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Article

Assessing and mitigating privacy risks of sparse, noisy genotypes by local alignment to haplotype databases.

Genome research - 27 Dec 2023

Emani Prashant S, Geradi Maya N, Gürsoy Gamze, Grasty Monica R, Miranker Andrew, Gerstein Mark B

Abstract excerpt

Single nucleotide polymorphisms (SNPs) from omics data create a reidentification risk for individuals and their relatives. Although the ability of thousands of SNPs (especially rare ones) to identify individuals has been repeatedly shown, the availability of small sets of noisy genotypes, from environmental DNA samples or functional genomics data, motivated us to quantify their informativeness. We present a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 38097386
DOI: 10.1101/gr.278322.123
PMCID: PMC10760520

Provenance

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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