Wouter De Coster - VIB, Appl & Translat Neurogen Grp, Ctr Mol Neurol, Antwerp, Belgium

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论文共 37 篇作者统计合作学者相似作者

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Methylmap: Visualization of Modified Nucleotides for Large Cohort Sizes

Elise Coopman, Svenn D’Hert,Rosa Rademakers,Wouter De Coster

BMC Bioinformaticsno. 1 (2025): 1-7

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Increased TMEM106B Levels Lead to Lysosomal Dysfunction Which Affects Synaptic Signaling and Neuronal Health

Jolien Perneel, Miranda Lastra Osua, Sara Alidadiani, Nele Peeters, Linus De Witte,Bavo Heeman, Simona Manzella,Riet De Rycke, Mieu Brooks, Ralph B. Perkerson, Elke Calus,Wouter De Coster,Manuela Neumann,Ian R. A. Mackenzie,Debby Van Dam,Bob Asselbergh,Tommas Ellender,Xiaolai Zhou,Rosa Rademakers

Molecular Neurodegenerationno. 1 (2025): 1-26

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Medically relevant tandem repeats in nanopore sequencing of control cohorts

Wouter De Coster,Ida Höijer, Inge Bruggeman,Svenn D'Hert,Malin Melin,Adam Ameur,Rosa Rademakers

crossref（2024）

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Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes Via Whole-Genome Sequencing

Cyril Pottier,Fahri Küçükali,Matt Baker,Anthony Batzler,Gregory D Jenkins,Marka van Blitterswijk,Cristina T Vicente,Wouter De Coster,Sarah Wynants, Pieter Van de Walle,Owen A Ross,Melissa E Murray,Júlia Faura,Stephen J Haggarty,Jeroen Gj van Rooij,Merel O Mol,Ging-Yuek R Hsiung,Caroline Graff,Linn Öijerstedt,Manuela Neumann,Yan Asmann,Shannon K McDonnell,Saurabh Baheti,Keith A Josephs,Jennifer L Whitwell,Kevin F Bieniek,Leah Forsberg,Hilary Heuer,Argentina Lario Lago,Ethan G Geier,Jennifer S Yokoyama, Alexis P Oddi,Margaret Flanagan,Qinwen Mao,John R Hodges,John B Kwok,Kimiko Domoto-Reilly,Matthis Synofzik,Carlo Wilke,Chiadi Onyike,Bradford C Dickerson,Bret M Evers,Brittany N Dugger,David G Munoz,Julia Keith,Lorne Zinman,Ekaterina Rogaeva,EunRan Suh,Tamar Gefen,Changiz Geula,Sandra Weintraub,Janine Diehl-Schmid,Martin R Farlow,Dieter Edbauer,Bryan K Woodruff,Richard J Caselli, Laura L Donker Kaat,Edward D Huey,Eric M Reiman,Simon Mead,Andrew King,Sigrun Roeber,Alissa L Nana,Nilufer Ertekin-Taner,David S Knopman,Ronald C Petersen,Leonard Petrucelli,Ryan J Uitti,Zbigniew K Wszolek,Eliana Marisa Ramos,Lea T Grinberg,Maria Luisa Gorno Tempini,Howard J Rosen,Salvatore Spina,Olivier Piguet,Murray Grossman,John Q Trojanowski,Dirk C Keene,Jin Lee-Way,Johannes Prudlo,Daniel H Geschwind,Robert A Rissman,Carlos Cruchaga,Bernardino Ghetti,Glenda M Halliday,Thomas G Beach,Geidy E Serrano,Thomas Arzberger,Jochen Herms,Adam L Boxer,Lawrence S Honig,Jean P Vonsattel,Oscar L Lopez,Julia Kofler,Charles L White,Marla Gearing,Jonathan Glass,Jonathan D Rohrer,David J Irwin,Edward B Lee,Vivianna Van Deerlin,Rudolph Castellani,Marsel M Mesulam,Maria C Tartaglia,Elizabeth C Finger,Claire Troakes,Safa Al-Sarraj,Bruce L Miller,Harro Seelaar,Neill R Graff-Radford,Bradley F Boeve,Ian Ra Mackenzie,John C van Swieten,William W Seeley,Kristel Sleegers,Dennis W Dickson,Joanna M Biernacka,Rosa Rademakers

medRxiv the preprint server for health sciences (2024)

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Nanopore Sequencing of 1000 Genomes Project Samples to Build a Comprehensive Catalog of Human Genetic Variation

