Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders

Structural variation (SV) describes a broad class of genetic variation greater than 50 bp in size. SVs can cause a wide range of genetic diseases and are prevalent in rare developmental disorders (DDs). Individuals presenting with DDs are often referred for diagnostic testing with chromosomal microa...

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Detalles Bibliográficos
Autores principales: Gardner, Eugene J., Sifrim, Alejandro, Lindsay, Sarah J., Prigmore, Elena, Rajan, Diana, Danecek, Petr, Gallone, Giuseppe, Eberhardt, Ruth Y., Martin, Hilary C., Wright, Caroline F., FitzPatrick, David R., Firth, Helen V., Hurles, Matthew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595893/
https://www.ncbi.nlm.nih.gov/pubmed/34626536
http://dx.doi.org/10.1016/j.ajhg.2021.09.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595893/
https://www.ncbi.nlm.nih.gov/pubmed/34626536
http://dx.doi.org/10.1016/j.ajhg.2021.09.010

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