Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples
Robin Wijngaard(Radboud University Nijmegen), Christian Gilissen(Radboud University Nijmegen), Rolph Pfundt(Radboud University Nijmegen), Amber den Ouden(Radboud University Nijmegen), Volker Straub(Newcastle upon Tyne Hospitals NHS Foundation Trust), Laurence Faivre(Inserm), Richarda M. de Voer(Radboud University Nijmegen), Lisenka E.L.M. Vissers(Radboud University Nijmegen), Clarissa Rocca(Institute of Human Genetics), Iris te Paske(Radboud University Nijmegen), Anneke J. van der Kooi(Amsterdam UMC Location University of Amsterdam), Jana Vandrovcová(Texas Tech University), Antonio Vitobello(Inserm), Hilde Swinkels(Radboud University Nijmegen), Wouter Steyaert(Ghent University Hospital), Ana Töpf(NIHR Newcastle Biomedical Research Centre), Elke de Boer(Radboud University Nijmegen), Luke O’Gorman(Radboud University Nijmegen), Anne‐Sophie Denommé‐Pichon(Inserm), Steven Laurie(Centre for Genomic Regulation), Erik‐Jan Kamsteeg(Radboud University Nijmegen), Stephan Ossowski(University of Southern California), Martin Chevarin(Inserm), Francesca Magrinelli(National Hospital for Neurology and Neurosurgery), Jordi Corominas‐Galbany(Radboud University Nijmegen), Yannis Duffourd(CHU Dijon Bourgogne), German Demidov(Universitat Pompeu Fabra), Burcu Yaldız(Radboud University Nijmegen), Michael G. Hanna(National Hospital for Neurology and Neurosurgery)
Cited by 2
Related Papers
Ensembl 2012
|Nucleic Acids Research|2011|839
Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences
|Briefings in Bioinformatics|2016|815
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing
|Science Translational Medicine|2017|809