SimPEL: Simulation‐based power estimation for sequencing studies of low‐prevalence conditions. Issue 5 (22nd May 2018)
- Record Type:
- Journal Article
- Title:
- SimPEL: Simulation‐based power estimation for sequencing studies of low‐prevalence conditions. Issue 5 (22nd May 2018)
- Main Title:
- SimPEL: Simulation‐based power estimation for sequencing studies of low‐prevalence conditions
- Authors:
- Mak, Lauren
Li, Minghao
Cao, Chen
Gordon, Paul
Tarailo‐Graovac, Maja
Bousman, Chad
Wang, Pei
Long, Quan - Abstract:
- ABSTRACT: Power estimations are important for optimizing genotype‐phenotype association study designs. However, existing frameworks are designed for common disorders, and thus ill‐suited for the inherent challenges of studies for low‐prevalence conditions such as rare diseases and infrequent adverse drug reactions. These challenges include small sample sizes and the need to leverage genetic annotation resources in association analyses for the purpose of ranking potential causal genes. We present SimPEL, a simulation‐based program providing power estimations for the design of low‐prevalence condition studies. SimPEL integrates the usage of gene annotation resources for association analyses. Customizable parameters, including the penetrance of the putative causal allele and the employed pathogenic scoring system, allow SimPEL to realistically model a large range of study designs. To demonstrate the effects of various parameters on power, we estimated the power of several simulated designs using SimPEL and captured power trends in agreement with observations from current literature on low‐frequency condition studies. SimPEL, as a tool, provides researchers studying low‐frequency conditions with an intuitive and highly flexible avenue for statistical power estimation. The platform‐independent "batteries included" executable and default input files are available athttps://github.com/precisionomics/SimPEL .
- Is Part Of:
- Genetic epidemiology. Volume 42:Issue 5(2018)
- Journal:
- Genetic epidemiology
- Issue:
- Volume 42:Issue 5(2018)
- Issue Display:
- Volume 42, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 42
- Issue:
- 5
- Issue Sort Value:
- 2018-0042-0005-0000
- Page Start:
- 480
- Page End:
- 487
- Publication Date:
- 2018-05-22
- Subjects:
- adverse drug reactions -- association analyses -- genetic variant annotation -- genome‐wide sequencing -- power estimation -- rare disease
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.22129 ↗
- 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:
- 6899.xml