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Joke Reumers

Showing results (21-30 of 41) with videos related to

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Bioinformatics (Oxford, England)|September 3, 2014
VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filteringBie M P Verbist, Kim Thys, Joke Reumers, et al.
BMC Bioinformatics|April 19, 2015
ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clusteringBie Verbist, Lieven Clement, Joke Reumers, et al.
Nature Medicine|April 30, 2024
Microbiome confounders and quantitative profiling challenge predicted microbial targets in colorectal cancer developmentRaúl Y Tito, Sara Verbandt, Marta Aguirre Vazquez, et al.
Human Mutation|April 11, 2008
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson diseaseVeerle Bogaerts, Karen Nuytemans, Joke Reumers, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2023
Transcription factor expression repertoire basis for epigenetic and transcriptional subtypes of colorectal cancersYuba R Bhandari, Vinod Krishna, Rachael Powers, et al.
Human Molecular Genetics|February 21, 2012
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisSarah Herdewyn, Hui Zhao, Matthieu Moisse, et al.
Nature Chemical Biology|March 30, 2011
Gain of function of mutant p53 by coaggregation with multiple tumor suppressorsJie Xu, Joke Reumers, José R Couceiro, et al.
Nature Methods|February 16, 2010
Exploring the sequence determinants of amyloid structure using position-specific scoring matricesSebastian Maurer-Stroh, Maja Debulpaep, Nico Kuemmerer, et al.
The Lancet. Oncology|May 22, 2012
VEGF pathway genetic variants as biomarkers of treatment outcome with bevacizumab: an analysis of data from the AViTA and AVOREN randomised trialsDiether Lambrechts, Bart Claes, Paul Delmar, et al.
Elife|August 3, 2014
Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaksHui Zhao, Bernard Thienpont, Betül Tuba Yesilyurt, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Bioinformatics (Oxford, England)|September 3, 2014
VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filteringBie M P Verbist, Kim Thys, Joke Reumers, et al.
BMC Bioinformatics|April 19, 2015
ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clusteringBie Verbist, Lieven Clement, Joke Reumers, et al.
Nature Medicine|April 30, 2024
Microbiome confounders and quantitative profiling challenge predicted microbial targets in colorectal cancer developmentRaúl Y Tito, Sara Verbandt, Marta Aguirre Vazquez, et al.
Human Mutation|April 11, 2008
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson diseaseVeerle Bogaerts, Karen Nuytemans, Joke Reumers, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2023
Transcription factor expression repertoire basis for epigenetic and transcriptional subtypes of colorectal cancersYuba R Bhandari, Vinod Krishna, Rachael Powers, et al.
Human Molecular Genetics|February 21, 2012
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisSarah Herdewyn, Hui Zhao, Matthieu Moisse, et al.
Nature Chemical Biology|March 30, 2011
Gain of function of mutant p53 by coaggregation with multiple tumor suppressorsJie Xu, Joke Reumers, José R Couceiro, et al.
Nature Methods|February 16, 2010
Exploring the sequence determinants of amyloid structure using position-specific scoring matricesSebastian Maurer-Stroh, Maja Debulpaep, Nico Kuemmerer, et al.
The Lancet. Oncology|May 22, 2012
VEGF pathway genetic variants as biomarkers of treatment outcome with bevacizumab: an analysis of data from the AViTA and AVOREN randomised trialsDiether Lambrechts, Bart Claes, Paul Delmar, et al.
Elife|August 3, 2014
Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaksHui Zhao, Bernard Thienpont, Betül Tuba Yesilyurt, et al.
Pageof 5