Author

Siegfried Schloissnig

Research Institute of Molecular PathologyORCID 0000-0003-4574-8330Unclaimed ORCID profile · follow to get notified of new preprints

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Siegfried Schloissnig1 paper

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Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

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Arda SöyleviD· 1 shared Bernardo Rodríguez–MartíniD· 1 shared Carsten HainiD· 1 shared Christian GilisseniD· 1 shared Dagmar WieczorekiD· 1 shared Ewan BirneyiD· 1 shared Francy J. Pérez-LlanosiD· 1 shared Hufsah AshrafiD· 1 shared

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2025-2025 · peak 1/yr

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Arda SöylevORCID

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1 paper

Recent·Most cited

GenomicsNaturePeer-reviewedJul 23, 2025

Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project

Siegfried Schloissnig, Samarendra Pani, Jana Ebler…·Jan O. Korbel

The paper uses long-read sequencing to characterize structural variants in 1,019 samples from the 1000 Genomes Project, identifying 167,291 sequence-resolved SVs and highlighting their genomic and functional implications.

121 citationstop 1%

humanwhole-genome sequencing

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