Evidence map›Paper›PMID 34600465›Full record

ArticleBMC genomics2021

Privacy-preserving storage of sequenced genomic data.

Rastislav Hekel, Jaroslav Budis, Marcel Kucharik, Jan Radvanszky, Zuzana Pös, Tomas Szemes

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Methods for safely sharing dual-use genetic data.Frontiers in microbiology · 2026
    Article
  2. Article
  3. The Multi-Omic Approach to Newborn Screening: Opportunities and Challenges.International journal of neonatal screening · 2024
    Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Rastislav HekelGeneton s.r.o, Bratislava, Slovakia. rastislav.hekel@geneton.sk.ORCID http://orcid.org/0000-0003-1623-9537
Jaroslav BudisGeneton s.r.o, Bratislava, Slovakia.
Marcel KucharikGeneton s.r.o, Bratislava, Slovakia.
Jan RadvanszkyGeneton s.r.o, Bratislava, Slovakia.
Zuzana PösGeneton s.r.o, Bratislava, Slovakia.
Tomas SzemesGeneton s.r.o, Bratislava, Slovakia.
Geneton (Slovakia) · SKBiomedical Research Center of the Slovak Academy of Sciences · SK

Funding

European Regional Development Fund 26240220071European Regional Development Fund 313011V578European Regional Development Fund NFP313010Q927OP Integrated Infrastructure for the project Center for biomedical research 313011W428
6 · The paper itself

Abstract

backgroundThe current and future applications of genomic data may raise ethical and privacy concerns. Processing and storing of this data introduce a risk of abuse by potential offenders since the human genome contains sensitive personal information. For this reason, we have developed a privacy-preserving method, named Varlock providing secure storage of sequenced genomic data. We used a public set of population allele frequencies to mask the personal alleles detected in genomic reads. Each personal allele described by the public set is masked by a randomly selected population allele with respect to its frequency. Masked alleles are preserved in an encrypted confidential file that can be shared in whole or in part using public-key cryptography.

resultsOur method masked the personal variants and introduced new variants detected in a personal masked genome. Alternative alleles with lower population frequency were masked and introduced more often. We performed a joint PCA analysis of personal and masked VCFs, showing that the VCFs between the two groups cannot be trivially mapped. Moreover, the method is reversible and personal alleles in specific genomic regions can be unmasked on demand.

conclusionOur method masks personal alleles within genomic reads while preserving valuable non-sensitive properties of sequenced DNA fragments for further research. Personal alleles in the desired genomic regions may be restored and shared with patients, clinics, and researchers. We suggest that the method can provide an additional security layer for storing and sharing of the raw aligned reads.

Indexed as

GenomicsPrivacyAllelesGene FrequencyGenome, HumanHumansGenomic privacyGenomic readsPersonal data

Identifiers

PMID34600465
PMCPMC8487550
OpenAlexW3203106615

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.