Evidence map›Paper›PMID 26288029›Full record

ArticleBiometrics2016

Detection of gene-gene interactions using multistage sparse and low-rank regression.

Hung Hung, Yu-Ting Lin, Penweng Chen, Chen-Chien Wang, Su-Yun Huang, Jung-Ying Tzeng

Abstract read
In one paragraph

Article in Biometrics, 2016. 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
–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

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.

  1. Article
  2. Article
  3. Sparse and Low-rank Tensor Estimation via Cubic Sketchings.IEEE transactions on information theory · 2020
    Article
  4. Article
  5. Efficient Signal Inclusion With Genomic Applications.Journal of the American Statistical Association · 2019
    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

6 authors.

Hung HungInstitute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei 100, Taiwan.
Yu-Ting LinInstitute of Statistical Science, Academia Sinica, Taipei 115, Taiwan.
Penweng ChenDepartment of Applied Mathematics, National Chung Hsing University, Taichung 402, Taiwan.
Chen-Chien WangYahoo, Sunnyvale, California 94089, U.S.A.
Su-Yun HuangInstitute of Statistical Science, Academia Sinica, Taipei 115, Taiwan.
Jung-Ying TzengDepartment of Statistics and Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina 27695, U.S.A.

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
An integrative statistics-guided image-based multi-scale lung modelU01HL114494 · NHLBI · UNIVERSITY OF IOWA · PI LIN, CHING-LONG · 2013 to 2017
$3.1M
Genome-wide Haplotype Association Analysis in Mental DisordersR01MH084022 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TZENG, JUNG-YING · 2009 to 2011
$1.1M
NCI NIH HHS P01 CA142538NCI NIH HHS P01-CA-142538NHLBI NIH HHS U01 HL114494NHLBI NIH HHS U01-HL-114494NIMH NIH HHS R01 MH084022NIMH NIH HHS R01-MH-084 022
6 · The paper itself

Abstract

Finding an efficient and computationally feasible approach to deal with the curse of high-dimensionality is a daunting challenge faced by modern biological science. The problem becomes even more severe when the interactions are the research focus. To improve the performance of statistical analyses, we propose a sparse and low-rank (SLR) screening based on the combination of a low-rank interaction model and the Lasso screening. SLR models the interaction effects using a low-rank matrix to achieve parsimonious parametrization. The low-rank model increases the efficiency of statistical inference and, hence, SLR screening is able to more accurately detect gene-gene interactions than conventional methods. Incorporation of SLR screening into the Screen-and-Clean approach (Wasserman and Roeder, 2009; Wu et al., 2010) is also discussed, which suffers less penalty from Boferroni correction, and is able to assign p-values for the identified variables in high-dimensional model. We apply the proposed screening procedure to the Warfarin dosage study and the CoLaus study. The results suggest that the new procedure can identify main and interaction effects that would have been omitted by conventional screening methods.

Indexed as

AlgorithmsData Interpretation, StatisticalModels, StatisticalRegression AnalysisComputer SimulationHigh-Throughput Screening AssaysPattern Recognition, AutomatedProtein Interaction MappingReproducibility of ResultsSensitivity and SpecificityAsymptotic normalityGene-gene interactionsLow-rank approximationOver-parametrizationScreen-and-CleanSparsity

Identifiers

PMID26288029
PMCPMC4760921

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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.