Joke Reumers

Orcid: 0000-0001-5434-6515

According to our database1, Joke Reumers authored at least 18 papers between 2003 and 2017.

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Bibliography

2017
A random effects model for the identification of differential splicing (REIDS) using exon and HTA arrays.
BMC Bioinform., 2017

2015
ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clustering.
BMC Bioinform., 2015

QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles.
BMC Bioinform., 2015

VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filtering.
Bioinform., 2015

Halvade: scalable sequence analysis with MapReduce.
Bioinform., 2015

Performance Analysis of a Parallel, Multi-node Pipeline for DNA Sequencing.
Proceedings of the Parallel Processing and Applied Mathematics, 2015

2013
Pipit: visualizing functional impacts of structural variations.
Bioinform., 2013

2012
SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.
Nucleic Acids Res., 2012

Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection.
J. Clin. Bioinform., 2012

2011
An Evolutionary Trade-Off between Protein Turnover Rate and Protein Aggregation Favors a Higher Aggregation Propensity in Fast Degrading Proteins.
PLoS Comput. Biol., 2011

2010
PepX: a structural database of non-redundant protein-peptide complexes.
Nucleic Acids Res., 2010

2009
Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations.
BMC Bioinform., 2009

2008
Reconstruction of Protein Backbones from the BriX Collection of Canonical Protein Fragments.
PLoS Comput. Biol., 2008

Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.
Nucleic Acids Res., 2008

2006
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes.
Nucleic Acids Res., 2006

SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.
Bioinform., 2006

2005
SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs.
Nucleic Acids Res., 2005

2003
Identifiability of Causal Effects in a Multi-Agent Causal Model.
Proceedings of the 2003 IEEE/WIC International Conference on Intelligent Agent Technology (IAT 2003), 2003


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