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

B. Verbist, K. Thys, J. Reumers, Y. Wetzels, K. der Borght, W. Talloen, J. Aerssens, L. Clement, and O. Thas. Bioinform., 31 (1): 94-101 (2015)

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Hennric Jokeit

Gabriele Jokeit

Thomas Jokerst

Joke Pöstges

Joke Schubach

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PepX: a structural database of non-redundant protein-peptide complexes.P. Vanhee, J. Reumers, F. Stricher, L. Baeten, L. Serrano, J. Schymkowitz, and F. Rousseau. Nucleic Acids Res., 38 (Database-Issue): 545-551 (2010)Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection.A. Stubbs, E. McClellan, S. Horsman, S. Hiltemann, I. Palli, S. Nouwens, A. Koning, F. Hoogland, J. Reumers, D. Heijsman and 5 other author(s). J. Clin. Bioinform., (2012)SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.J. Reumers, S. Maurer-Stroh, J. Schymkowitz, and F. Rousseau. Bioinform., 22 (17): 2183-2185 (2006)VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filtering.B. Verbist, K. Thys, J. Reumers, Y. Wetzels, K. der Borght, W. Talloen, J. Aerssens, L. Clement, and O. Thas. Bioinform., 31 (1): 94-101 (2015)SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.G. Baets, J. van Durme, J. Reumers, S. Maurer-Stroh, P. Vanhee, J. Dopazo, J. Schymkowitz, and F. Rousseau. Nucleic Acids Res., 40 (Database-Issue): 935-939 (2012)Pipit: visualizing functional impacts of structural variations.R. Sakai, M. Moisse, J. Reumers, and J. Aerts. Bioinform., 29 (17): 2206-2207 (2013)ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clustering.B. Verbist, L. Clement, J. Reumers, K. Thys, A. Vapirev, W. Talloen, Y. Wetzels, J. Meys, J. Aerssens, L. Bijnens and 1 other author(s). BMC Bioinform., (2015)Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.J. Reumers, L. Conde, I. Medina, S. Maurer-Stroh, J. van Durme, J. Dopazo, F. Rousseau, and J. Schymkowitz. Nucleic Acids Res., 36 (Database-Issue): 825-829 (2008)A random effects model for the identification of differential splicing (REIDS) using exon and HTA arrays.M. Moerbeke, A. Kasim, W. Talloen, J. Reumers, H. Göhlmann, and Z. Shkedy. BMC Bioinform., 18 (1): 273:1-273:14 (2017)Reconstruction of Protein Backbones from the BriX Collection of Canonical Protein Fragments.L. Baeten, J. Reumers, V. Tur, F. Stricher, T. Lenaerts, L. Serrano, F. Rousseau, and J. Schymkowitz. PLoS Comput. Biol., (2008)

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Disambiguation of "Reumers, Joke"

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

Please choose a person to relate this publication to

Hennric Jokeit

Gabriele Jokeit

Thomas Jokerst

Joke Pöstges

Joke Schubach

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Reumers, Joke"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filtering.

Please choose a person to relate this publication to

Hennric Jokeit

Gabriele Jokeit

Thomas Jokerst

Joke Pöstges

Joke Schubach

Other publications of authors with the same name

Disambiguation

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URL
DOI
BibTeX
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VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filtering.