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Article

SVAT: Secure outsourcing of variant annotation and genotype aggregation.

BMC bioinformatics - 1 Oct 2022

Kim Miran, Wang Su, Jiang Xiaoqian, Harmanci Arif

Abstract excerpt

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-identify an individual among millions. In certain cases, there are policy barriers against sharing genetic data from...

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Identifiers

PMID: 36182914
DOI: 10.1186/s12859-022-04959-6
PMCID: PMC9526274

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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