Author

Balthasar Clemens Schlotmann

University of CopenhagenORCID 0000-0002-8137-544XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:optimal transport· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Joachim WeischenfeldtiD· 2 shared Alan Rabinowitz· 1 shared Alessio LocalloiD· 1 shared Anne M. HaegertiD· 1 shared Claudio ZanettiniiD· 1 shared Colin C. CollinsiD· 1 shared Colin S. CooperiD· 1 shared Eddie L. ImadaiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersBioinformatics

Joachim WeischenfeldtORCID

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2 papers

Recent·Most cited

BioinformaticsbioRxivPreprintSep 4, 2026

QuickSeg: A fast, versatile and accurate algorithm for genomic copy number segmentation using dynamic programming

Balthasar Clemens Schlotmann, Francesco Favero, Alessio Locallo, Joachim Weischenfeldt

QuickSeg improves copy number segmentation accuracy and efficiency using dynamic programming and median-based error function in cancer whole-genome sequencing data.

DOI 10.64898/2026.08.31.747916

whole-genome sequencingstatistical model

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Genetic & Genomic MedicinemedRxivPreprintApr 28, 2025

Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype Study

Yen‐Yi Lin, Hamideh Sharifi Noghabi, Stanislav V. Volik…·Colin C. Collins

This study identifies rare germline variants associated with metastatic prostate cancer using an extreme phenotype cohort and validates their functional impact.

1 citation

humanwhole-exome sequencing

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