Evidence map›Paper›PMID 31366927›Full record

ArticleScientific reports2019

LEI: A Novel Allele Frequency-Based Feature Selection Method for Multi-ancestry Admixed Populations.

Michael J Wathen, Yadu Gautam, Sudhir Ghandikota, Marepalli B Rao, Tesfaye B Mersha

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

1 citing paper in PubMed, 14 citations in OpenAlex.

  1. 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 at 2 institutions in 1 country.

Michael J WathenDivision of Biostatistics and Epidemiology, University of Cincinnati, Cincinnati, OH, 45229, USA.
Yadu GautamDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, 45229, USA.
Sudhir GhandikotaDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, 45229, USA.
Marepalli B RaoDivision of Biostatistics and Epidemiology, University of Cincinnati, Cincinnati, OH, 45229, USA.
Tesfaye B MershaDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, 45229, USA. tesfaye.mersha@cchmc.org.
University of Cincinnati · USCincinnati Children's Hospital Medical Center · US

Funding

Unraveling ancestry and environmental exposure interactions in childhood asthmaR01HL132344 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI MERSHA, TESFAYE B. · 2016 to 2020
$3.4M
Ancestry-Environmental Exposure Interactions and Asthma Risk in Admixed PopulationR03HL133713 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI MERSHA, TESFAYE B. · 2016 to 2017
$156k
NHLBI NIH HHS R01 HL132344NHLBI NIH HHS R03 HL133713
6 · The paper itself

Abstract

Next-generation sequencing technologies now make it possible to sequence and genotype hundreds of thousands of genetic markers across the human genome. Selection of informative markers for the comprehensive characterization of individual genomic makeup using a high dimensional genomics dataset has become a common practice in evolutionary biology and human genetics. Although several feature selection approaches exist to determine the ancestry proportion in two-way admixed populations including African Americans, there are limited statistical tools developed for the feature selection approaches in three-way admixed populations (including Latino populations). Herein, we present a new likelihood-based feature selection method called Lancaster Estimator of Independence (LEI) that utilizes allele frequency information to prioritize the most informative features useful to determine ancestry proportion from multiple ancestral populations in admixed individuals. The ability of LEI to leverage summary-level statistics from allele frequency data, thereby avoiding the many restrictions (and big data issues) that can accompany access to individual-level genotype data, is appealing to minimize the computation and time-consuming ancestry inference in an admixed population. We compared our allele-frequency based approach with genotype-based approach in estimating admixed proportions in three-way admixed population scenarios. Our results showed ancestry estimates using the top-ranked features from LEI were comparable with the estimates using features from genotype-based methods in three-way admixed population. We provide an easy-to-use R code to assist researchers in using the LEI tool to develop allele frequency-based informative features to conduct admixture mapping studies from mixed samples of multiple ancestry origin.

Indexed as

Gene FrequencyGenetic MarkersGenetics, PopulationGenome, HumanGenomicsGenotypeHumansLikelihood FunctionsSoftwareGenetic Markers

Identifiers

PMID31366927
PMCPMC6668412
OpenAlexW2965327025

What OpenQuestion holds

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LicenceCC BY
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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.