Cargando…
Whole genome prediction for preimplantation genetic diagnosis
BACKGROUND: Preimplantation genetic diagnosis (PGD) enables profiling of embryos for genetic disorders prior to implantation. The majority of PGD testing is restricted in the scope of variants assayed or by the availability of extended family members. While recent advances in single cell sequencing...
Autores principales: | Kumar, Akash, Ryan, Allison, Kitzman, Jacob O, Wemmer, Nina, Snyder, Matthew W, Sigurjonsson, Styrmir, Lee, Choli, Banjevic, Milena, Zarutskie, Paul W, Lewis, Alexandra P, Shendure, Jay, Rabinowitz, Matthew |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445980/ https://www.ncbi.nlm.nih.gov/pubmed/26019723 http://dx.doi.org/10.1186/s13073-015-0160-4 |
Ejemplares similares
-
Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development
por: McCoy, Rajiv C., et al.
Publicado: (2015) -
Whole-genome risk prediction of common diseases in human preimplantation embryos
por: Kumar, Akash, et al.
Publicado: (2022) -
Informatics-based, highly accurate, noninvasive prenatal paternity testing
por: Ryan, Allison, et al.
Publicado: (2013) -
Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strains
por: Salipante, Stephen J., et al.
Publicado: (2015) -
Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach
por: Hall, Megan P., et al.
Publicado: (2014)