Editorial: The clinical utility of long read sequencing to improve diagnostic yield and uncover biological mechanisms in rare disease

• Lidia Larizza,
• Christopher M. Watson,
• Christopher M. Watson,
• Madelyn A. Gillentine,
• Palma Finelli,
• Palma Finelli

Affiliations

Lidia Larizza

Research Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy

Christopher M. Watson

Institute of Medical Research, St James’s University Hospital, University of Leeds Faculty of Medicine and Health, Leeds, United Kingdom

Christopher M. Watson

North East and Yorkshire Genomic Laboratory Hub, Central Lab, St James’s University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom

Madelyn A. Gillentine

Department of Laboratories, Seattle Children’s Hospital, Seattle, WA, United States

Palma Finelli

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, University of Milan, Milan, Italy

Palma Finelli

Medical Genetics Laboratory, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy