Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies-Reference-Cited by-同舟云学术

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Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies

Published:2019-05 Issue:5 Volume:104 Page:802-814
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Li Zilin,Li Xihao,Liu Yaowu,Shen Jincheng,Chen Han,Zhou Hufeng,Morrison Alanna C.,Boerwinkle Eric,Lin Xihong

Funder

National Heart, Lung, and Blood Institute

National Institutes of Health

Department of Health and Human Services

NIH

National Human Genome Research Institute

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference42 articles.

1. Five years of GWAS discovery;Visscher;Am. J. Hum. Genet.,2012

2. Finding the missing heritability of complex diseases;Manolio;Nature,2009

3. A map of human genome variation from population-scale sequencing;Abecasis;Nature,2010

4. Evolution and functional impact of rare coding variation from deep sequencing of human exomes;Tennessen;Science,2012

5. Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants;Fu;Nature,2013

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2. A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded protein;Human Genetics and Genomics Advances;2024-07

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4. FiMAP: A fast identity-by-descent mapping test for biobank-scale cohorts;PLOS Genetics;2023-12-01

5. Harnessing the Power of Statistics and Machine Learning in the Era of Biobank-Scale Whole-Genome Sequencing and Multi-Omics Studies;XRDS: Crossroads, The ACM Magazine for Students;2023-12

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