Author

Svenja Mehringer

Freie Universität Berlin

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 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:database / resource· 1 Organism:human· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Enrico SeileriD· 2 shared Knut ReinertiD· 2 shared Mitra DarvishiD· 2 shared Aðalbjörg Jónasdóttir· 1 shared Agnar HelgasoniD· 1 shared Áslaug Jónasdóttir· 1 shared Ásmundur OddssoniD· 1 shared Bjarni A. AtlasoniD· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersBioinformatics

Enrico SeilerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Hierarchical Interleaved Bloom Filter: Enabling ultrafast, approximate sequence queries

Svenja Mehringer, Enrico Seiler, Felix Droop, Mitra Darvish, René Rahn, Martin Vingron, Knut Reinert

This paper introduces HIBF, a fast and space-efficient data structure for approximate sequence queries, showing significant improvements in speed and resource usage over existing tools.

Genome biology · May 31, 2023Peer-reviewedBioinformatics

Raptor: A fast and space-efficient pre-filter for querying very large collections of nucleotide sequences

Enrico Seiler, Svenja Mehringer, Mitra Darvish, Etienne Turc, Knut Reinert

Raptor is a fast and memory-efficient tool for searching large nucleotide sequence collections, outperforming existing tools in speed and memory usage.

iScience · Jun 24, 2021Peer-reviewedBioinformatics

Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, Hannes P. Eggertsson, Eyþór Björnsson, Hákon Jónsson, Bjarni A. Atlason, Snædís Kristmundsdóttir, Svenja Mehringer, Marteinn Thor Hardarson, Sigurjon Axel Gudjonsson, Droplaug N. Magnúsdóttir, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ragnar P. Kristjansson, , Kāri Stefánsson

The paper uses long-read sequencing on 3,622 Icelanders to identify structural variants and their associations with diseases and traits.

Nature Genetics · May 10, 2021Peer-reviewedGenetics