Evidence map›Paper›PMID 29696245›Full record

ArticleResearch in computational molecular biology : ... Annual International Conference, RECOMB ... : proceedings. RECOMB (Conference : 2005- )2017

Longitudinal Genotype-Phenotype Association Study via Temporal Structure Auto-Learning Predictive Model.

Xiaoqian Wang, Jingwen Yan, Xiaohui Yao, Sungeun Kim, Kwangsik Nho, Shannon L Risacher, Andrew J Saykin, Li Shen, Heng Huang

Abstract read
In one paragraph

Article in Research in computational molecular biology : ... Annual International Conference, RECOMB ... : proceedings. RECOMB (Conference : 2005- ), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Xiaoqian WangComputer Science & Engineering, University of Texas at Arlington, TX, 76019, USA.
Jingwen YanRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Xiaohui YaoRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Sungeun KimRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Kwangsik NhoRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Shannon L RisacherRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Andrew J SaykinRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Li ShenRadiology & Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Heng HuangComputer Science & Engineering, University of Texas at Arlington, TX, 76019, USA.

Funding

Imaging Genomics Based Brain Disease PredictionR01AG049371 · NIA · UNIVERSITY OF TEXAS ARLINGTON · PI HUANG, HENG · 2015 to 2019
$2.0M
Integrating Neuroimaging, Multi-omics, and Clinical Data in Complex DiseaseR01LM012535 · NLM · INDIANA UNIVERSITY INDIANAPOLIS · PI NHO, KWANGSIK TIMOTHY · 2017 to 2021
$1.7M
Neurogenesis in Adult Brain: Gene Networks and Alzheimer’s DiseaseR03AG054936 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI NHO, KWANGSIK TIMOTHY · 2017 to 2018
$145k
NIA NIH HHS R01 AG049371NLM NIH HHS R01 LM012535
6 · The paper itself

Abstract

With rapid progress in high-throughput genotyping and neuroimaging, imaging genetics has gained significant attention in the research of complex brain disorders, such as Alzheimer's Disease (AD). The genotype-phenotype association study using imaging genetic data has the potential to reveal genetic basis and biological mechanism of brain structure and function. AD is a progressive neurodegenerative disease, thus, it is crucial to look into the relations between SNPs and longitudinal variations of neuroimaging phenotypes. Although some machine learning models were newly presented to capture the longitudinal patterns in genotype-phenotype association study, most of them required fixed longitudinal structures of prediction tasks and could not automatically learn the interrelations among longitudinal prediction tasks. To address this challenge, we proposed a novel temporal structure auto-learning model to automatically uncover longitudinal genotype-phenotype interrelations and utilized such interrelated structures to enhance phenotype prediction in the meantime. We conducted longitudinal phenotype prediction experiments on the ADNI cohort including 3,123 SNPs and 2 types of biomarkers, VBM and FreeSurfer. Empirical results demonstrated advantages of our proposed model over the counterparts. Moreover, available literature was identified for our top selected SNPs, which demonstrated the rationality of our prediction results. An executable program is available online at https://github.com/littleq1991/sparse_lowRank_regression.

Indexed as

Alzheimer’s DiseaseGenotype-Phenotype Association PredictionLongitudinal StudyLow-Rank ModelTemporal Structure Auto-Learning

Identifiers

PMID29696245
PMCPMC5912922

What Socratic holds

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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 Socratic graph.