Efficient privacy-preserving whole-genome variant queries

MOTIVATION: Diagnosis and treatment decisions on genomic data have become widespread as the cost of genome sequencing decreases gradually. In this context, disease–gene association studies are of great importance. However, genomic data are very sensitive when compared to other data types and contain...

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Detalles Bibliográficos
Autores principales: Akgün, Mete, Pfeifer, Nico, Kohlbacher, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004657/
https://www.ncbi.nlm.nih.gov/pubmed/35150254
http://dx.doi.org/10.1093/bioinformatics/btac070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004657/
https://www.ncbi.nlm.nih.gov/pubmed/35150254
http://dx.doi.org/10.1093/bioinformatics/btac070

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