Cargando…
Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data
Mosaic genetic variants can have major clinical impact. We systematically analyse trio exome sequence data from 4,293 probands from the DDD Study with severe developmental disorders for pathogenic postzygotic mosaicism (PZM) in the child or a clinically-unaffected parent, and use ultrahigh-depth seq...
Autores principales: | Wright, C. F., Prigmore, E., Rajan, D., Handsaker, J., McRae, J., Kaplanis, J., Fitzgerald, T. W., FitzPatrick, D. R., Firth, H. V., Hurles, M. E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611863/ https://www.ncbi.nlm.nih.gov/pubmed/31278258 http://dx.doi.org/10.1038/s41467-019-11059-2 |
Ejemplares similares
-
Author Correction: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data
por: Wright, C. F., et al.
Publicado: (2022) -
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutations
por: Kaplanis, Joanna, et al.
Publicado: (2019) -
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders
por: Gardner, Eugene J., et al.
Publicado: (2021) -
MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples
por: Huang, August Yue, et al.
Publicado: (2017) -
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1133 families with developmental disorders
por: Wright, Caroline F., et al.
Publicado: (2018)