Evidence map›Paper›PMID 29977040›Full record

ArticleScientific reports2018

Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference.

Consuelo D Quinto-Cortés, August E Woerner, Joseph C Watkins, Michael F Hammer

Abstract read
In one paragraph

Article in Scientific reports, 2018. 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

The trial behind it

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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

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

4 authors.

Consuelo D Quinto-CortésNational Laboratory of Genomics for Biodiversity (LANGEBIO), CINVESTAV, Irapuato, 36821, Mexico, Mexico. consuelo.quinto@cinvestav.mx.
August E WoernerCenter for Human Identification, University of North Texas Health Science Center, Texas, 76107, USA.
Joseph C WatkinsDepartment of Mathematics, University of Arizona, Tucson, Arizona, 85721, USA.
Michael F HammerARL Division of Biotechnology, University of Arizona, Tucson, Arizona, 85721, USA. mfh@email.arizona.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) in commercial arrays have often been discovered in a small number of samples from selected populations. This ascertainment skews patterns of nucleotide diversity and affects population genetic inferences. We propose a demographic inference pipeline that explicitly models the SNP discovery protocol in an Approximate Bayesian Computation (ABC) framework. We simulated genomic regions according to a demographic model incorporating parameters for the divergence of three well-characterized HapMap populations and recreated the SNP distribution of a commercial array by varying the number of haploid samples and the allele frequency cut-off in the given regions. We then calculated summary statistics obtained from both the ascertained and genomic data and inferred ascertainment and demographic parameters. We implemented our pipeline to study the admixture process that gave rise to the present-day Mexican population. Our estimate of the time of admixture is closer to the historical dates than those in previous works which did not consider ascertainment bias. Although the use of whole genome sequences for demographic inference is becoming the norm, there are still underrepresented areas of the world from where only SNP array data are available. Our inference framework is applicable to those cases and will help with the demographic inference.

Indexed as

Polymorphism, Single NucleotideAfrica, WesternAsian PeopleBayes TheoremBlack or African AmericanBlack PeopleChinaHumansModels, GeneticUtahWhite PeopleWhole Genome Sequencing

Identifiers

PMID29977040
PMCPMC6033855

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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.