Author

Lars Birger Aasheim

Oslo University Hospital

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

Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Daniel VodákiD· 2 shared Eivind J. HovigiD· 2 shared Ola MyklebostiD· 2 shared Sigve NakkeniD· 2 shared Baoyan BaiiD· 1 shared Ghislain Fournous· 1 shared Harald HolteiD· 1 shared Leonardo A. Meza‐ZepedaiD· 1 shared

Activity by Year

2017-2018 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 32 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

2 shared papersGenomics

Daniel VodákORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Sample-Index Misassignment Impacts Tumor Exome Sequencing

Daniel Vodák, Susanne Lorenz, Sigve Nakken, Lars Birger Aasheim, Harald Holte, Baoyan Bai, Ola Myklebost, Leonardo A. Meza‐Zepeda, 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.

Scientific Reports · Mar 28, 2018Peer-reviewedGenomics

Personal Cancer Genome Reporter: Variant Interpretation Report For Precision Oncology

Sigve Nakken, Ghislain Fournous, Daniel Vodák, Lars Birger Aasheim, Ola Myklebost, Eivind J. Hovig

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

Bioinformatics · Dec 19, 2017Peer-reviewedBioinformatics