Evidence map›Paper›PMID 22150548›Full record

ArticleAnnals of human genetics2012

TRM: a powerful two-stage machine learning approach for identifying SNP-SNP interactions.

Hui-Yi Lin, Y Ann Chen, Ya-Yu Tsai, Xiaotao Qu, Tung-Sung Tseng, Jong Y Park

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In one paragraph

Article in Annals of human genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014
    Review
  8. Article
  9. 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.

Hui-Yi LinH. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA. ronnie.sebro@radiology.ucsf.edu
Y Ann Chen
Ya-Yu Tsai
Xiaotao Qu
Tung-Sung Tseng
Jong Y Park

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Genetic & epigenetic analysis of angiogenesis genes in recurrent prostate cancerR01CA128813 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PARK, JONG Y. · 2008 to 2012
$2.0M
NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA128813NCI NIH HHS R01CA128813
6 · The paper itself

Abstract

Studies have shown that interactions of single nucleotide polymorphisms (SNPs) may play an important role in understanding the causes of complex disease. We have proposed an integrated machine learning method that combines two machine-learning methods-Random Forests (RF) and Multivariate Adaptive Regression Splines (MARS)-to identify a subset of important SNPs and detect interaction patterns more effectively and efficiently. In this two-stage RF-MARS (TRM) approach, RF is first applied to detect a predictive subset of SNPs, and then MARS is used to identify the interaction patterns. We evaluated the TRM performances in four models. RF variable selection was based on out-of-bag classification error rate (OOB) and variable important spectrum (IS). Our results support that RF(OOB) had better performance than MARS and RF(IS) in detecting important variables. This study demonstrates that TRM(OOB) , which is RF(OOB) plus MARS, has combined the strengths of RF and MARS in identifying SNP-SNP interactions in a scenario of 100 candidate SNPs. TRM(OOB) had greater true positive rate and lower false positive rate compared with MARS, particularly for searching interactions with a strong association with the outcome. Therefore, the use of TRM(OOB) is favored for exploring SNP-SNP interactions in a large-scale genetic variation study.

Indexed as

Artificial IntelligenceModels, GeneticPolymorphism, Single NucleotideDecision TreesGenotypeHumansMaleModels, StatisticalProstatic NeoplasmsReceptors, EstrogenReceptors, Estrogen

Identifiers

PMID22150548
PMCPMC3243917

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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.