檢索結果 - Joris Vermeesch

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  1. 1
    Genomic microarrays: a technology overview

    Genomic microarrays: a technology overview 由 Paul Brady, Joris Vermeesch

    出版 2012
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  2. 2
    Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics

    Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics 由 Simon Ardui, Adam Ameur, Joris Vermeesch, Matthew S. Hestand

    出版 2018
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  3. 3
    A benchmark of structural variation detection by long reads through a realistic simulated model

    A benchmark of structural variation detection by long reads through a realistic simulated model 由 Nicolas Dierckxsens, Tong Li, Joris Vermeesch, Zhi Xie

    出版 2021
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  4. 4
    Diagnosis of miscarriages by molecular karyotyping: Benefits and pitfalls

    Diagnosis of miscarriages by molecular karyotyping: Benefits and pitfalls 由 Caroline Robberecht, Vicky Schuddinck, Jean‐Pierre Fryns, Joris Vermeesch

    出版 2009
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  5. 5
    Polymerase specific error rates and profiles identified by single molecule sequencing

    Polymerase specific error rates and profiles identified by single molecule sequencing 由 Matthew S. Hestand, Jeroen Van Houdt, Francesca Cristofoli, Joris Vermeesch

    出版 2016
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  6. 6
    GBSX: a toolkit for experimental design and demultiplexing genotyping by sequencing experiments

    GBSX: a toolkit for experimental design and demultiplexing genotyping by sequencing experiments 由 Koen Herten, Matthew S. Hestand, Joris Vermeesch, Jeroen KJ Van Houdt

    出版 2015
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  7. 7
    Preimplantation genetic diagnosis guided by single-cell genomics

    Preimplantation genetic diagnosis guided by single-cell genomics 由 Niels van der Aa, Masoud Zamani Esteki, Joris Vermeesch, Thierry Voet

    出版 2013
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  8. 8
    Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores

    Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores 由 Maria Siermann, Ophelia Valcke, Joris Vermeesch, Taneli Raivio, Olga Tšuiko, Pascal Borry

    出版 2023
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  9. 9
    BinDel: Detecting Clinically Relevant Fetal Genomic Microdeletions Using Low‐Coverage Whole‐Genome Sequencing‐Based NIPT

    BinDel: Detecting Clinically Relevant Fetal Genomic Microdeletions Using Low‐Coverage Whole‐Genome Sequencing‐Based NIPT 由 Priit Paluoja, Tatjana Jatsenko, Hindrek Teder, Kaarel Krjutškov, Joris Vermeesch, Andres Salumets, Priit Palta

    出版 2025
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  10. 10
    Molecular genetics of 22q11.2 deletion syndrome

    Molecular genetics of 22q11.2 deletion syndrome 由 Bernice E. Morrow, Donna M. McDonald‐McGinn, Beverly S. Emanuel, Joris Vermeesch, Peter Scambler

    出版 2018
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  11. 11
    Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane

    Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane 由 Cosimo De Bari, Francesco Dell’Accio, Frank Vandenabeele, Joris Vermeesch, Jean‐Marc Raymackers, Frank P. Luyten

    出版 2003
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  12. 12
    Large-scale analysis of tandem repeat variability in the human genome

    Large-scale analysis of tandem repeat variability in the human genome 由 Jorge Duitama, Alena Zablotskaya, Rita Gemayel, An Jansen, Stefanie Belet, Joris Vermeesch, Kevin J. Verstrepen, Guy Froyen

    出版 2014
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  13. 13
    Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection

    Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection 由 Tine De Coster, Yan Zhao, Olga Tšuiko, S. Demyda‐Peyrás, Ann Van Soom, Joris Vermeesch, Katrien Smits

    出版 2024
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  14. 14
    Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions

    Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions 由 Hannelie M. Engbers, Jasper J. van der Smagt, Ruben van ‘t Slot, Joris Vermeesch, Ron Hochstenbach, Martin Poot

    出版 2008
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  15. 15
    Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos

    Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos 由 Afroditi Mertzanidou, L. Wilton, Jun‐Hu Cheng, Claudia Spits, Evelyne Vanneste, Yves Moreau, Joris Vermeesch, Karen Sermon

    出版 2012
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  16. 16
    Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing

    Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing 由 Simon Ardui, Valérie Race, Alena Zablotskaya, Matthew S. Hestand, Hilde Van Esch, Koenraad Devriendt, Gert Matthijs, Joris Vermeesch

    出版 2016
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  17. 17
    Large deletions of the APC gene in 15% of mutation‐negative patients with classical polyposis (FAP): A Belgian study

    Large deletions of the APC gene in 15% of mutation‐negative patients with classical polyposis (FAP): A Belgian study 由 G Michils, Sabine Tejpar, Ronald Thoelen, Eric Van Cutsem, Joris Vermeesch, Jean‐Pierre Fryns, Eric Legius, Gert Matthijs

    出版 2005
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  18. 18
    Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation

    Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation 由 Kasper Gadsbøll, Olav Bjørn Petersen, Vincent Gâtinois, Heather Strange, Bo Jacobsson, Ronald J. Wapner, Joris Vermeesch, Ida Vogel

    出版 2020
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  19. 19
    Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome

    Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome 由 Pawandeep Dhami, Alison J. Coffey, Stephen Abbs, Joris Vermeesch, Jan P. Dumanski, Karen Woodward, Robert Andrews, Cordelia Langford, David Vetrie

    出版 2005
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  20. 20
    Glypican-6, a New Member of the Glypican Family of Cell Surface Heparan Sulfate Proteoglycans

    Glypican-6, a New Member of the Glypican Family of Cell Surface Heparan Sulfate Proteoglycans 由 Mark Veugelers, Bart De Cat, Helga Ceulemans, Anne-Marie Bruystens, Christien Coomans, Joachim Dürr, Joris Vermeesch, Peter Marynen, Guido David

    出版 1999
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