Author

Sascha Meiers

European Molecular Biology LaboratoryORCID 0000-0003-2609-0000Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ashley D. SandersiD· 2 shared David PorubskỳiD· 2 shared Jan O. KorbeliD· 2 shared Tobias MarschalliD· 2 shared Tobias RauschiD· 2 shared Aaron M. WengeriD· 1 shared Adrian M. StütziD· 1 shared Alex R. HastieiD· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Ashley D. SandersORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintNov 21, 2019

Single cell tri-channel-processing reveals structural variation landscapes and complex rearrangement processes

Ashley D. Sanders, Sascha Meiers, Maryam Ghareghani…·Jan O. Korbel

This paper introduces scTRIP, a method to detect structural variations in single cells, revealing new SV classes and mutational processes in cancer samples.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsNature CommunicationsPeer-reviewedApr 16, 2019

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Mark Chaisson, Ashley D. Sanders, Xuefang Zhao…·Charles Lee

This study identifies a large number of structural variants in human genomes using multiple sequencing technologies and presents them as a gold standard for future studies.

889 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky