Association detection between ordinal trait and rare variants based on adaptive combination of P values. Issue 1 (January 2018)
- Record Type:
- Journal Article
- Title:
- Association detection between ordinal trait and rare variants based on adaptive combination of P values. Issue 1 (January 2018)
- Main Title:
- Association detection between ordinal trait and rare variants based on adaptive combination of P values
- Authors:
- Wang, Meida
Ma, Weijun
Zhou, Ying - Abstract:
- Abstract Next-generation sequencing technology not only presents a new method for the detection of human genomic structural variation, but also provides a large number of genetic data of rare variants for us. Currently, how to detect association between human complex diseases and rare variants using genetical data has attracted extensive attention. In the field of medicine, many people's health and disease conditions are measured by ordinal response variables, namely, the trait value reflects the development stage or severity of a certain condition. However, most existing methods to test for association between rare variants and complex diseases are designed to deal with dichotomous or quantitative traits. Association analysis methods of ordinal traits are relatively fewer, and considering ordinal traits as dichotomous and quantitative traits will inevitably lose some valuable information in the original data. Therefore, in this paper, we extend an existing method of adaptive combination ofP values (ADA) and propose a new method of association analysis for ordinal trait based on it (called OR-ADA) to test for possible association between ordinal trait and rare variants. In our method, we establish a cumulative logistic regression model, in which the regression coefficients are estimated by the Newton–Raphson algorithm and the likelihood ratio test is used to test the association. Through a large number of simulation studies and an example, we demonstrate the performance ofAbstract Next-generation sequencing technology not only presents a new method for the detection of human genomic structural variation, but also provides a large number of genetic data of rare variants for us. Currently, how to detect association between human complex diseases and rare variants using genetical data has attracted extensive attention. In the field of medicine, many people's health and disease conditions are measured by ordinal response variables, namely, the trait value reflects the development stage or severity of a certain condition. However, most existing methods to test for association between rare variants and complex diseases are designed to deal with dichotomous or quantitative traits. Association analysis methods of ordinal traits are relatively fewer, and considering ordinal traits as dichotomous and quantitative traits will inevitably lose some valuable information in the original data. Therefore, in this paper, we extend an existing method of adaptive combination ofP values (ADA) and propose a new method of association analysis for ordinal trait based on it (called OR-ADA) to test for possible association between ordinal trait and rare variants. In our method, we establish a cumulative logistic regression model, in which the regression coefficients are estimated by the Newton–Raphson algorithm and the likelihood ratio test is used to test the association. Through a large number of simulation studies and an example, we demonstrate the performance of the new method and compare it with several methods. The analysis results show that the OR-ADA strategy is robust to the signs of effects of causal variants and more powerful under many scenarios. … (more)
- Is Part Of:
- Journal of human genetics. Volume 63:Issue 1(2018)
- Journal:
- Journal of human genetics
- Issue:
- Volume 63:Issue 1(2018)
- Issue Display:
- Volume 63, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 63
- Issue:
- 1
- Issue Sort Value:
- 2018-0063-0001-0000
- Page Start:
- 37
- Page End:
- 45
- Publication Date:
- 2018-01
- Subjects:
- Medical genetics -- Periodicals
Human genetics -- Periodicals
616.042 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://www.nature.com/ ↗
http://link.springer-ny.com/link/service/journals/10038/index.htm ↗
http://www.nature.com/jhg/index.html ↗ - DOI:
- 10.1038/s10038-017-0354-2 ↗
- Languages:
- English
- ISSNs:
- 1434-5161
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5003.415500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11056.xml