Evidence map›Paper›PMID 30677030›Full record

ArticlePloS one2019

SNP variable selection by generalized graph domination.

Shuzhen Sun, Zhuqi Miao, Blaise Ratcliffe, Polly Campbell, Bret Pasch, Yousry A El-Kassaby, Balabhaskar Balasundaram, Charles Chen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

8 authors at 4 institutions in 2 countries.

Shuzhen SunDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, United States of America.
Zhuqi MiaoCenter for Health Systems Innovation, Oklahoma State University, Stillwater, United States of America.
Blaise RatcliffeDepartment of Forest and Conservation Sciences, Faculty of Forestry, The University of British Columbia, Vancouver, B.C. Canada.ORCID 0000-0003-4469-2929
Polly CampbellDepartment of Integrative Biology, Oklahoma State University, Stillwater, United States of America.
Bret PaschDepartment of Biological Sciences, Northern Arizona University, Flagstaff, United States of America.
Yousry A El-KassabyDepartment of Forest and Conservation Sciences, Faculty of Forestry, The University of British Columbia, Vancouver, B.C. Canada.
Balabhaskar BalasundaramSchool of Industrial Engineering and Management, Oklahoma State University, Stillwater, United States of America.
Charles ChenDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, United States of America.ORCID 0000-0002-2203-0433
Oklahoma State University · USUniversity of British Columbia · CANorthern Arizona University · USUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-throughput sequencing technology has revolutionized both medical and biological research by generating exceedingly large numbers of genetic variants. The resulting datasets share a number of common characteristics that might lead to poor generalization capacity. Concerns include noise accumulated due to the large number of predictors, sparse information regarding the p≫n problem, and overfitting and model mis-identification resulting from spurious collinearity. Additionally, complex correlation patterns are present among variables. As a consequence, reliable variable selection techniques play a pivotal role in predictive analysis, generalization capability, and robustness in clustering, as well as interpretability of the derived models. METHODS AND

findingsK-dominating set, a parameterized graph-theoretic generalization model, was used to model SNP (single nucleotide polymorphism) data as a similarity network and searched for representative SNP variables. In particular, each SNP was represented as a vertex in the graph, (dis)similarity measures such as correlation coefficients or pairwise linkage disequilibrium were estimated to describe the relationship between each pair of SNPs; a pair of vertices are adjacent, i.e. joined by an edge, if the pairwise similarity measure exceeds a user-specified threshold. A minimum k-dominating set in the SNP graph was then made as the smallest subset such that every SNP that is excluded from the subset has at least k neighbors in the selected ones. The strength of k-dominating set selection in identifying independent variables, and in culling representative variables that are highly correlated with others, was demonstrated by a simulated dataset. The advantages of k-dominating set variable selection were also illustrated in two applications: pedigree reconstruction using SNP profiles of 1,372 Douglas-fir trees, and species delineation for 226 grasshopper mouse samples. A C++ source code that implements SNP-SELECT and uses Gurobi optimization solver for the k-dominating set variable selection is available (https://github.com/transgenomicsosu/SNP-SELECT).

Indexed as

AlgorithmsGenome-Wide Association StudyLinkage DisequilibriumModels, GeneticPedigreePolymorphism, Single NucleotideAnimalsMice

Identifiers

PMID30677030
PMCPMC6345469
OpenAlexW2952824708

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.