On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows-Reference-Cited by-同舟云学术

On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows

Published:2017-03-20 Issue:4 Volume:41 Page:332-340
ISSN:0741-0395
Container-title:Genetic Epidemiology
language:en
Short-container-title:Genet. Epidemiol.

Author:

Loehlein Fier Heide¹²,Prokopenko Dmitry³,Hecker Julian²,Cho Michael H.³,Silverman Edwin K.³,Weiss Scott T.³,Tanzi Rudolph E.⁴,Lange Christoph¹³

Affiliation:

1. Department of Biostatistics; Harvard T.H. Chan School of Public Health; Boston Massachusetts United States of America

2. Working Group of Genomic Mathematics; University of Bonn; Bonn Germany

3. Channing Division of Network Medicine; Department of Medicine; Brigham and Women's Hospital; Harvard Medical School; Boston Massachusetts United States of America

4. Genetics and Aging Research Unit; MassGeneral Institute for Neurodegenerative Disease; Massachusetts General Hospital; Harvard Medical School; Charlestown Massachusetts United States of America

Funder

Cure Alzheimer's Fund

National Institute of Mental Health

National Heart, Lung, and Blood Institute

National Human Genome Research Institute

Deutsche Forschungsgemeinschaft

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Epidemiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gepi.22040/fullpdf

Reference33 articles.

1. A global reference for human genetic variation;1000 Genomes Project Consortium;Nature,2015

2. Rare variant analysis for family-based design;De;PloS One,2013

3. Evans , I. S. 1977 The selection of class intervals. Transactions of the Institute of British Geographers 98 124

4. Location, location, location’: A spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate;Fier;Bioinformatics,2012

5. On grouping for maximum homogeneity;Fisher;Journal of the American statistical Association,1958

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants;American Journal of Respiratory and Critical Care Medicine;2023-05-01

2. Spatial clustering analysis of green economy based on knowledge graph;Journal of Intelligent & Fuzzy Systems;2021-05-23

3. Whole‐genome sequencing reveals new Alzheimer's disease–associated rare variants in loci related to synaptic function and neuronal development;Alzheimer's & Dementia;2021-04-02

4. A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests;Bioinformatics;2020-12-01

5. Whole-genome sequencing reveals new Alzheimer’s disease-associated rare variants in loci related to synaptic function and neuronal development;2020-11-04