Evidence map›Paper›PMID 31985088›Full record

ArticleStatistics in medicine2020

Multikernel linear mixed model with adaptive lasso for complex phenotype prediction.

Yalu Wen, Qing Lu

Abstract read
In one paragraph

Article in Statistics in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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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

2 authors.

Yalu WenDepartment of Statistics, The University of Auckland, Auckland, New Zealand.ORCID 0000-0002-0071-5917
Qing LuDepartment of Epidemiology and Biostatistics, Michigan State University, East Lansing, Michigan.

Funding

Computational Efficient Statistical Tools for Analyzing Substance Dependence Sequencing DataR01DA043501 · NIDA · UNIVERSITY OF FLORIDA · PI LU, QING · 2017 to 2021
$2.1M
Methods and Software for High-dimensional Risk Prediction ResearchR01LM012848 · NLM · UNIVERSITY OF FLORIDA · PI LU, QING · 2018 to 2021
$1.2M
NIDA NIH HHS R01 DA043501NIDA NIH HHS R01DA043501NLM NIH HHS R01 LM012848U.S. National Library of Medicine R01LM012848
6 · The paper itself

Abstract

Linear mixed models (LMMs) and their extensions have been widely used for high-dimensional genomic data analyses. While LMMs hold great promise for risk prediction research, the high dimensionality of the data and different effect sizes of genomic regions bring great analytical and computational challenges. In this work, we present a multikernel linear mixed model with adaptive lasso (KLMM-AL) to predict phenotypes using high-dimensional genomic data. We develop two algorithms for estimating parameters from our model and also establish the asymptotic properties of LMM with adaptive lasso when only one dependent observation is available. The proposed KLMM-AL can account for heterogeneous effect sizes from different genomic regions, capture both additive and nonadditive genetic effects, and adaptively and efficiently select predictive genomic regions and their corresponding effects. Through simulation studies, we demonstrate that KLMM-AL outperforms most of existing methods. Moreover, KLMM-AL achieves high sensitivity and specificity of selecting predictive genomic regions. KLMM-AL is further illustrated by an application to the sequencing dataset obtained from the Alzheimer's disease neuroimaging initiative.

Indexed as

AlgorithmsGenomicsComputer SimulationLinear ModelsPhenotypeadaptive lassohigh-dimensional sequencing datalinear mixed modelrisk prediction

Identifiers

PMID31985088
PMCPMC8082466

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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.