Jonas A Gustafson,Sophia B Gibson,Nikhita Damaraju,Miranda Pg Zalusky,Kendra Hoekzema,David Twesigomwe,Lei Yang,Anthony A Snead, Phillip A Richmond,Wouter De Coster,Nathan D Olson,Andrea Guarracino, Qiuhui Li,Angela L Miller,Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha,Claudia Gonzaga-Jauregui,Wayne E Clarke,Anna O Basile,André Corvelo,Catherine Reeves,Adrienne Helland,Rajeeva Lochan Musunuri, Mahler Revsine,Karynne E Patterson,Cate R Paschal, Christina Zakarian,Sara Goodwin,Tanner D Jensen, Esther Robb, Genomes ONT Sequencing Consortium, University of Washington Center for Rare Disease Research (UW-CRDR), Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium,W Richard McCombie,Fritz J Sedlazeck,Justin M Zook,Stephen B Montgomery,Erik Garrison,Mikhail Kolmogorov,Michael C Schatz,Richard N McLaughlin,Harriet Dashnow,Michael C Zody,Matt Loose,Miten Jain,Evan E Eichler,Danny E Miller

medRxiv the preprint server for health sciences (2024)

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Analysis and Benchmarking of Small and Large Genomic Variants Across Tandem Repeats

Adam C. English,Egor Dolzhenko,Helyaneh Ziaei Jam,Sean K. Mckenzie,Nathan D. Olson,Wouter De Coster,Jonghun Park,Bida Gu,Justin Wagner,Michael A. Eberle,Melissa Gymrek,Mark J. P. Chaisson,Justin M. Zook,Fritz J. Sedlazeck

NATURE BIOTECHNOLOGY（2024）

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Scywalker: Scalable End-to-end Data Analysis Workflow for Long-Read Single-Cell Transcriptome Sequencing

Peter De Rijk, Tijs Watzeels, Fahri Kuecuekali,Jasper Van Dongen,Julia Faura,Patrick Willems, Lara De Deyn,Lena Duchateau,Carolin Grones,Thomas Eekhout,Tim De Pooter,Geert Joris,Stephane Rombauts,Bert De Rybel,Rosa Rademakers,Frank Van Breusegem,Mojca Strazisar,Kristel Sleegers,Wouter De Coster

BIOINFORMATICSno. 9 (2024)

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High-coverage Nanopore Sequencing of Samples from the 1000 Genomes Project to Build a Comprehensive Catalog of Human Genetic Variation

Jonas A. Gustafson,Sophia B. Gibson,Nikhita Damaraju,Miranda P. G. Zalusky,Kendra Hoekzema,David Twesigomwe, Lei Yang,Anthony A. Snead, Phillip A. Richmond,Wouter De Coster,Nathan D. Olson,Andrea Guarracino, Qiuhui Li,Angela L. Miller,Joy Goffena, Zachary B. Anderson, Sophie H. R. Storz, Sydney A. Ward, Maisha Sinha,Claudia Gonzaga-Jauregui,Wayne E. Clarke,Anna O. Basile,Andre Corvelo,Catherine Reeves,Adrienne Helland,Rajeeva Lochan Musunuri, Mahler Revsine,Karynne E. Patterson,Cate R. Paschal, Christina Zakarian,Sara Goodwin,Tanner D. Jensen, Esther Robb,William Richard McCombie,Fritz J. Sedlazeck,Justin M. Zook,Stephen B. Montgomery,Erik Garrison,Mikhail Kolmogorov,Michael C. Schatz,Richard N. McLaughlin Jr,Harriet Dashnow,Michael C. Zody,Matt Loose,Miten Jain,Evan E. Eichler,Danny E. Miller

GENOME RESEARCHno. 11 (2024): 2061-2073

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Full Characterization of Unresolved Structural Variation Through Long-Read Sequencing and Optical Genome Mapping

Griet De Clercq,Lies Vantomme,Barbara Dewaele,Bert Callewaert,Olivier Vanakker,Sandra Janssens,Bart Loeys,Mojca Strazisar,Wouter De Coster,Joris Robert Vermeesch,Annelies Dheedene,Bjoern Menten

SCIENTIFIC REPORTS（2024）

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Visualization and Analysis of Medically Relevant Tandem Repeats in Nanopore Sequencing of Control Cohorts with Pathstr

Wouter De Coster,Ida Hoijer, Inge Bruggeman,Svenn D'Hert,Malin Melin,Adam Ameur,Rosa Rademakers

GENOME RESEARCH（2024）

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