Blar i Bergen Open Research Archive på forfatter "Lavrichenko, Ksenia"
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Comprehensive characterization of copy number variation (CNV) called from array, long- and short-read data
Lavrichenko, Ksenia; Johansson, Stefan; Jonassen, Inge (Journal article; Peer reviewed, 2021)Background SNP arrays, short- and long-read genome sequencing are genome-wide high-throughput technologies that may be used to assay copy number variants (CNVs) in a personal genome. Each of these technologies comes with ... -
The Flow of Quasiconformal Mappings on S³ with Contact structure and a Family of Surfaces on the Heisenberg Group
Lavrichenko, Ksenia (Master thesis, 2011-05-31) -
Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents
Smajlagic, Dinka; Lavrichenko, Ksenia; Berland, Siren; Helgeland, Øyvind; Knudsen, Gun Peggy Strømstad; Vaudel, Marc; Haavik, Jan; Knappskog, Per; Njølstad, Pål Rasmus; Houge, Gunnar; Johansson, Stefan (Journal article; Peer reviewed, 2020)Recurrent copy number variations (CNVs) are common causes of neurodevelopmental disorders (NDDs) and associated with a range of psychiatric traits. These CNVs occur at defined genomic regions that are particularly prone ... -
SeeCiTe: a method to assess CNV calls from SNP arrays using trio data
Lavrichenko, Ksenia; Helgeland, Øyvind; Njølstad, Pål Rasmus; Jonassen, Inge; Johansson, Stefan (Journal article; Peer reviewed, 2021)Motivation Single nucleotide polymorphism (SNP) genotyping arrays remain an attractive platform for assaying copy number variants (CNVs) in large population-wide cohorts. However, current tools for calling CNVs are still ...