Article

AnoniMME: Bringing Anonymity to the Matchmaker Exchange Platform for Rare Disease Gene Discovery

2018-04-11

Abstract excerpt

<h4>Motivation</h4> Advances in genome sequencing and genomics research are bringing us closer to a new era of personalized medicine, where healthcare can be tailored to the individual’s genetic makeup, and to more effective diagnosis and treatment of rare genetic diseases. Much of this progress depends on collaborations and access to data, thus, a number of initiatives have been introduced to support seamless da...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 10be7cf5-5401-54ae-9353-0b8ae4103a4f
DOI: 10.1101/262295

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

AnoniMME: Bringing Anonymity to the Matchmaker Exchange Platform for Rare Disease Gene DiscoveryDOI 10.1101/262295Read

AnoniMME: bringing anonymity to the Matchmaker Exchange platform for rare disease gene discovery.Semantic proximity Read

The Matchmaker Exchange: a platform for rare disease gene discovery.Semantic proximity Read

Record Linkage based Patient Intersection Cardinality for Rare Disease Studies using Mainzelliste and Secure Multi-Party ComputationSemantic proximity Read

Truly Privacy-Preserving Federated Analytics for Precision Medicine with Multiparty Homomorphic EncryptionSemantic proximity Read

FedGMMAT: Federated Generalized Linear Mixed Model Association TestsSemantic proximity Read

SVAT: Secure Outsourcing of Variant Annotation and Genotype AggregationSemantic proximity Read

The Matchmaker Exchange API: automating patient matching through the exchange of structured phenotypic and genotypic profiles.Semantic proximity Read

SVAT: Secure outsourcing of variant annotation and genotype aggregation.Semantic proximity Read

A novel privacy-preserving federated genome-wide association study framework and its application in identifying potential risk variants in ankylosing spondylitis.Semantic proximity Read

Private detection of relatives in forensic genomics using homomorphic encryption.Semantic proximity Read

Matchmaker Exchange.Semantic proximity Read

De-anonymizing Genomic Databases Using Phenotypic TraitsSemantic proximity Read