Author

Maria Rossing

Copenhagen University HospitalORCID 0000-0003-4325-3027Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:batch correction / integration· 1 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Approach:statistical model· 1

Frequent Co-Authors

Christina Bligaard PederseniD· 2 shared Frederik Otzen BaggeriD· 2 shared Lars Rønn OlseniD· 2 shared Arman SimonyaniD· 1 shared Benito CamposiD· 1 shared Binay PandaiD· 1 shared Christina Westmose YdeiD· 1 shared Filipe Garrett VieiraiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersBioinformatics

Christina Bligaard PedersenORCID

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2 papers

Recent·Most cited

BioinformaticsMolecular OncologyPeer-reviewedDec 30, 2023

Building flexible and robust analysis frameworks for molecular subtyping of cancers

Christina Bligaard Pedersen, Benito Campos, Lasse Rene…·Lars Rønn Olsen

The paper provides a framework for molecular cancer subtyping that integrates quality control, normalization, batch correction, classification, and reporting, with a use case in breast cancer.

4 citations

humanbulk RNA-seq

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BioinformaticsCancersPeer-reviewedDec 14, 2021

A comparison of tools for copy-number variation detection in germline whole exome and whole genome sequencing data

Miglė Gabrielaitė, Mathias Husted Torp, Malthe Sebro Rasmussen…·Frederik Otzen Bagger

The paper benchmarks CNV detection tools on WGS and WES data using clinical standards and reference samples, finding that combining multiple tools improves recall but precision remains a challenge.

111 citationstop 1%

humanwhole-exome sequencing

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