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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 Research, 40 (Database-Issue): 935-939 (2012)

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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 Research, 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. Clinical Bioinformatics, (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. Bioinformatics, 22 (17): 2183-2185 (2006)Performance Analysis of a Parallel, Multi-node Pipeline for DNA Sequencing.D. Decap, J. Reumers, C. Herzeel, P. Costanza, and J. Fostier. PPAM (2), volume 9574 of Lecture Notes in Computer Science, page 233-242. Springer, (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 Research, 40 (Database-Issue): 935-939 (2012)Halvade: scalable sequence analysis with MapReduce.D. Decap, J. Reumers, C. Herzeel, P. Costanza, and J. Fostier. Bioinformatics, 31 (15): 2482-2488 (2015)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. Bioinformatics, 31 (1): 94-101 (2015)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 Bioinformatics, (2015)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 Bioinformatics, 18 (1): 273:1-273:14 (2017)Pipit: visualizing functional impacts of structural variations.R. Sakai, M. Moisse, J. Reumers, and J. Aerts. Bioinformatics, 29 (17): 2206-2207 (2013)

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SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.

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copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.

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SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.