Author

Morten Källberg

Illumina (United Kingdom)

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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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Organism:human· 1

Frequent Co-Authors

Aaron L. HalperniD· 1 shared Alexey Dolgoborodov· 1 shared Amit JainiD· 1 shared Andrew L. StachyraiD· 1 shared Berke Ç. Toptaş· 1 shared Björn Pollex· 1 shared Christopher T. SaundersiD· 1 shared Deniz KuraliD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBioinformatics

Aaron L. HalpernORCID

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2 papers

Recent·Most cited

BioinformaticsNature GeneticsPeer-reviewedJan 9, 2019

Fast and Accurate Genomic Analyses using Genome Graphs

Goran Rakocevic, Vladimir Semenyuk, Wan‐Ping Lee…·Deniz Kural

This paper introduces a graph genome reference that improves read alignment and variant calling accuracy compared to traditional haplotype-based methods.

222 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

BioinformaticsNature MethodsPeer-reviewedJul 11, 2018

Strelka2: Fast and accurate variant calling for clinical sequencing applications

Sangtae Kim, Konrad Scheffler, Aaron L. Halpern…·Christopher T. Saunders

Strelka2 is a variant calling tool that improves accuracy and reduces compute cost for germline and somatic variant detection in clinical sequencing.

1,642 citationstop 1%

whole-genome sequencingstatistical model

𝕏 PostBluesky