Evidence map›Paper›PMID 31195980›Full record

ArticleBMC bioinformatics2019

fastJT: An R package for robust and efficient feature selection for machine learning and genome-wide association studies.

Jiaxing Lin, Alexander Sibley, Ivo Shterev, Andrew Nixon, Federico Innocenti, Cliburn Chan, Kouros Owzar

Abstract read
In one paragraph

Article in BMC bioinformatics, 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

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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

7 authors.

Jiaxing LinDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA.
Alexander SibleyDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Ivo ShterevDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, USA.
Andrew NixonDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Federico InnocentiDivision of Pharmacotherapy and Experimental Therapeutics, Chapel Hill, NC, USA.
Cliburn ChanDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA.
Kouros OwzarDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA. Kouros.Owzar@duke.edu.ORCID http://orcid.org/0000-0002-3340-1287

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVIDIAN, MARIE, KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
National Cancer Institute P01CA142538NCI NIH HHS P01 CA142538NIH HHS S10 OD018164
6 · The paper itself

Abstract

backgroundParametric feature selection methods for machine learning and association studies based on genetic data are not robust with respect to outliers or influential observations. While rank-based, distribution-free statistics offer a robust alternative to parametric methods, their practical utility can be limited, as they demand significant computational resources when analyzing high-dimensional data. For genetic studies that seek to identify variants, the hypothesis is constrained, since it is typically assumed that the effect of the genotype on the phenotype is monotone (e.g., an additive genetic effect). Similarly, predictors for machine learning applications may have natural ordering constraints. Cross-validation for feature selection in these high-dimensional contexts necessitates highly efficient computational algorithms for the robust evaluation of many features.

resultsWe have developed an R extension package, fastJT, for conducting genome-wide association studies and feature selection for machine learning using the Jonckheere-Terpstra statistic for constrained hypotheses. The kernel of the package features an efficient algorithm for calculating the statistics, replacing the pairwise comparison and counting processes with a data sorting and searching procedure, reducing computational complexity from O(n

conclusionsfastJT is an open-source R extension package, applying the Jonckheere-Terpstra statistic for robust feature selection for machine learning and association studies. The package implements an efficient algorithm which leverages internal information among the samples to avoid unnecessary computations, and incorporates shared-memory parallel programming to further boost performance on multi-core machines.

Indexed as

AlgorithmsGenome-Wide Association StudyMachine LearningBlood ProteinsComputer SimulationPolymorphism, Single NucleotideQuantitative Trait, HeritableBlood ProteinsConstrained inferenceFeature selectionGenome-wide association studiesJonckheere-TerpstraLinear rank statisticLogarithmic complexityMachine learningParallel processingRobust statistic

Identifiers

PMID31195980
PMCPMC6567636

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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.