Author

Eric Minwei Liu

Aarhus University HospitalORCID 0000-0002-3594-6678Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:gene regulatory network inference· 3 Assay:whole-genome sequencing· 3 Research Focus:database / resource· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1

Frequent Co-Authors

Abdullah KahramaniD· 3 shared Abel González-PéreziD· 3 shared André KahlesiD· 3 shared Andrés LanzósiD· 3 shared Asger HobolthiD· 3 shared Benjamin J. RaphaeliD· 3 shared Calvin Wing Yiu ChaniD· 3 shared Carl HerrmanniD· 3 shared

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2017-2020 · peak 3/yr

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10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Abdullah KahramanORCID

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4 papers

Recent·Most cited

BioinformaticsPLoS ONEPeer-reviewedNov 2, 2020

NetBoxR: Automated Discovery of Biological Process Modules by Network Analysis in R

Eric Minwei Liu, Augustin Luna, Guanlan Dong, Chris Sander

NetBoxR identifies cancer-related biological processes using network analysis, combining multiple data types to find functional modules without relying on curated gene sets.

10 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsCommunications BiologyPeer-reviewedFeb 5, 2020

Unique genomic features and deeply-conserved functions of long non-coding RNAs in the Cancer LncRNA Census (CLC)

Joana Carlevaro-Fita, Andrés Lanzós, Lars Feuerbach…·S. Cenk Şahinalp

The paper introduces the Cancer LncRNA Census (CLC), a curated resource of lncRNAs with causative roles in cancer, and shows their genomic and evolutionary features.

189 citationstop 1%

humanmouse

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BioinformaticsNature CommunicationsPeer-reviewedFeb 5, 2020

Integrative pathway enrichment analysis of multivariate omics data

Marta Paczkowska, Jonathan Barenboim, Nardnisa Sintupisut…·Leonidas Salichos

ActivePathways integrates multivariate omics data to identify enriched pathways, revealing cancer driver genes and prognostic pathways in breast cancer.

223 citationstop 1%

humanwhole-genome sequencing

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GenomicsbioRxivPreprintDec 23, 2017

Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes

Esther Rheinbay, Morten Muhlig Nielsen, Federico Abascal…·Gad A. Getz

The paper identifies and characterizes coding and non-coding driver mutations across 2,500 cancer genomes, revealing new candidates and questioning previous findings.

40 citations

humanwhole-genome sequencing

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