Evidence map›Paper›PMID 27995319›Full record

ArticleInternational journal of legal medicine2017

Prediction of biogeographical ancestry from genotype: a comparison of classifiers.

Elaine Y Y Cheung, Michelle Elizabeth Gahan, Dennis McNevin

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Article in International journal of legal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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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

3 authors.

Elaine Y Y CheungNational Centre for Forensic Studies, Faculty of Education, Science, Technology & Mathematics (ESTeM), University of Canberra, Bruce, ACT 2601, Australia. Elaine.Cheung@canberra.edu.au.
Michelle Elizabeth GahanNational Centre for Forensic Studies, Faculty of Education, Science, Technology & Mathematics (ESTeM), University of Canberra, Bruce, ACT 2601, Australia.
Dennis McNevinNational Centre for Forensic Studies, Faculty of Education, Science, Technology & Mathematics (ESTeM), University of Canberra, Bruce, ACT 2601, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA can provide forensic intelligence regarding a donor's biogeographical ancestry (BGA) and other externally visible characteristics (EVCs). A number of algorithms have been proposed to assign individual human genotypes to a BGA using ancestry informative marker (AIM) panels. This study compares the BGA assignment accuracy of the population clustering program STRUCTURE and three generic classification approaches including a Bayesian algorithm, genetic distance, and multinomial logistic regression (MLR). A selection of 142 ancestry informative single nucleotide polymorphisms (SNPs) were chosen from existing marker panels (SNPforID 34-plex, Eurasiaplex, Seldin, and Kidd's AIM panels) to assess BGA classification at the continental level for Africans, Europeans, East Asians, and Amerindians. A training set of 1093 individuals with self-declared BGA from the 1000 Genomes phase 1 database was used by each classifier to predict BGA in a test set of 516 individuals from the HGDP-CEPH (Stanford) cell line panel. Tests were repeated with 0, 10, 50, 70, and 90% of the genotypes missing. Comparison of the area under the receiver operating characteristic curves (AUROCs) showed high accuracy in STRUCTURE and the generic Bayesian approach. The latter algorithm offers a computationally simpler alternative to STRUCTURE with little loss in accuracy and is suitable for phenotype prediction while STRUCTURE is not.

Indexed as

GenotypeAlgorithmsGenealogy and HeraldryGene FrequencyGenetic MarkersHumansLikelihood FunctionsLogistic ModelsPolymorphism, Single NucleotideRacial GroupsGenetic MarkersBayesianBiogeographical ancestry (BGA)Genetic distanceMultinomial logistic regressionPhenotype predictionSTRUCTURE

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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.