Author

Ksenia Khelik

University of Oslo

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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Bioinformatics· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alexander J. NederbragtiD· 2 shared Geir Kjetil SandveiD· 2 shared Torbjørn RognesiD· 2 shared

Activity by Year

2018-2020 · peak 1/yr

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3 top collaborators · 3 mutual co-author links

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2 shared papersBioinformatics

Alexander J. NederbragtORCID

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2 papers

Recent·Most cited

BioinformaticsBMC BioinformaticsPeer-reviewedFeb 21, 2020

NucBreak: Location of structural errors in a genome assembly by using paired-end Illumina reads

Ksenia Khelik, Geir Kjetil Sandve, Alexander J. Nederbragt, Torbjørn Rognes

NucBreak detects structural errors in genome assemblies using paired-end Illumina reads, showing high sensitivity and precision compared to existing tools.

9 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky

BioinformaticsbioRxivPreprintNov 30, 2018

NucMerge: Genome assembly quality improvement assisted by alternative assemblies and paired-end Illumina reads

Ksenia Khelik, Alexander J. Nederbragt, Geir Kjetil Sandve, Torbjørn Rognes

NucMerge improves genome assembly accuracy by integrating alternative assemblies and paired-end Illumina reads, outperforming existing tools in error correction and rearrangement detection.

DOI 10.1101/483701

whole-genome sequencingexperimental assay

𝕏 PostBluesky