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Author Details
Full Name
Geir Kjetil Sandve
Affiliation
University of Oslo
ORCID
Career Start Year
2006
Papers
76
H Index
23
Expertise
CM4AI Collaborator
Nathan Sheffield (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36696493
Identification of gluten T cell epitopes driving celiac disease.
Sci Adv
2023
37802917
Adjustment of spurious correlations in co-expression measurements from RNA-Sequencing data.
Bioinformatics
2023
37875799
ANDA: an open-source tool for automated image analysis of in vitro neuronal cells.
BMC Neurosci
2023
37058511
DagSim: Combining DAG-based model structure with unconstrained data types and relations for flexible, transparent, and modularized data simulation.
PLoS One
2023
37147306
Effects of prenatal exposure to (es)citalopram and maternal depression during pregnancy on DNA methylation and child neurodevelopment.
Transl Psychiatry
2023
37408750
Artificial intelligence-driven prediction of COVID-19-related hospitalization and death: a systematic review.
Front Public Health
2023
37467208
hGSuite HyperBrowser: A web-based toolkit for hierarchical metadata-informed analysis of genomic tracks.
PLoS One
2023
37162841
ANDA: An open-source tool for automated image analysis of neuronal differentiation.
bioRxiv
2023
35062022
TCRpower: quantifying the detection power of T-cell receptor sequencing with a novel computational pipeline calibrated by spike-in sequences.
Brief Bioinform
2022
37848619
simAIRR: simulation of adaptive immune repertoires with realistic receptor sequence sharing for benchmarking of immune state prediction methods.
Gigascience
2022
35377271
In silico proof of principle of machine learning-based antibody design at unconstrained scale.
MAbs
2022
35765087
Low reliability of DNA methylation across Illumina Infinium platforms in cord blood: implications for replication studies and meta-analyses of prenatal exposures.
Clin Epigenetics
2022
35639633
Profiling the baseline performance and limits of machine learning models for adaptive immune receptor repertoire classification.
Gigascience
2022
35852318
CompAIRR: ultra-fast comparison of adaptive immune receptor repertoires by exact and approximate sequence matching.
Bioinformatics
2022
36046619
Reference-based comparison of adaptive immune receptor repertoires.
Cell Rep Methods
2022
36073940
Access to ground truth at unconstrained size makes simulated data as indispensable as experimental data for bioinformatics methods development and benchmarking.
Bioinformatics
2022
36195962
KAGE: fast alignment-free graph-based genotyping of SNPs and short indels.
Genome Biol
2022
33197618
T cell receptor repertoire as a potential diagnostic marker for celiac disease.
Clin Immunol
2021
33574832
Editorial: Genomic Colocalization and Enrichment Analyses.
Front Genet
2021
33903675
Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB.
Sci Rep
2021
33927715
Comprehensive Analysis of CDR3 Sequences in Gluten-Specific T-Cell Receptors Reveals a Dominant R-Motif and Several New Minor Motifs.
Front Immunol
2021
33730590
A compact vocabulary of paratope-epitope interactions enables predictability of antibody-antigen binding.
Cell Rep
2021
33705383
Ten simple rules for quick and dirty scientific programming.
PLoS Comput Biol
2021
34815307
Individualized VDJ recombination predisposes the available Ig sequence space.
Genome Res
2021
34618841
Differential expression profile of gluten-specific T cells identified by single-cell RNA-seq.
PLoS One
2021
31624847
Beware the Jaccard: the choice of similarity measure is important and non-trivial in genomic colocalisation analysis.
Brief Bioinform
2020
32085722
NucBreak: location of structural errors in a genome assembly by using paired-end Illumina reads.
BMC Bioinformatics
2020
31727780
B cell tolerance and antibody production to the celiac disease autoantigen transglutaminase 2.
J Exp Med
2020
32094913
Author Correction: Human somatic cell mutagenesis creates genetically tractable sarcomas.
Nat Genet
2020
32154832
immuneSIM: tunable multi-feature simulation of B- and T-cell receptor repertoires for immunoinformatics benchmarking.
Bioinformatics
2020
32252628
Assessing graph-based read mappers against a baseline approach highlights strengths and weaknesses of current methods.
BMC Genomics
2020
30307532
Colocalization analyses of genomic elements: approaches, recommendations and challenges.
Bioinformatics
2019
31839965
Transcriptional profiling of human intestinal plasma cells reveals effector functions beyond antibody production.
United European Gastroenterol J
2019
31251803
A map of direct TF-DNA interactions in the human genome.
Nucleic Acids Res
2019
30779737
Graph Peak Caller: Calling ChIP-seq peaks on graph-based reference genomes.
PLoS Comput Biol
2019
30517703
A map of direct TF-DNA interactions in the human genome.
Nucleic Acids Res
2019
29757191
Disease-driving CD4+ T cell clonotypes persist for decades in celiac disease.
J Clin Invest
2018
29873782
Coloc-stats: a unified web interface to perform colocalization analysis of genomic features.
Nucleic Acids Res
2018
30547739
Mind the gaps: overlooking inaccessible regions confounds statistical testing in genome analysis.
BMC Bioinformatics
2018
30517183
Exploiting antigen receptor information to quantify index switching in single-cell transcriptome sequencing experiments.
PLoS One
2018
28521741
The rainfall plot: its motivation, characteristics and pitfalls.
BMC Bioinformatics
2017
28459977
GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome.
Gigascience
2017
29284043
Complex patterns of concomitant medication use: A study among Norwegian women using paracetamol during pregnancy.
PLoS One
2017
28600290
High-Throughput Single-Cell Analysis of B Cell Receptor Usage among Autoantigen-Specific Plasma Cells in Celiac Disease.
J Immunol
2017
28701187
NucDiff: in-depth characterization and annotation of differences between two sets of DNA sequences.
BMC Bioinformatics
2017
28911336
Genome build information is an essential part of genomic track files.
Genome Biol
2017
28775312
Uracil Accumulation and Mutagenesis Dominated by Cytosine Deamination in CpG Dinucleotides in Mice Lacking UNG and SMUG1.
Sci Rep
2017
28521770
Coordinates and intervals in graph-based reference genomes.
BMC Bioinformatics
2017
26819474
Galaxy Portal: interacting with the galaxy platform through mobile devices.
Bioinformatics
2016
26586731
In the loop: promoter-enhancer interactions and bioinformatics.
Brief Bioinform
2016
1 - 50 of 76
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Collaborators
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Center for Bioinformatics, University of Oslo
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NTNU - Norwegian University of Science and Technology
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11
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University of Oslo
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University of Oslo
Co-authored papers
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Co-authored papers
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University of Mainz
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University of Oslo
Co-authored papers
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Co-authored papers
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CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
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Daniel Vod??k
Institute for Cancer Research, Oslo University Hospital
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2
Ryan M Layer
Boulder and BioFrontiers Institute, University of Colorado Boulder
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2
Carsten O Daub
International Institute of Molecular and Cell Biology in Warsaw
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1
Sigve Nakken
University of Oslo
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1
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RIKEN Center for Integrative Medical Sciences
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