Evidence map›Paper›PMID 29165562›Full record

ArticleGenome biology and evolution2017

The Diversity of REcent and Ancient huMan (DREAM): A New Microarray for Genetic Anthropology and Genealogy, Forensics, and Personalized Medicine.

Eran Elhaik, Leeban Yusuf, Ainan I J Anderson, Mehdi Pirooznia, Dimitrios Arnellos, Gregory Vilshansky, Gunes Ercal, Yontao Lu, Teresa Webster, Michael L Baird and 1 more

Abstract read
In one paragraph

Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
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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

11 authors.

Eran ElhaikDepartment of Animal and Plant Sciences, University of Sheffield, United Kingdom.
Leeban YusufDepartment of Animal and Plant Sciences, University of Sheffield, United Kingdom.
Ainan I J AndersonIndependent researcher, Newick, United Kingdom.
Mehdi PiroozniaDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University.
Dimitrios ArnellosDepartment of Animal and Plant Sciences, University of Sheffield, United Kingdom.
Gregory VilshanskyNational Geographic Society, Washington, District of Columbia.
Gunes ErcalDepartment of Computer Science, Southern Illinois University Edwardsville.
Yontao LuThermo Fisher Scientific, Santa Clara, California.
Teresa WebsterThermo Fisher Scientific, Santa Clara, California.
Michael L BairdDNA Diagnostics Center, Fairfield, Ohio.
Umberto EspositoDepartment of Animal and Plant Sciences, University of Sheffield, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human population displays wide variety in demographic history, ancestry, content of DNA derived from hominins or ancient populations, adaptation, traits, copy number variation, drug response, and more. These polymorphisms are of broad interest to population geneticists, forensics investigators, and medical professionals. Historically, much of that knowledge was gained from population survey projects. Although many commercial arrays exist for genome-wide single-nucleotide polymorphism genotyping, their design specifications are limited and they do not allow a full exploration of biodiversity. We thereby aimed to design the Diversity of REcent and Ancient huMan (DREAM)-an all-inclusive microarray that would allow both identification of known associations and exploration of standing questions in genetic anthropology, forensics, and personalized medicine. DREAM includes probes to interrogate ancestry informative markers obtained from over 450 human populations, over 200 ancient genomes, and 10 archaic hominins. DREAM can identify 94% and 61% of all known Y and mitochondrial haplogroups, respectively, and was vetted to avoid interrogation of clinically relevant markers. To demonstrate its capabilities, we compared its FST distributions with those of the 1000 Genomes Project and commercial arrays. Although all arrays yielded similarly shaped (inverse J) FST distributions, DREAM's autosomal and X-chromosomal distributions had the highest mean FST, attesting to its ability to discern subpopulations. DREAM performances are further illustrated in biogeographical, identical by descent, and copy number variation analyses. In summary, with approximately 800,000 markers spanning nearly 2,000 genes, DREAM is a useful tool for genetic anthropology, forensic, and personalized medicine studies.

Indexed as

Genome, HumanAnthropologyDNA, AncientDNA Copy Number VariationsEvolution, MolecularGenetic MarkersGenetics, PopulationGenotypeHumansMicroarray AnalysisPedigreePolymorphism, Single NucleotidePrecision MedicineDNA, AncientGenetic Markersancient DNAarchaic DNAbiogeographyCNVsforensicspopulation genetics

Identifiers

PMID29165562
PMCPMC5726468

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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.