Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability

BACKGROUND: The etiology of more than half of all patients with X-linked intellectual disability remains elusive, despite array-based comparative genomic hybridization, whole exome or genome sequencing. Since short read massive parallel sequencing approaches do not allow the detection of larger tand...

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Detalles Bibliográficos
Autores principales: Zablotskaya, Alena, Van Esch, Hilde, Verstrepen, Kevin J., Froyen, Guy, Vermeesch, Joris R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299999/
https://www.ncbi.nlm.nih.gov/pubmed/30567555
http://dx.doi.org/10.1186/s12920-018-0446-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299999/
https://www.ncbi.nlm.nih.gov/pubmed/30567555
http://dx.doi.org/10.1186/s12920-018-0446-7

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