Frontiers in Genetics (Sep 2022)
Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases
- Zirui Dong,
- Zirui Dong,
- Zirui Dong,
- Zirui Dong,
- Dezso David,
- Claudia Gonzaga-Jauregui,
- Cynthia C. Morton,
- Cynthia C. Morton,
- Cynthia C. Morton,
- Cynthia C. Morton,
- Cynthia C. Morton,
- Cinthya J. Zepeda-Mendoza
Affiliations
- Zirui Dong
- Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong SAR, China
- Zirui Dong
- Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China
- Zirui Dong
- Hong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong SAR, China
- Zirui Dong
- Department of Obstetrics and Gynaecology, The Fertility Preservation Research Center, The Chinese University of Hong Kong, Hong Kong SAR, China
- Dezso David
- Department of Human Genetics, National Health Institute Doutor Ricardo Jorge, Lisbon, Portugal
- Claudia Gonzaga-Jauregui
- International Laboratory for Human Genome Research, Laboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, Mexico
- Cynthia C. Morton
- Department of Obstetrics and Gynecology, Brigham and Women’s Hospital, Boston, MA, United States
- Cynthia C. Morton
- Department of Pathology, Brigham and Women’s Hospital, Boston, MA, United States
- Cynthia C. Morton
- Harvard Medical School, Boston, MA, United States
- Cynthia C. Morton
- 0Broad Institute of MIT and Harvard, Cambridge, MA, United States
- Cynthia C. Morton
- 1Manchester Centre for Audiology and Deafness, School of Health Sciences, University of Manchester, Manchester, United Kingdom
- Cinthya J. Zepeda-Mendoza
- 2Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States
- DOI
- https://doi.org/10.3389/fgene.2022.1022918
- Journal volume & issue
-
Vol. 13
Abstract
No abstracts available.Keywords
- structural variant (SV)
- methodologies & tools
- SV spectrum
- sequence complexity
- annotation and prediction
- genomic variation