Evidence map›Paper›PMID 39555004›Full record

ArticleComputational statistics & data analysis2023

Locally sparse quantile estimation for a partially functional interaction model.

Weijuan Liang, Qingzhao Zhang, Shuangge Ma

Abstract read
In one paragraph

Article in Computational statistics & data analysis, 2023. 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

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.

  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

3 authors.

Weijuan LiangSchool of Statistics, Renmin University of China, Beijing, China.
Qingzhao ZhangDepartment of Statistics and Data Science, School of Economics, The Wang Yanan Institute for Studies in Economics, and Fujian Key Lab of Statistics, Xiamen University, Xiamen, China.
Shuangge MaDepartment of Biostatistics, Yale School of Public Health, New Haven, CT, USA.

Funding

Novel methods for identifying genetic interactions in cancer prognosisR01CA204120 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2016 to 2026
$3.5M
NCI NIH HHS R01 CA204120
6 · The paper itself

Abstract

Functional data analysis has been extensively conducted. In this study, we consider a partially functional model, under which some covariates are scalars and have linear effects, while some other variables are functional and have unspecified nonlinear effects. Significantly advancing from the existing literature, we consider a model with interactions between the functional and scalar covariates. To accommodate long-tailed error distributions which are not uncommon in data analysis, we adopt the quantile technique for estimation. To achieve more interpretable estimation, and to accommodate many practical settings, we assume that the functional covariate effects are locally sparse (that is, there exist subregions on which the effects are exactly zero), which naturally leads to a variable/model selection problem. We propose respecting the "main effect, interaction" hierarchy, which postulates that if a subregion has a nonzero effect in an interaction term, then its effect has to be nonzero in the corresponding main functional effect. For estimation, identification of local sparsity, and respect of the hierarchy, we propose a penalization approach. An effective computational algorithm is developed, and the consistency properties are rigorously established under mild regularity conditions. Simulation shows the practical effectiveness of the proposed approach. The analysis of the Tecator data further demonstrates its practical applicability. Overall, this study can deliver a novel and practically useful model and a statistically and numerically satisfactory estimation approach.

Indexed as

Interaction analysisLocally sparse estimationPartially functional modelQuantile estimation

Identifiers

PMID39555004
PMCPMC11566403

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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.