Article

SVAT: Secure Outsourcing of Variant Annotation and Genotype Aggregation

2021-09-30

Abstract excerpt

<h4>Background</h4> Sequencing of thousands of samples provides genetic variants with allele frequencies spanning a very large spectrum and gives invaluable insight for genetic determinants of diseases. Protecting the genetic privacy of participants is challenging as only a few rare variants can easily re-identify an individual among millions. In certain cases, there are policy barriers against sharing genetic da...

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Literature Corpus work: a2d99539-3080-5a4b-a69c-b8887517faa4
DOI: 10.1101/2021.09.28.462259

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