General retrospective mega-analysis framework for rare variant association tests

Author:

Chien Li-Chu1ORCID,Chiu Yen-Feng2ORCID

Affiliation:

1. Center for Fundamental Science, Kaohsiung Medical University; Kaohsiung Taiwan, ROC

2. Institute of Population Health Sciences, National Health Research Institutes; Zhunan Taiwan, ROC

Funder

Ministry of Science and Technology, Taiwan

National Health Research Institutes

Ministry of Science and Technology

National Health Research Institutes (NHRI)

Publisher

Wiley

Subject

Genetics(clinical),Epidemiology

Reference47 articles.

1. Guidelines for large-scale sequence-based complex trait association studies: Lessons learned from the NHLBI exome sequencing Project;Auer;American Journal of Human Genetics,2016

2. Omics-squared: Human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19;Blangero;BMC Proceedings,2016

3. Common and rare variants in multifactorial susceptibility to common diseases;Bodmer;Nature Genetics,2008

4. Regulation of GPCR signaling in hypertension;Brinks;Biochimica et Biophysica Acta,2010

5. Combining cohorts in longitudinal surveys;Carrillo;Survey Methodology,2013

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