Applications of Machine Learning and Data Mining Methods to Detect Associations of Rare and Common Variants with Complex Traits. Issue 1 (September 2014)
- Record Type:
- Journal Article
- Title:
- Applications of Machine Learning and Data Mining Methods to Detect Associations of Rare and Common Variants with Complex Traits. Issue 1 (September 2014)
- Main Title:
- Applications of Machine Learning and Data Mining Methods to Detect Associations of Rare and Common Variants with Complex Traits
- Authors:
- Lu, Ake Tzu‐Hui
Austin, Erin
Bonner, Ashley
Huang, Hsin‐Hsiung
Cantor, Rita M.
Paterson, Andrew
Bickeböller, Heike
Almasy, Laura - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Machine learning methods (MLMs), designed to develop models using high‐dimensional predictors, have been used to analyze genome‐wide genetic and genomic data to predict risks for complex traits. We summarize the results from six contributions to our Genetic Analysis Workshop 18 working group; these investigators applied MLMs and data mining to analyses of rare and common genetic variants measured in pedigrees. To develop risk profiles, group members analyzed blood pressure traits along with single‐nucleotide polymorphisms and rare variant genotypes derived from sequence and imputation analyses in large Mexican American pedigrees. Supervised MLMs included penalized regression with varying penalties, support vector machines, and permanental classification. Unsupervised MLMs included sparse principal components analysis and sparse graphical models. Entropy‐based components analyses were also used to mine these data. None of the investigators fully capitalized on the genetic information provided by the complete pedigrees. Their approaches either corrected for the nonindependence of the individuals within the pedigrees or analyzed only those who were independent. Some methods allowed for covariate adjustment, whereas others did not. We evaluated these methods using a variety of metrics. Four contributors conducted primary analyses on the real data, and the other two research groups used the simulated data with and without<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Machine learning methods (MLMs), designed to develop models using high‐dimensional predictors, have been used to analyze genome‐wide genetic and genomic data to predict risks for complex traits. We summarize the results from six contributions to our Genetic Analysis Workshop 18 working group; these investigators applied MLMs and data mining to analyses of rare and common genetic variants measured in pedigrees. To develop risk profiles, group members analyzed blood pressure traits along with single‐nucleotide polymorphisms and rare variant genotypes derived from sequence and imputation analyses in large Mexican American pedigrees. Supervised MLMs included penalized regression with varying penalties, support vector machines, and permanental classification. Unsupervised MLMs included sparse principal components analysis and sparse graphical models. Entropy‐based components analyses were also used to mine these data. None of the investigators fully capitalized on the genetic information provided by the complete pedigrees. Their approaches either corrected for the nonindependence of the individuals within the pedigrees or analyzed only those who were independent. Some methods allowed for covariate adjustment, whereas others did not. We evaluated these methods using a variety of metrics. Four contributors conducted primary analyses on the real data, and the other two research groups used the simulated data with and without knowledge of the underlying simulation model. One group used the answers to the simulated data to assess power and type I errors. Although the MLMs applied were substantially different, each research group concluded that MLMs have advantages over standard statistical approaches with these high‐dimensional data.</p> </abstract> … (more)
- Is Part Of:
- Genetic epidemiology. Volume 38:Issue 1(2014)
- Journal:
- Genetic epidemiology
- Issue:
- Volume 38:Issue 1(2014)
- Issue Display:
- Volume 38, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 38
- Issue:
- 1
- Issue Sort Value:
- 2014-0038-0001-0000
- Page Start:
- S81
- Page End:
- S85
- Publication Date:
- 2014-09
- Subjects:
- Genetic epidemiology -- Periodicals
Heredity -- Periodicals
Medical geography -- Periodicals
614 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2272 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/gepi.21830 ↗
- Languages:
- English
- ISSNs:
- 0741-0395
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4111.848000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4131.xml