Evidence map›Paper›PMID 28507140›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Linkage disequilibrium matches forensic genetic records to disjoint genomic marker sets.

Michael D Edge, Bridget F B Algee-Hewitt, Trevor J Pemberton, Jun Z Li, Noah A Rosenberg

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Toward minimal SNP sets for record-matching with CODIS STR profiles.European journal of human genetics : EJHG · 2026
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  4. Review
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  6. Article
  7. Review
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  12. Record-matching of STR profiles with fragmentary genomic SNP data.European journal of human genetics : EJHG · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Associations between forensic loci and expression levels of neighboring genes may compromise medical privacy.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Review
  18. Article
  19. Article
  20. DNA Data Collection and Analysis in the Forensic Arena.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
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

5 authors.

Michael D EdgeDepartment of Biology, Stanford University, Stanford, CA 94305.
Bridget F B Algee-HewittDepartment of Biology, Stanford University, Stanford, CA 94305.
Trevor J PembertonDepartment of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB, Canada R3E0J9.
Jun Z LiDepartment of Human Genetics, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-6727-0812
Noah A RosenbergDepartment of Biology, Stanford University, Stanford, CA 94305; noahr@stanford.edu.

Funding

Population genetics for large-scale sequencing studies of diverse populationsR01HG005855 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Noah Rosenberg, Paul A Scheet · 2010 to 2026
$5.8M
NHGRI NIH HHS R01 HG005855
6 · The paper itself

Abstract

Combining genotypes across datasets is central in facilitating advances in genetics. Data aggregation efforts often face the challenge of record matching-the identification of dataset entries that represent the same individual. We show that records can be matched across genotype datasets that have no shared markers based on linkage disequilibrium between loci appearing in different datasets. Using two datasets for the same 872 people-one with 642,563 genome-wide SNPs and the other with 13 short tandem repeats (STRs) used in forensic applications-we find that 90-98% of forensic STR records can be connected to corresponding SNP records and vice versa. Accuracy increases to 99-100% when ∼30 STRs are used. Our method expands the potential of data aggregation, but it also suggests privacy risks intrinsic in maintenance of databases containing even small numbers of markers-including databases of forensic significance.

Indexed as

Data CollectionForensic GeneticsGenetic MarkersGenome, HumanGenomicsHumansLinkage DisequilibriumMicrosatellite RepeatsPolymorphism, Single NucleotideGenetic Markersforensic DNAgenomic privacyimputationpopulation geneticsrecord matching

Identifiers

PMID28507140
PMCPMC5465933

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Registered trials

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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.