2022
DOI: 10.1093/bioinformatics/btac070
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Efficient privacy-preserving whole-genome variant queries

Abstract: 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 is very sensitive when compared to other data types and contains information about individuals and their relatives. Many studies have shown that this information can be obtained from the query-response pairs on genomic databases. In this work, we propose a metho… Show more

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Cited by 7 publications
(3 citation statements)
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“…Sequence reads were visualized by Bio Edit Sequence Alignment Editor software (Alzohairy, 2011). Sequences with noisy data background were trimmed and introduced to the BiQ analyzer software which displays the methylated sites and unmethylated sites separately (Akgün et al, 2022).…”
Section: Quantification Of Gene Expressionmentioning
confidence: 99%
“…Sequence reads were visualized by Bio Edit Sequence Alignment Editor software (Alzohairy, 2011). Sequences with noisy data background were trimmed and introduced to the BiQ analyzer software which displays the methylated sites and unmethylated sites separately (Akgün et al, 2022).…”
Section: Quantification Of Gene Expressionmentioning
confidence: 99%
“…In biomedicine, this approach has been applied in several important applications to prevent data leakage. For example, a federated solution based on the secure multi-party computation was proposed for whole-genome variant-querying ( Akgun et al , 2022 ), and the identification of disease-associated variants ( Akgun et al , 2021 ) by combing multiple distributed genomic data resources. Another work ( Zolotareva et al , 2021 ) explored the possibility of the federated learning approach for differential gene expression analysis of multiple resources and highlighted its utility with regard to its robustness against class imbalance.…”
Section: Introductionmentioning
confidence: 99%
“…The program Bio Edit Sequence Alignment Editor was used to view the sequence readings (28). After being trimmed, sequences with noisy data backgrounds were sent into the BiQ analyzer program, which shows the methylation and unmethylated sites independently(29).…”
mentioning
confidence: 99%