SVAT: Secure outsourcing of variant annotation and genotype aggregation

BACKGROUND: Sequencing of thousands of samples provides genetic variants with allele frequencies spanning a very large spectrum and gives invaluable insight into genetic determinants of diseases. Protecting the genetic privacy of participants is challenging as only a few rare variants can easily re-...

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Detalles Bibliográficos
Autores principales: Kim, Miran, Wang, Su, Jiang, Xiaoqian, Harmanci, Arif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526274/
https://www.ncbi.nlm.nih.gov/pubmed/36182914
http://dx.doi.org/10.1186/s12859-022-04959-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526274/
https://www.ncbi.nlm.nih.gov/pubmed/36182914
http://dx.doi.org/10.1186/s12859-022-04959-6

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