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Uncovering the complexity of structural variants in four individuals with autism spectrum disorder.

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第一作者： Sarah,Dada

第一单位： Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.;BC Children's Hospial Research Institute, Vancouver, BC, Canada.;Department of Bioinformatics, Faculty of Science, University of British Columbia, Vancouver, BC, Canada.

作者： Sarah,Dada ^[1] ; Katherine,Dixon ^[2] ; Vahid,Akbari ^[2] ; Cameron J,Grisdale ^[3] ; Kristina,Calli ^[4] ; Sally,Martell ^[4] ; Caralyn,Reisle ^[5] ; Amanda,Lillico-Ouachour ^[4] ; M E Suzanne,Lewis ^[4] ; Steven J M,Jones ^[6]

作者单位： Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.;BC Children's Hospial Research Institute, Vancouver, BC, Canada.;Department of Bioinformatics, Faculty of Science, University of British Columbia, Vancouver, BC, Canada. ^[1] Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.;Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada. ^[2] Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada. ^[3] BC Children's Hospial Research Institute, Vancouver, BC, Canada.;Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada. ^[4] Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.;Department of Bioinformatics, Faculty of Science, University of British Columbia, Vancouver, BC, Canada. ^[5] Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.;Department of Bioinformatics, Faculty of Science, University of British Columbia, Vancouver, BC, Canada.;Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada. ^[6]

关键词 autism spectrum disorder clinical genetics complex structural variants nanopore long-read sequencing whole-genome sequencing