternational Journal of CancerPeer-reviewedJul 26, 2021

Cancer Predisposition Sequencing Reporter (CPSR): a flexible variant report engine for high-throughput germline screening in cancer

Sigve Nakken, Vladislav Saveliev, Oliver Hofmann…·Eivind J. Hovig

CPSR generates structured reports of germline variants in cancer predisposition genes using ACMG criteria, with customizable gene panels and actionable findings.

21 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsScientific ReportsPeer-reviewedMar 28, 2018

Sample-Index Misassignment Impacts Tumor Exome Sequencing

Daniel Vodák, Susanne Lorenz, Sigve Nakken…·Eivind J. Hovig

The paper shows that sample-index misassignment in tumor exome sequencing can create false somatic variant calls and recommends dual indexing to prevent this.

20 citations

whole-exome sequencingexperimental assay

𝕏 PostBluesky

BioinformaticsBioinformaticsPeer-reviewedDec 19, 2017

Personal Cancer Genome Reporter: Variant Interpretation Report For Precision Oncology

Sigve Nakken, Ghislain Fournous, Daniel Vodák…·Eivind J. Hovig

The paper introduces a tool for interpreting cancer genomes by generating prioritized variant reports for clinical use.

73 citations

humanwhole-exome sequencing

𝕏 PostBluesky