Evidence map›Paper›PMID 30033616›Full record

ArticleMolecular ecology resources2018

SNP-skimming: A fast approach to map loci generating quantitative variation in natural populations.

Carolyn A Wessinger, John K Kelly, Peng Jiang, Mark D Rausher, Lena C Hileman

Abstract read
In one paragraph

Article in Molecular ecology resources, 2018. 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
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Rapid floral syndrome convergence inbioRxiv : the preprint server for biology · 2026
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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

5 authors at 2 institutions in 1 country.

Carolyn A WessingerDepartment of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas.ORCID http://orcid.org/0000-0003-3687-2559
John K KellyDepartment of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas.
Peng JiangDepartment of Biology, Duke University, Durham, North Carolina.
Mark D RausherDepartment of Biology, Duke University, Durham, North Carolina.
Lena C HilemanDepartment of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas.
University of Kansas · USDuke University · US

Funding

Understanding the mechanobiology of stem cells in a microengineered 3D cardiac tissue environment with cardiomyopathyP20GM103638 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI LUNTE, SUSAN M · 2012 to 2021
$22.1M
Genomic Analysis of Complex Trait Variation in MimulusR01GM073990 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI KELLY, JOHN K · 2006 to 2015
$2.6M
The genetic and developmental basis of repeated phenotypic shifts in PenstemonF32GM110988 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI WESSINGER, CARRIE · 2014 to 2016
$164k
National Institutes of Health F32 GM110988-3National Institutes of Health R01 GM073990-02National Science Foundation DEB-1542402NIGMS NIH HHS F32 GM110988NIGMS NIH HHS P20 GM103638NIGMS NIH HHS R01 GM073990
6 · The paper itself

Abstract

Genome-wide association mapping (GWAS) is a method to estimate the contribution of segregating genetic loci to trait variation. A major challenge for applying GWAS to nonmodel species has been generating dense genome-wide markers that satisfy the key requirement that marker data are error-free. Here, we present an approach to map loci within natural populations using inexpensive shallow genome sequencing. This "SNP-skimming" approach involves two steps: an initial genome-wide scan to identify putative targets followed by deep sequencing for confirmation of targeted loci. We apply our method to a test data set of floral dimension variation in the plant Penstemon virgatus, a member of a genus that has experienced dynamic floral adaptation that reflects repeated transitions in primary pollinator. The ability to detect SNPs that generate phenotypic variation depends on population genetic factors such as population allele frequency, effect size and epistasis, as well as sampling effects contingent on missing data and genotype uncertainty. However, both simulations and the Penstemon data suggest that the most significant tests from the initial SNP skim are likely to be true positives-loci with subtle but significant quantitative effects on phenotype. We discuss the promise and limitations of this method and consider optimal experimental design for a given sequencing effort. Simulations demonstrate that sampling a larger number of individual at the expense of average read depth per individual maximizes the power to detect loci.

Indexed as

Polymorphism, Single NucleotideFlowersGenome-Wide Association StudyGenotypeHigh-Throughput Nucleotide SequencingPenstemonPhenotypeSequence Analysis, DNAGWASmultiplexed shotgun genotypingPenstemonquantitative trait loci

Identifiers

PMID30033616
PMCPMC6207453
OpenAlexW2884651525

What OpenQuestion holds

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Registered trials

None linked

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.